Next Article in Journal
Correction of Fanconi Anemia Mutations Using Digital Genome Engineering
Next Article in Special Issue
Cancer Resistance to Immunotherapy: Molecular Mechanisms and Tackling Strategies
Previous Article in Journal
Facile Construction of Iron/Nickel Phosphide Nanocrystals Anchored on N-B-Doped Carbon-Based Composites with Advanced Catalytic Capacity for 4-Nitrophenol and Methylene Blue
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
IJMS
Volume 23
Issue 15
10.3390/ijms23158412
ijms-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

PARP Inhibitors: Clinical Limitations and Recent Attempts to Overcome Them

by
Dongha Kim
1 and
Hye Jin Nam
2,3,*
1
Department of Anatomy, College of Medicine, The Catholic University of Korea, Seoul 06591, Korea
2
Drug Discovery Platform Research Center, Therapeutics and Biotechnology Division, Korea Research Institute of Chemical Technology, Daejeon 34114, Korea
3
Department of Medicinal Chemistry and Pharmacology, University of Science and Technology, Daejeon 34113, Korea
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2022, 23(15), 8412; https://doi.org/10.3390/ijms23158412
Submission received: 6 July 2022 / Revised: 26 July 2022 / Accepted: 28 July 2022 / Published: 29 July 2022
(This article belongs to the Special Issue Drug Resistance in Cancer: Molecular Mechanisms and Tackling Strategies)
Browse Figures
Versions Notes

Abstract

:
PARP inhibitors are the first clinically approved drugs that were developed based on synthetic lethality. PARP inhibitors have shown promising outcomes since their clinical applications and have recently been approved as maintenance treatment for cancer patients with BRCA mutations. PARP inhibitors also exhibit positive results even in patients without homologous recombination (HR) deficiency. Therapeutic effects were successfully achieved; however, the development of resistance was unavoidable. Approximately 40–70% of patients are likely to develop resistance. Here, we describe the mechanisms of action of PARP inhibitors, the causes of resistance, and the various efforts to overcome resistance. Particularly, we determined the survival probability of cancer patients according to the expression patterns of genes associated with HR restoration, which are critical for the development of PARP inhibitor resistance. Furthermore, we discuss the innovative attempts to degrade PARP proteins by chemically modifying PARP inhibitors. These efforts would enhance the efficacy of PARP inhibitors or expand the scope of their usage.

1. PARP Inhibitors for Cancer Treatment

Poly (ADP-ribose) polymerases (PARPs) are members of related enzymes that catalyze the transfer of ADP-ribose to target proteins [1,2]. PARP1 and PARP2 are considered to play an important role in maintaining genomic stability by mediating DNA repair processes. Among the PARP families, PARP1 shows abundant expression compared to the others and is responsible for most of the cellular PAR formation [3]; therefore, most studies have focused on PARP1. In this review, we discuss the mechanism of action of PARP inhibitors and the introduction of a new direction of therapeutic development utilizing PARP inhibitors, one of the important targeted anticancer therapies.

1.1. Synthetic Lethality of PARP Inhibitors

DNA damage response (DDR) is pivotal for maintaining genome stability because DNA is continually damaged by exogenous or endogenous genotoxic stress. It is estimated that DNA damage occurs at approximately 10,000 events per cell per day [4]. If damaged DNA is not swiftly recognized and properly corrected, genomic integrity is disrupted and various diseases, such as cancer, can occur. The repair machinery is specifically recruited according to the lesion of DNA damage; however, there is sufficient interactivity and redundancy to displace if certain pathways are disturbed or inhibited.
PARPs recognize and bind to DNA damage and mediates poly(ADP-ribosyl)ation (also known as PARylation) of several target proteins, including itself. Auto-PARylation of PARPs recruits DNA-repair systems, such as XRCC1 and DNA ligase, and PARPs are dissociated from damaged DNA (Figure 1). PARPs are also involved in the base excision repair (BER) pathway [5]. The BER pathway involves removal of damaged bases by DNA glycosylase, cleavage of AP sites by AP endonuclease, replacement of the missing nucleotides by DNA polymerase β (POLβ), and ligation of the nicks by DNA ligase I (LIG1) or DNA ligase III (LIG3) [6]. Interestingly, PARPs are responsible for accelerating BER [7]. DNA double-strand breaks (DSB) are recognized by ATM or PARPs and are repaired through HR or non-homologous recombination (NHEJ) [8]. HR is an error-free repair process dependent upon the guidance of a homologous template, while NHEJ directly ligates the two broken DNA ends and often causes an alteration in the DNA sequences around the DSB sites. Persistent accumulation of incorrect repairs of DSBs destabilizes the genome and eventually leads to cell death.
Although PARPs are important for DDR and repair systems, the PARP1 knockout mouse model does not exhibit developmental defects or early onset of cancer. Continuous SSBs of DNA caused by PARP1 knockout lead to DSB, thus triggering the HR DNA repair system. In addition, induction of a compensatory DSB repair system or alternative role of PARP2 may explain the normal susceptibility of PARP1 knockout mice to cancer [9]. PARP1 is required for cellular recovery from DNA damage; therefore, DNA-damaging reagents can increase lethality when PARP1 is inhibited. Indeed, PARP1 knockout mice displayed hypersensitivity to gamma irradiation and alkylating reagents [9]. This concept supports combination therapy of PARP inhibitors.
BRCA1/2 proteins are involved in DNA DSB repair and plays an important role in accurate DNA repair through HR process. BRCA1/2 proteins are considered to be tumor suppressors. Numerous studies have revealed that mutations in BRCA1/2 result in genomic instability and a high risk of developing ovarian and breast cancers; a breast cancer risk of 57% (95% confidence interval (CI), 0.47–0.66) for BRCA1 and 49% (95% CI, 0.40–0.57) for BRCA2 mutation carriers; and ovarian cancer risk of 40% (95% CI, 0.35–0.46) for BRCA1 and 18% (95% CI, 0.13–0.23) for BRCA2 mutation carriers [10]. It has been reported that approximately 5–10% of breast or ovarian cancer patients carry the BRCA1/2 mutations [11]. Therefore, genetic testing has been increasing in individuals with a family history of breast or ovarian cancer. Prophylactic mastectomy and prophylactic oophorectomy are occasionally performed in individuals who have been identified with a BRCA1/2 mutation through genetic testing. Multiple cases have reported that preventive surgery significantly reduces the risk of cancer [12,13].
Although inhibition of PARPs themselves does not significantly affect cell lethality, it can be fatal to cell viability if cells do not proceed to an alternative DNA repair system. Based on these findings, the idea of applying PARP inhibitors as a single agent to cancer patients with HR deficiency, such as BRCA1/2 mutations, was derived. PARPs inhibition induces severe genomic instability in BRCA1/2-mutated cells, rendering the cells inviable [14,15], whereas PARPs inhibition does not affect normal cell viability. In other words, PARPs inhibition induces apoptosis when HR is defective. Two individual DNA repair pathways cooperate to maintain DNA integrity, and thus simultaneous inhibition of both pathways results in cell death, termed synthetic lethality, whereas inhibition of either pathway alone does not.

1.2. PARP Inhibitors from Bench to Bedside

Various attempts have been made to demonstrate the concept of a synthetic lethal interaction between PARPs inhibition and BRCA1/2 mutations in clinical trials. As PARPs use nicotinamide adenine dinucleotide (NAD+) as a substrate for processing PARylation, small-molecule nicotinamide analogs that compete with NAD+ to occupy the PARPs catalytic domain were initially used to prove the concept in preclinical assays [16].
Efforts to discover drugs have led to the development of clinically usable PARP inhibitors, including olaparib, veliparib, rucaparib, niraparib, talazoparib, and pamiparib (Figure 2 and Table 1) [16]. These PARP inhibitors interact with the NAD+ binding site. Enzymatic inactivation of PARPs and trapping of PARPs at damaged DNA are the mechanisms of action of PARP inhibitors [17].
In 2014, olaparib (Lynparza; AstraZeneca) was approved for use as a single reagent by the European Medicines Agency (EMA) in the European Union and by the USA Food and Drug Administration (FDA). The FDA and EMA approved olaparib for the treatment of patients with deleterious or suspected deleterious germline BRCA (gBRCA)-mutated advanced ovarian cancer who have been treated with three or more prior lines of chemotherapy [18]. Moreover, olaparib was approved for the maintenance treatment of adult patients with recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer, who had a complete or partial response to platinum-based chemotherapy in 2017 [19]. In 2018, olaparib was approved by the FDA for gBRCA mutated Her2-negative metastatic breast cancer. Among the PARP inhibitors, olaparib was the first to be approved for breast cancer treatment. In phase 3 clinical trials, the median progression-free survival (PFS) was significantly longer in the olaparib group than in the standard therapy group (7.0 months vs. 4.2 months; hazard ratio for disease progression or death, 0.58; 95% CI, 0.43–0.80) (OlympiAD trial, NCT02000622) [20]. As such, the clinical applications of olaparib have been increasing through various clinical trials and subsequent approvals. Notably, olaparib gained FDA approval in 2019 for the indication of pancreatic cancer (NCT02184195) [21]. Metastatic pancreatic cancer patients have been waiting for a long time for new therapeutic options. A phase 3 POLO trial (NCT02184195) showed that patients with a gBRCA mutation and metastatic pancreatic cancer that had not progressed during first-line platinum-based chemotherapy had significantly longer PFS with maintenance olaparib than with a placebo [21].
Rucaparib and niraparib (Zejula; GSK) have been approved for the treatment of ovarian cancer associated with HR deficiency. In addition, rucaparib has been approved for the treatment of patients with deleterious BRCA-mutated metastatic castrate-resistant prostate cancer (NCT02952534) [22]. Interestingly, the indications for niraparib were later expanded to patients with ovarian cancer regardless of their HR-deficient status. Significantly longer progression-free survival (PFS) in clinical trials (NCT02655016) led to FDA approval of niraparib as a maintenance therapy, regardless of biomarker status [23].
Veliparib (ABT-888; AbbVie) is undergoing phase 3 clinical trials as a combination therapy for breast, ovarian, and lung cancers. Although veliparib is an effective PARPs catalytic inhibitor with low IC50 values, its ability to trap PARPs is considered to be relatively weak [17]. However, veliparib increases sensitivity to treatments with DNA-damaging reagents, such as chemotherapy and radiation therapy [24]. A recent study reported that the median PFS in patients with gBRCA mutated and Her2-negative breast cancer increased when veliparib was added to carboplatine-paclitaxel treatment (veliparib: 16.6 months (95% CI 13.4–18.7) vs. control: 13.1 months (95% CI 11.4–14.5); NCT02163694) [25,26]. In addition, the combination with veliparib showed benefits in ovarian and lung cancers [27,28]. Interestingly, veliparib significantly improved the PFS of ovarian cancer patients regardless of the presence or absence of BRCA mutations or HR deficiency status, although the degree of benefit was higher in patients with HR deficiency [27]. Of note, this clinical trial included patients with BRCA1/2 somatic mutations.
Talazoparib (BMN 673/Talzenna; Pfizer) was approved for advanced breast cancer patients with gBRCA mutations [29]. Talazoparib is known to exhibit the most potent PARPs trapping ability. It has a more rigid structure and is the largest in size among the PARP inhibitors [24,30]. It is thought that the difference in chemical structure results in the difference in the PARPs trapping ability. Of note, the PARPs trapping mechanism is controversial. The mere inhibition of catalytic activity, which inhibits PARylation-dependent dissociation, might stabilize PARPs on DNA [31]. Because the efficacy of the preclinical data may not always translate directly into clinical effectiveness, efficacy comparisons between PARP inhibitors in clinics are required in the future.

2. PARP Inhibitors: Back to the Bench: PARPi Resistance

2.1. Reversion Mutations of HR Genes

Clinical trials have shown promising response rates in patients receiving PARP inhibitors; however, 40–70% of patients show a tendency to develop resistance over time. The molecular basis of acquired resistance has been increasingly elucidated. The most readily conceivable mechanism of PARP inhibitor resistance is the reversion mutation of BRCA1/2. In 2008, two independent research groups discovered BRCA reverse mutations that cause PARP inhibitor resistance [46,47]. Continuous exposure to PARP inhibitors or cisplatin ultimately resulted in resistance. Interestingly, it was confirmed that the protein-truncating c.6174delT frameshift mutation of BRCA2 in cancer cells was converted to restore the open reading frame (ORF). Functional recovery of BRCA2 proteins caused resistance to PARP inhibitors. BRCA2 functionality was restored only by acquiring certain functional domains, even if it was not fully converted to the wild type (WT). Therefore, mapping the consequences of reversion mutations on BRCA proteins can reveal which protein domains are functionally important in conferring resistance to treatment. In patients, the primary BRCA genes mutations are mostly insertions or deletions subsequent to frameshifts and stop codon acquisitions. BRCA1 primary mutations are predominantly located in the RING or BRCT domains [48], and BRCA2 primary mutations are located in BRC repeats or the N-terminus [48]. Secondary reversion mutations occur where the primary mutation causes a frameshift and restores the ORF through new mutations. It is known that the BRCA1 RING domain functions as an E3 ligase when bound to BARD1, and the BRCT domain is critical for binding with phosphorylated proteins. Additionally, the BRCT domain is critical for the stabilization and nuclear localization of the BRCA1 protein [49]. BRCA2 binds with RAD51 recombinase, which is important for HR repair, through BRC repeats. Intriguingly, there have been no reports on reversion mutations in which all BRC repeats have been completely eliminated, suggesting that minimal BRC is required to restore resistance in conferring BRCA2 function [48]. However, some cancers without BRCA mutations are still sensitive to PARP inhibitors [50,51,52], suggesting that various other components are intricately involved in the HR process.
In addition to BRCA reversion, secondary mutations of RAD51C and RAD51D were identified in patients administered rucaparib [53]. Interestingly, these mutations restored the function of RAD51 and increased resistance to PARP inhibitors [53]. These secondary mutations also cause clinical resistance to platinum-based chemotherapy.

2.2. Restoration of HR via Inactivation of Non-Homologous End Joining Proteins

Although both BRCA1/2 reversion mutations have been identified in patients, BRCA2 reversions are more frequently reported; approximately four times as many reversion mutations in BRCA2 have been reported in clinics [48]. This suggests that in the case of the BRCA1 mutation, there may be other mechanisms for inducing resistance to PARP inhibitors. BRCA1 is a pleiotropic DNA damage-responsive protein that is involved in both DNA repair and checkpoint activation, whereas BRCA2 is a mediator of the core mechanism of HR [54]. BRCA1 is responsible for multiple DDR steps—from the DNA damage sensor to the mediator, and finally to the repair effector. BRCA1 is phosphorylated by various checkpoint kinases, such as ATM, ATR, and CHK2, which regulate cell cycle checkpoints or facilitate DNA damage repair. In particular, BRCA1 functions upstream of BRCA2 in the BRCA1–BRCA2-mediated HR pathway [54]. Together, HR recovery and subsequent resistance induction in BRCA1-mutated cancers might be an outcome that bypasses multiple BRCA1-associated pathways.
BRCA1 is responsible for removing NHEJ proteins, such as p53-binding protein 1 (53BP1), from DSBs to prevent aberrant end-joining and to drive HR. Interestingly, in the absence of BRCA1, 53BP1 suppresses HR by limiting DNA end resection, which is critical for excessive NHEJ and subsequent apoptosis [55,56]. Therefore, it is exceedingly likely that 53BP1 inactivation affects the choice between NHEJ and HR, and, ultimately, the resistance. Indeed, loss of 53BP1 partially restores HR in BRCA1-deficient cells and develops resistance to PARP inhibitors [57]. Since 53BP1 expression is frequently lost in BRCA1/2-mutated or triple-negative breast cancers [58], it is thought that 53BP1 could be used as a biomarker for predicting the response of BRCA-mutated cancers to PARP inhibitor therapy. Consistently, 53BP1-negative breast cancer patients showed a poorer survival rate [58]. Loss of 53BP1 also develops resistance to DNA-damaging reagents, such as cisplatin and doxorubicin [57].
Loss of REV7/MAD2L2 also leads to HR restoration and subsequent PARP inhibitor resistance in BRCA1-deficient cells [59]. REV7/MAD2L2 is recruited to DNA damaged sites as a downstream of 53BP1 and blocks DNA resection to promote NHEJ [59]. Therefore, REV7/MAD2L2 depletion drives BRCA1-deficient cells to repair via HR pathways and renders them resistant to PARP inhibitors. The correlation of survival rates according to the degree of expression of REV7/MAD2L2 was investigated. The TCGA database was used to construct gene-specific survival probability panels for three types of cancers (pancreatic cancer, ovarian cancer, and breast cancer) where PARP inhibitors are predominantly used for treatment. High expression of REV7/MAD2L2 shows higher survival probabilities in pancreatic cancer (Figure 3A), ovarian cancer (Figure 3B), and breast cancer (Figure 3C), whereas low expression of REV7/MAD2L2 exhibits an unfavorable outcome (Figure 3).

2.3. Restoration of Replication Fork Stability

Timely and faithful duplication of the genome should be performed for genomic stability. Occasionally, impediments to the replication progress, such as DNA lesions or collisions with transcription machineries, lead to fork slowdown and/or stalling known as replication stress. PARP and BRCA play key roles in DNA replication, particularly for fork protection [60]. Multiple fork protection mechanisms, consisting of stabilization, repair, and restart processes, minimize genomic instability [60]. Paradoxically, these mechanisms are also active in cancer cells; however, they only serve to compromise the cytotoxicity caused by therapeutic agents. PARP inhibitors appear to increase replication fork speed and induce accumulated single-strand DNA damage and subsequent DSB [61]. These replication barriers caused by PARP inhibitors lead to fork stalling. BRCA proteins prevent the degradation of nascent DNA after replication stress; therefore, nascent DNA generated from stalled forks is degraded by MRE11 nuclease in BRCA-deficient cells, resulting in excessive genomic instability and apoptosis; that is, restoring fork stabilization in BRCA-deficient cells may be responsible for triggering PAPR inhibitor resistance, and a comprehensive understanding of how cells protect stalled forks could lead to the establishment of strategies to combat PARP inhibitor resistance in cancer treatment [55,60,62,63,64].
Interestingly, numerous studies have reported that restoring fork stabilization can render resistance to PARP inhibitors (Figure 4). Through impairment of MRE11 nuclease recruitment by MLL3/4 depletion, PTIP restores fork stability and drives resistance to PARP inhibitors [63]. Inactivation of SNF2-family fork remodelers, including SMARCAL1, ZRANB3, and HLTF, which are critical for fork reversal, reduces replication stress and genomic instability, and provides PARP inhibitor resistance [64]. RADX (CXorf57), a single-stranded DNA-binding protein, regulates RAD51 activity. RADX depletion restores fork protection in BRCA mutant cells and induces PARP inhibitor resistance [65]. Consistently, studies using BRCA-mutated cells with low expression of PTIP, RADX, and SMARCAL-1 showed poorer survival outcomes in a xenograft mouse model [60,63,64,65]. We also constructed survival probability panels for these genes using the TCGA database. In pancreatic cancer, similar to REV7/MAD2L2, low expression of ZRANB3 and HLTF shows poorer survival probabilities than those with high expression (Figure 5A,B). In ovarian cancer, low expression of SMARCAL-1 and PTIP exhibits an unfavorable outcome (Figure 5C,D). PTIP also shows similar survival probabilities in breast cancer (Figure 5E). FANCD2 overexpression confers resistance to PARP inhibitors through fork stabilization, suggesting that FANCD2 can be used as a biomarker for PARP inhibitors sensitivity [62]. Indeed, high expression of FANCD2 shows a lower survival probability in pancreatic cancer (Figure 5F). Surprisingly, stalled fork stabilization conferred resistance to PARP inhibitors and to chemotherapy such as cisplatin. As mentioned above, HR restoration also conferred resistance to chemotherapy. Taken together, these results suggest that resistance can be acquired through alteration of the DNA repair system in the case of DNA damage-related therapeutics.

2.4. PARP Mutations

PARP inhibitors target PARP proteins; therefore, the alteration of the PARP protein itself might lead to resistance. Mutation or depletion of target proteins can affect resistance to PARP inhibitors. PARP1 knockout cells were highly resistant to olaparib treatment [17], suggesting that PARP1 loss might lead to resistance. Genome-wide CRISPR–Cas9 mutagenesis screening identified several mutations in PARP1 that are related to PARP inhibitor resistance [66]. PARP1 mutations located in the DNA-binding ZnF domain failed to be recruited to the DNA damage site and did not produce PAR at damaged sites. Interestingly, ovarian cancer patients with the PARP1 p.R591C mutation (c.1771C>T) showed de novo resistance to olaparib, suggesting that this is partly validated in clinics as a mechanism of resistance to PARP inhibitors. Although the p.R591C mutation is not located in the ZnF domain, the dissociation rate from the damage sites is more rapid than that of WT.

3. Lessons from Bench: How Can We Overcome Resistance to PARPi or Expand the Use of PARPi?

3.1. PARPi Combination Approaches

Combination with inhibitors of particular cell cycle checkpoint kinases can enhance PAPR inhibitor sensitivity. Replication stress activates multiple cell cycle checkpoint kinases. The kinase ATR primarily recognizes a stalled replication fork and phosphorylates downstream signaling cascades, including BRCA1, Mec1, and 53BP1. Activated ATR induces a shutdown of origin firing and lowers fork speed through the activation of CHK1 and inactivation of CDK1/2 [67,68,69]. WEE1 kinases phosphorylate CDK1/2 to maintain their inactivation [70]. In other words, activation of ATM and WEE1 contributes to the maintenance of genomic stability in normal cells. ATR kinase plays a unique role in PARP inhibitor-resistant cells [55]. In PARP inhibitor-resistant BRCA1-deficient cells, ATR regulates both BRCA1-independent HR and fork protection by promoting RAD51 recruitment to DSBs and stalled forks [55]. These results indicate that PARP inhibitor resistance in BRCA1-deficient cancers might be overcome by co-treatment with an ATR inhibitor. Based on these results, phase 2 clinical trials of combination therapy with an ATR inhibitor (AZD6738) and olaparib for solid cancers, such as renal, pancreatic, and breast cancers (NCT03682289, NCT03330847), are ongoing. In a similar context, WEE1 inhibitors have emerged as promising alternatives, and various clinical trials are underway to evaluate their efficacy. Among them, phase 1 clinical trials are recruiting advanced solid cancer patients with selective mutations (BRCA1, BRCA2, BRIP1, FANCA, PALB2, or non-DDR gene markers) and PARP resistance (NCT04197713, STAR study). We anticipate that the results of overcoming PARP inhibitor resistance by WEE1 inhibitor (adavosertib/AZD1775) will be reproduced in a clinical setting.
Blocking CTLA4, PD-1, and PD-L1 immune checkpoints have emerged as new targets in cancer therapy, and these therapies have shown remarkable positive clinical effects. Interestingly, PARP inhibitor treatment upregulated PD-L1 expression in breast cancer cells, which weakened the efficacy of PARP inhibitors in terms of anti-cancer immunity [71]. An in vivo study showed that the combination of PARP inhibitors and anti-PD-L1 therapy significantly increased the therapeutic efficacy [71]. Currently, phase 2 clinical trials using olaparib and anti-PD-L1 (durvalumab or atezolizumab) combination for ovarian, breast, and gastric cancers (NCT02734004, NCT02849496) are ongoing.
Combination with inhibitors against restoration of PARylation can enhance PAPR inhibitor sensitivity. It has been reported that PARP1 phosphorylation at Tyr907 by c-Met increases PARylation activity of PARP1 and renders cancer cells resistant to PARP inhibitor [72]; that is, pY907 PARP1 might be a predictive marker for PARP inhibitor resistance. Indeed, the combination of c-Met and PARP1 inhibitors reduced tumor growth compared to either inhibitor alone. Loss of PAR glycohydrolase (PARG) is also related to restoration of PARylation. PARG degrades PAR by hydrolyzing the ribose–ribose bonds in poly(ADP-ribose) [73]. PARG knockdown partially restored PARylation despite PARP inhibitor treatment and resulted in PARP inhibitor resistance [50]. Interestingly, alteration of PAR signaling by downregulation of PARG increases the sensitivity to IR [50,52]. These studies suggest that assessment of PARG or c-Met activation is required to establish an appropriate therapeutic strategy.
Together, combination therapies to overcome PARP inhibitor resistance and enhance PARP inhibitor sensitivity are still in their infancy and have a long way to go. An increasing number of studies are required to investigate its feasibility in clinical settings.

3.2. Chemical Modifications of PARP Inhibitors

Researchers have attempted to develop more potent and broadly useful PARP inhibitors. Recently, chemically mediated targeted protein degradation has emerged as a promising and innovative technology for the development of new therapeutic drugs. Removal of targeted protein degradation through the ubiquitin proteasome system or autophagy generally provides a more potent inhibitory ability. The most well-known modulation methods are proteolysis-targeting chimeras (PROTAC) and hydrophobic tagging. PROTAC has the advantage of being easy to target intracellularly. Furthermore, it can be used to develop a therapeutic agent for intractable diseases because it can remove disease proteins that conventional antibody therapeutics have not been able to access.
Recently, the clinical application of the PROTAC method for cancer treatment has been attempted in various ways. In the second half of 2020, three PROTAC-related companies were listed in the US, with Arvinas announcing the positive results of their phase 1 clinical pipeline in December 2020, raising interest in PROTAC-related anticancer drugs [74]. In 2019, clinical trials were sequentially initiated for ARV-110, a metastatic castration-resistant prostate cancer treatment, and ARV-471, a locally advanced or metastatic ER-positive/HER2-negative breast cancer treatment. In addition, in October 2019, the initial safety and pharmacokinetic data of ARV-110 and ARV-471 were published (NCT03888612, NCT04072952). Recently, Arvinas announced the interim results of a phase 1 clinical trial and reported that the safety and tolerability problems of PROTAC were solved to a certain extent. However, it is still in the early stages of clinical research; therefore, it is necessary to broaden the scope of applied research, such as targeting PARP and PARP inhibitors.
To develop PARP-targeting PROTAC, a PARP inhibitor was connected to the E3 ubiquitin ligase ligand through a flexible linker (Figure 6). This bivalent molecule brings the E3 ligase and PARPs into close proximity, where PARPs are ubiquitinated and subsequently degraded through the proteasome pathway. Although more than 600 E3 ligases are expressed in mammalian cells, only limited E3 ligases (e.g., MDM2, cIAP1, cereblon [CRBN], VHL, RNF4, RNF14, and DCAF16) are used for PROTAC [75]. The choice of pairing E3 and PARP binders appears to be critical for the successful degradation of target proteins by PROTAC. In addition, the linker length should be optimized to allow ternary complex formation between E3 ligase and target proteins [76]. PROTACs using olaparib, rucaparib, and niraparib derivatives were developed and tested in cancer and non-cancer cells (Table 2). They showed superior cytotoxicity compared to that of conventional inhibitors and a wider range of uses beyond BRCA mutant cancers [77,78,79]. Among them, PROTAC using niraparib and MDM2 ligand exhibited PARP1 degradation and also increased PARP cleavage in MDA-MB-231 breast cancer cells. An interesting study was conducted to uncouple PARP1 catalytic inhibition and PARP1 trapping through the development of PARP PROTAC [80,81]. As mentioned above, PARP inhibitors can inhibit catalytic activity and induce PARPs trapping. PROTAC using rucaparib and CRBN ligand (iRucaparib-AP6) selectively degraded PARP1 and inhibited PARylation-mediated signaling events [81]. Interestingly, iRucaparib-AP6 did not induce PARP1 trapping or cell death in cardiomyocytes. Non-trapping PARP degraders are expected to be useful for the treatment of diseases associated with PARP activation (e.g., ischemia–reperfusion injury or neurodegenerative disease) because it does not induce genotoxicity or cell death.
Hydrophobic-tagging technology consists of a hydrophobic fragment (e.g., adamantyl, Boc3Arg, or fluorene) and a ligand for the targeted protein. Hydrophobic tagging mimics a partially unfolded or misfolded protein state and induces protein destabilization, thereby recruiting an endogenous chaperone protein to a hydrophobic-tagged protein and then degrading the targeted protein by the proteasome (Figure 6). Hydrophobic-tagged olaparib showed enhanced apoptosis in MBA-MB-231 cells, which are triple-negative breast cancer cells and carry the BRCA WT [82]. Interestingly, hydrophobic-tagged olaparib triggered the unfolded protein response (UPR) and endoplasmic reticulum (ER) stress. Excessive and irreversible UPR and ER stress-mediated apoptosis by hydrophobic tagging might be a mechanism of action that has better antitumor effects than olaparib in TNBC cells.
Hybrid drugs (also known as single-molecule multiple targets) also provide synergistic effects in treatment. Hybrid drugs are obtained by connecting two or more bioactive molecules [83,84]. Hybrid drugs have been developed based on combination therapies that overcome resistance or show improved outcomes, and their efficacy has been evaluated in preclinical studies (Figure 7).
As several BRCA1-related breast cancers are associated with activation of PI3K signaling [85], dual inhibitors targeting PARP and PI3K can be a promising strategy for cancer treatment. Based on this concept, dual inhibitors targeting PARP and PI3K were developed, and a more enhanced dual targeting capability was observed in cell-based assays [86]. Interestingly, dual inhibitors were found to be more efficacious than single administration of olaparib or BKM120 (PI3K inhibitor) and combined administration of olaparib and PI3K inhibitor in xenograft mouse models [86]. As co-treatment with HDAC inhibitors and PARP inhibitors exhibited synergistic effects in various cancer cells [87,88], researchers developed drugs that can simultaneously target PARP and HDAC. Dual PARP and HDAC inhibitors showed excellent inhibitory activities against PARP and HDAC and induced apoptosis in breast cancer cells [89]. DNA topoisomerases are involved in resolving the topological issues caused during replication or transcription [90]. Since both PARP inhibitors and topoisomerase I/II inhibitors are involved in replication fork stabilization, combinatorial inhibition of both target proteins may help overcoming resistance. Dual PARP and topoisomerase inhibitors showed significant anti-tumor activity without adverse toxicity in xenograft mouse models [91]. Hybrid inhibitors of PARP and PD-L1 were also developed by researchers. It has been reported that anti-tumor activity is improved when a PARP inhibitor is combined with a PD-1 antibody (pembrolizumab). In addition, PARP inhibitor treatment has been reported to upregulate PD-L1 expression in some cancer cells [92]. The dual inhibitors not only showed anti-tumor activity but also attenuated PD-L1 expression compared to the PARP inhibitor alone [93].

4. Concluding Remarks

Extensive efforts have been made to develop efficient PARP inhibitors, and drugs with high efficacy and tolerable toxicity have been actively used in clinics. Indeed, PARPs are undoubtedly an excellent drug target applicable to patients with BRCA mutations, and its scope of application is currently being extended. However, the occurrence of resistance is inevitable owing to the inherent limitations of targeted therapy. As seen above, except for the reversion mutation of BRCA, it appears that certain clues have been identified that show resistance can be overcome through preclinical assays, although clinical evidence is still lacking.
Although combination approaches that identify the mechanism of resistance and provide solutions are the forerunners, it is thought that the development of more creative and newer concepts of PARP inhibitors is required to prepare for unexpected situations in the future. The application of new technologies such as PROTAC or hydrophobic tagging to existing inhibitors is an impressive endeavor, although it is still in its infancy. As degrader technology continues to mature and be optimized, promising results are expected to be achieved in the near future. The development of structurally diverse inhibitors may be another option. To date, the majority of PARP inhibitors are NAD+ competitors, and their mechanism of action is almost similar. A recent study suggested structurally new non-NAD-like inhibitors and showed greater efficacy and potency than classical PARP inhibitors [94]. If innovative explorations are continuously performed and accumulated, potent drugs with new mechanisms are expected to be developed and used for patients.

Author Contributions

D.K. and H.J.N. conceived, wrote, and revised the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by a grant from the Bio & Medical Technology Development Program of the National Research Foundation (NRF), which is funded by the Ministry of Science and ICT (2020M3A9I4036072) to H.J.N; Basic Research Program of the NRF, which is funded by the Ministry of Science and ICT (2022R1A2C4002022) to D.K.; Basic Research Laboratory Program of the NRF, which is funded by the Ministry of Science and ICT (2021R1A4A3031875) to D.K.; The financial support of the Catholic Medical Center Research Foundation made in the program year of 2021 to D.K.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Amé, J.C.; Spenlehauer, C.; de Murcia, G. The PARP superfamily. BioEssays News Rev. Mol. Cell. Dev. Biol. 2004, 26, 882–893. [Google Scholar] [CrossRef]
  2. D’Amours, D.; Desnoyers, S.; D’Silva, I.; Poirier, G.G. Poly(ADP-ribosyl)ation reactions in the regulation of nuclear functions. Biochem. J. 1999, 342 Pt 2, 249–268. [Google Scholar] [CrossRef] [PubMed]
  3. Ray Chaudhuri, A.; Nussenzweig, A. The multifaceted roles of PARP1 in DNA repair and chromatin remodelling. Nat. Rev. Mol. Cell Biol. 2017, 18, 610–621. [Google Scholar] [CrossRef]
  4. Sandhu, S.K.; Yap, T.A.; de Bono, J.S. Poly(ADP-ribose) polymerase inhibitors in cancer treatment: A clinical perspective. Eur. J. Cancer 2010, 46, 9–20. [Google Scholar] [CrossRef] [PubMed]
  5. Kutuzov, M.M.; Belousova, E.A.; Kurgina, T.A.; Ukraintsev, A.A.; Vasil’eva, I.A.; Khodyreva, S.N.; Lavrik, O.I. The contribution of PARP1, PARP2 and poly(ADP-ribosyl)ation to base excision repair in the nucleosomal context. Sci. Rep. 2021, 11, 4849. [Google Scholar] [CrossRef]
  6. Izumi, T.; Mellon, I. Base Excision Repair and Nucleotide Excision Repair. In Genome Stability; Elsevier: Amsterdam, The Netherlands, 2021; pp. 293–322. [Google Scholar]
  7. Demin, A.A.; Hirota, K.; Tsuda, M.; Adamowicz, M.; Hailstone, R.; Brazina, J.; Gittens, W.; Kalasova, I.; Shao, Z.; Zha, S.; et al. XRCC1 prevents toxic PARP1 trapping during DNA base excision repair. Mol. Cell 2021, 81, 3018–3030.e5. [Google Scholar] [CrossRef] [PubMed]
  8. Nakamura, K.; Kustatscher, G.; Alabert, C.; Hodl, M.; Forne, I.; Volker-Albert, M.; Satpathy, S.; Beyer, T.E.; Mailand, N.; Choudhary, C.; et al. Proteome dynamics at broken replication forks reveal a distinct ATM-directed repair response suppressing DNA double-strand break ubiquitination. Mol. Cell 2021, 81, 1084–1099.e6. [Google Scholar] [CrossRef]
  9. Shall, S.; de Murcia, G. Poly (ADP-ribose) polymerase-1: What have we learned from the deficient mouse model? Mutat. Res./DNA Repair 2000, 460, 1–15. [Google Scholar] [CrossRef]
  10. Chen, S.; Parmigiani, G. Meta-analysis of BRCA1 and BRCA2 penetrance. J. Clin. Oncol. 2007, 25, 1329–1333. [Google Scholar] [CrossRef] [Green Version]
  11. Narod, S.A.; Foulkes, W.D. BRCA1 and BRCA2: 1994 and beyond. Nat. Rev. Cancer 2004, 4, 665–676. [Google Scholar] [CrossRef]
  12. Rebbeck, T.R.; Friebel, T.; Lynch, H.T.; Neuhausen, S.L.; van’t Veer, L.; Garber, J.E.; Evans, G.R.; Narod, S.A.; Isaacs, C.; Matloff, E.; et al. Bilateral prophylactic mastectomy reduces breast cancer risk in BRCA1 and BRCA2 mutation carriers: The PROSE Study Group. J. Clin. Oncol. 2004, 22, 1055–1062. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Rebbeck, T.R.; Lynch, H.T.; Neuhausen, S.L.; Narod, S.A.; Van’t Veer, L.; Garber, J.E.; Evans, G.; Isaacs, C.; Daly, M.B.; Matloff, E. Prophylactic oophorectomy in carriers of BRCA1 or BRCA2 mutations. N. Engl. J. Med. 2002, 346, 1616–1622. [Google Scholar] [CrossRef] [PubMed]
  14. Farmer, H.; McCabe, N.; Lord, C.J.; Tutt, A.N.; Johnson, D.A.; Richardson, T.B.; Santarosa, M.; Dillon, K.J.; Hickson, I.; Knights, C.; et al. Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy. Nature 2005, 434, 917–921. [Google Scholar] [CrossRef] [PubMed]
  15. Bryant, H.E.; Schultz, N.; Thomas, H.D.; Parker, K.M.; Flower, D.; Lopez, E.; Kyle, S.; Meuth, M.; Curtin, N.J.; Helleday, T. Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase. Nature 2005, 434, 913–917. [Google Scholar] [CrossRef]
  16. Lord, C.J.; Ashworth, A. PARP inhibitors: Synthetic lethality in the clinic. Science 2017, 355, 1152–1158. [Google Scholar] [CrossRef]
  17. Murai, J.; Huang, S.Y.; Das, B.B.; Renaud, A.; Zhang, Y.; Doroshow, J.H.; Ji, J.; Takeda, S.; Pommier, Y. Trapping of PARP1 and PARP2 by Clinical PARP Inhibitors. Cancer Res. 2012, 72, 5588–5599. [Google Scholar] [CrossRef] [Green Version]
  18. Kim, G.; Ison, G.; McKee, A.E.; Zhang, H.; Tang, S.; Gwise, T.; Sridhara, R.; Lee, E.; Tzou, A.; Philip, R.; et al. FDA Approval Summary: Olaparib Monotherapy in Patients with Deleterious Germline BRCA-Mutated Advanced Ovarian Cancer Treated with Three or More Lines of Chemotherapy. Clin. Cancer Res. 2015, 21, 4257–4261. [Google Scholar] [CrossRef] [Green Version]
  19. Ledermann, J.A.; Pujade-Lauraine, E. Olaparib as maintenance treatment for patients with platinum-sensitive relapsed ovarian cancer. Ther. Adv. Med. Oncol. 2019, 11, 1758835919849753. [Google Scholar] [CrossRef] [PubMed]
  20. Robson, M.; Im, S.A.; Senkus, E.; Xu, B.; Domchek, S.M.; Masuda, N.; Delaloge, S.; Li, W.; Tung, N.; Armstrong, A.; et al. Olaparib for Metastatic Breast Cancer in Patients with a Germline BRCA Mutation. N. Engl. J. Med. 2017, 377, 523–533. [Google Scholar] [CrossRef]
  21. Golan, T.; Hammel, P.; Reni, M.; Van Cutsem, E.; Macarulla, T.; Hall, M.J.; Park, J.O.; Hochhauser, D.; Arnold, D.; Oh, D.Y.; et al. Maintenance Olaparib for Germline BRCA-Mutated Metastatic Pancreatic Cancer. N. Engl. J. Med. 2019, 381, 317–327. [Google Scholar] [CrossRef]
  22. Anscher, M.S.; Chang, E.; Gao, X.; Gong, Y.; Weinstock, C.; Bloomquist, E.; Adeniyi, O.; Charlab, R.; Zimmerman, S.; Serlemitsos-Day, M.; et al. FDA Approval Summary: Rucaparib for the Treatment of Patients with Deleterious BRCA-Mutated Metastatic Castrate-Resistant Prostate Cancer. Oncologist 2021, 26, 139–146. [Google Scholar] [CrossRef]
  23. Mirza, M.R.; Monk, B.J.; Herrstedt, J.; Oza, A.M.; Mahner, S.; Redondo, A.; Fabbro, M.; Ledermann, J.A.; Lorusso, D.; Vergote, I.; et al. Niraparib Maintenance Therapy in Platinum-Sensitive, Recurrent Ovarian Cancer. N. Engl. J. Med. 2016, 375, 2154–2164. [Google Scholar] [CrossRef] [PubMed]
  24. Boussios, S.; Karihtala, P.; Moschetta, M.; Abson, C.; Karathanasi, A.; Zakynthinakis-Kyriakou, N.; Ryan, J.E.; Sheriff, M.; Rassy, E.; Pavlidis, N. Veliparib in ovarian cancer: A new synthetically lethal therapeutic approach. Investig. New Drugs 2020, 38, 181–193. [Google Scholar] [CrossRef] [PubMed]
  25. Arun, B.K.; Han, H.S.; Kaufman, B.; Wildiers, H.; Friedlander, M.; Ayoub, J.P.; Puhalla, S.L.; Bell-McGuinn, K.M.; Bach, B.A.; Kundu, M.G.; et al. Efficacy and safety of first-line veliparib and carboplatin-paclitaxel in patients with HER2- advanced germline BRCA+ breast cancer: Subgroup analysis of a randomised clinical trial. Eur. J. Cancer 2021, 154, 35–45. [Google Scholar] [CrossRef] [PubMed]
  26. Diéras, V.; Han, H.S.; Kaufman, B.; Wildiers, H.; Friedlander, M.; Ayoub, J.-P.; Puhalla, S.L.; Bondarenko, I.; Campone, M.; Jakobsen, E.H.; et al. Veliparib with carboplatin and paclitaxel in BRCA-mutated advanced breast cancer (BROCADE3): A randomised, double-blind, placebo-controlled, phase 3 trial. Lancet Oncol. 2020, 21, 1269–1282. [Google Scholar] [CrossRef]
  27. Coleman, R.L.; Fleming, G.F.; Brady, M.F.; Swisher, E.M.; Steffensen, K.D.; Friedlander, M.; Okamoto, A.; Moore, K.N.; Efrat Ben-Baruch, N.; Werner, T.L.; et al. Veliparib with First-Line Chemotherapy and as Maintenance Therapy in Ovarian Cancer. N. Engl. J. Med. 2019, 381, 2403–2415. [Google Scholar] [CrossRef] [PubMed]
  28. Ramalingam, S.S.; Novello, S.; Guclu, S.Z.; Bentsion, D.; Zvirbule, Z.; Szilasi, M.; Bernabe, R.; Syrigos, K.; Byers, L.A.; Clingan, P. Veliparib in Combination With Platinum-Based Chemotherapy for First-Line Treatment of Advanced Squamous Cell Lung Cancer: A Randomized, Multicenter Phase III Study. J. Clin. Oncol. 2021, 39, 3633–3644. [Google Scholar] [CrossRef]
  29. Litton, J.K.; Rugo, H.S.; Ettl, J.; Hurvitz, S.A.; Goncalves, A.; Lee, K.H.; Fehrenbacher, L.; Yerushalmi, R.; Mina, L.A.; Martin, M.; et al. Talazoparib in Patients with Advanced Breast Cancer and a Germline BRCA Mutation. N. Engl. J. Med. 2018, 379, 753–763. [Google Scholar] [CrossRef]
  30. Pommier, Y.; O’Connor, M.J.; De Bono, J. Laying a trap to kill cancer cells: PARP inhibitors and their mechanisms of action. Sci. Transl. Med. 2016, 8, 362ps317. [Google Scholar] [CrossRef]
  31. Kruger, A.; Burkle, A.; Hauser, K.; Mangerich, A. Real-time monitoring of PARP1-dependent PARylation by ATR-FTIR spectroscopy. Nat. Commun. 2020, 11, 2174. [Google Scholar] [CrossRef] [PubMed]
  32. Kaufman, B.; Shapira-Frommer, R.; Schmutzler, R.K.; Audeh, M.W.; Friedlander, M.; Balmana, J.; Mitchell, G.; Fried, G.; Stemmer, S.M.; Hubert, A.; et al. Olaparib monotherapy in patients with advanced cancer and a germline BRCA1/2 mutation. J. Clin. Oncol. 2015, 33, 244–250. [Google Scholar] [CrossRef] [PubMed]
  33. Ettl, J.; Quek, R.G.W.; Lee, K.H.; Rugo, H.S.; Hurvitz, S.; Goncalves, A.; Fehrenbacher, L.; Yerushalmi, R.; Mina, L.A.; Martin, M.; et al. Quality of life with talazoparib versus physician’s choice of chemotherapy in patients with advanced breast cancer and germline BRCA1/2 mutation: Patient-reported outcomes from the EMBRACA phase III trial. Ann. Oncol. 2018, 29, 1939–1947. [Google Scholar] [CrossRef] [PubMed]
  34. Oza, A.M.; Matulonis, U.A.; Malander, S.; Hudgens, S.; Sehouli, J.; del Campo, J.M.; Berton-Rigaud, D.; Banerjee, S.; Scambia, G.; Berek, J.S.; et al. Quality of life in patients with recurrent ovarian cancer treated with niraparib versus placebo (ENGOT-OV16/NOVA): Results from a double-blind, phase 3, randomised controlled trial. Lancet Oncol. 2018, 19, 1117–1125. [Google Scholar] [CrossRef]
  35. Del Campo, J.M.; Matulonis, U.A.; Malander, S.; Provencher, D.; Mahner, S.; Follana, P.; Waters, J.; Berek, J.S.; Woie, K.; Oza, A.M. Niraparib maintenance therapy in patients with recurrent ovarian cancer after a partial response to the last platinum-based chemotherapy in the ENGOT-OV16/NOVA trial. J. Clin. Oncol. 2019, 37, 2968. [Google Scholar] [CrossRef] [PubMed]
  36. Gonzalez-Martin, A.; Pothuri, B.; Vergote, I.; DePont Christensen, R.; Graybill, W.; Mirza, M.R.; McCormick, C.; Lorusso, D.; Hoskins, P.; Freyer, G.; et al. Niraparib in Patients with Newly Diagnosed Advanced Ovarian Cancer. N. Engl. J. Med. 2019, 381, 2391–2402. [Google Scholar] [CrossRef] [Green Version]
  37. Colombo, N.; Oza, A.M.; Lorusso, D.; Aghajanian, C.; Oaknin, A.; Dean, A.; Weberpals, J.I.; Clamp, A.R.; Scambia, G.; Leary, A.; et al. The effect of age on efficacy, safety and patient-centered outcomes with rucaparib: A post hoc exploratory analysis of ARIEL3, a phase 3, randomized, maintenance study in patients with recurrent ovarian carcinoma. Gynecol. Oncol. 2020, 159, 101–111. [Google Scholar] [CrossRef] [PubMed]
  38. Ledermann, J.A.; Oza, A.M.; Lorusso, D.; Aghajanian, C.; Oaknin, A.; Dean, A.; Colombo, N.; Weberpals, J.I.; Clamp, A.R.; Scambia, G.; et al. Rucaparib for patients with platinum-sensitive, recurrent ovarian carcinoma (ARIEL3): Post-progression outcomes and updated safety results from a randomised, placebo-controlled, phase 3 trial. Lancet Oncol. 2020, 21, 710–722. [Google Scholar] [CrossRef]
  39. Coleman, R.L.; Oza, A.M.; Lorusso, D.; Aghajanian, C.; Oaknin, A.; Dean, A.; Colombo, N.; Weberpals, J.I.; Clamp, A.; Scambia, G.; et al. Rucaparib maintenance treatment for recurrent ovarian carcinoma after response to platinum therapy (ARIEL3): A randomised, double-blind, placebo-controlled, phase 3 trial. Lancet 2017, 390, 1949–1961. [Google Scholar] [CrossRef] [Green Version]
  40. Poveda, A.; Floquet, A.; Ledermann, J.A.; Asher, R.; Penson, R.T.; Oza, A.M.; Korach, J.; Huzarski, T.; Pignata, S.; Friedlander, M.; et al. Olaparib tablets as maintenance therapy in patients with platinum-sensitive relapsed ovarian cancer and a BRCA1/2 mutation (SOLO2/ENGOT-Ov21): A final analysis of a double-blind, randomised, placebo-controlled, phase 3 trial. Lancet Oncol. 2021, 22, 620–631. [Google Scholar] [CrossRef]
  41. Tjokrowidjaja, A.; Lee, C.K.; Friedlander, M.; Gebski, V.; Gladieff, L.; Ledermann, J.; Penson, R.; Oza, A.; Korach, J.; Huzarski, T.; et al. Concordance between CA-125 and RECIST progression in patients with germline BRCA-mutated platinum-sensitive relapsed ovarian cancer treated in the SOLO2 trial with olaparib as maintenance therapy after response to chemotherapy. Eur. J. Cancer 2020, 139, 59–67. [Google Scholar] [CrossRef]
  42. Friedlander, M.; Gebski, V.; Gibbs, E.; Davies, L.; Bloomfield, R.; Hilpert, F.; Wenzel, L.B.; Eek, D.; Rodrigues, M.; Clamp, A.; et al. Health-related quality of life and patient-centred outcomes with olaparib maintenance after chemotherapy in patients with platinum-sensitive, relapsed ovarian cancer and a BRCA1/2 mutation (SOLO2/ENGOT Ov-21): A placebo-controlled, phase 3 randomised trial. Lancet Oncol. 2018, 19, 1126–1134. [Google Scholar] [CrossRef]
  43. Pujade-Lauraine, E.; Ledermann, J.A.; Selle, F.; Gebski, V.; Penson, R.T.; Oza, A.M.; Korach, J.; Huzarski, T.; Poveda, A.; Pignata, S.; et al. Olaparib tablets as maintenance therapy in patients with platinum-sensitive, relapsed ovarian cancer and a BRCA1/2 mutation (SOLO2/ENGOT-Ov21): A double-blind, randomised, placebo-controlled, phase 3 trial. Lancet Oncol. 2017, 18, 1274–1284. [Google Scholar] [CrossRef] [Green Version]
  44. Friedlander, M.; Moore, K.N.; Colombo, N.; Scambia, G.; Kim, B.-G.; Oaknin, A.; Lisyanskaya, A.; Sonke, G.S.; Gourley, C.; Banerjee, S.; et al. Patient-centred outcomes and effect of disease progression on health status in patients with newly diagnosed advanced ovarian cancer and a BRCA mutation receiving maintenance olaparib or placebo (SOLO1): A randomised, phase 3 trial. Lancet Oncol. 2021, 22, 632–642. [Google Scholar] [CrossRef]
  45. Moore, K.; Colombo, N.; Scambia, G.; Kim, B.G.; Oaknin, A.; Friedlander, M.; Lisyanskaya, A.; Floquet, A.; Leary, A.; Sonke, G.S.; et al. Maintenance Olaparib in Patients with Newly Diagnosed Advanced Ovarian Cancer. N. Engl. J. Med. 2018, 379, 2495–2505. [Google Scholar] [CrossRef]
  46. Sakai, W.; Swisher, E.M.; Karlan, B.Y.; Agarwal, M.K.; Higgins, J.; Friedman, C.; Villegas, E.; Jacquemont, C.; Farrugia, D.J.; Couch, F.J.; et al. Secondary mutations as a mechanism of cisplatin resistance in BRCA2-mutated cancers. Nature 2008, 451, 1116–1120. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Edwards, S.L.; Brough, R.; Lord, C.J.; Natrajan, R.; Vatcheva, R.; Levine, D.A.; Boyd, J.; Reis-Filho, J.S.; Ashworth, A. Resistance to therapy caused by intragenic deletion in BRCA2. Nature 2008, 451, 1111–1115. [Google Scholar] [CrossRef] [PubMed]
  48. Tobalina, L.; Armenia, J.; Irving, E.; O’Connor, M.J.; Forment, J.V. A meta-analysis of reversion mutations in BRCA genes identifies signatures of DNA end-joining repair mechanisms driving therapy resistance. Ann. Oncol. 2021, 32, 103–112. [Google Scholar] [CrossRef]
  49. Nelson, A.C.; Holt, J.T. Impact of RING and BRCT domain mutations on BRCA1 protein stability, localization and recruitment to DNA damage. Radiat. Res. 2010, 174, 1–13. [Google Scholar] [CrossRef] [Green Version]
  50. Gogola, E.; Duarte, A.A.; de Ruiter, J.R.; Wiegant, W.W.; Schmid, J.A.; de Bruijn, R.; James, D.I.; Guerrero Llobet, S.; Vis, D.J.; Annunziato, S.; et al. Selective Loss of PARG Restores PARylation and Counteracts PARP Inhibitor-Mediated Synthetic Lethality. Cancer Cell 2018, 33, 1078–1093.e12. [Google Scholar] [CrossRef] [Green Version]
  51. Pilie, P.G.; Gay, C.M.; Byers, L.A.; O’Connor, M.J.; Yap, T.A. PARP Inhibitors: Extending Benefit Beyond BRCA-Mutant Cancers. Clin. Cancer Res. 2019, 25, 3759–3771. [Google Scholar] [CrossRef] [Green Version]
  52. Ame, J.C.; Fouquerel, E.; Gauthier, L.R.; Biard, D.; Boussin, F.D.; Dantzer, F.; de Murcia, G.; Schreiber, V. Radiation-induced mitotic catastrophe in PARG-deficient cells. J. Cell Sci. 2009, 122, 1990–2002. [Google Scholar] [CrossRef] [Green Version]
  53. Kondrashova, O.; Nguyen, M.; Shield-Artin, K.; Tinker, A.V.; Teng, N.N.H.; Harrell, M.I.; Kuiper, M.J.; Ho, G.Y.; Barker, H.; Jasin, M.; et al. Secondary Somatic Mutations Restoring RAD51C and RAD51D Associated with Acquired Resistance to the PARP Inhibitor Rucaparib in High-Grade Ovarian Carcinoma. Cancer Discov. 2017, 7, 984–998. [Google Scholar] [CrossRef] [Green Version]
  54. Roy, R.; Chun, J.; Powell, S.N. BRCA1 and BRCA2: Different roles in a common pathway of genome protection. Nat. Rev. Cancer 2011, 12, 68–78. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Yazinski, S.A.; Comaills, V.; Buisson, R.; Genois, M.M.; Nguyen, H.D.; Ho, C.K.; Todorova Kwan, T.; Morris, R.; Lauffer, S.; Nussenzweig, A.; et al. ATR inhibition disrupts rewired homologous recombination and fork protection pathways in PARP inhibitor-resistant BRCA-deficient cancer cells. Genes Dev. 2017, 31, 318–332. [Google Scholar] [CrossRef] [PubMed]
  56. Bunting, S.F.; Callen, E.; Wong, N.; Chen, H.T.; Polato, F.; Gunn, A.; Bothmer, A.; Feldhahn, N.; Fernandez-Capetillo, O.; Cao, L.; et al. 53BP1 inhibits homologous recombination in Brca1-deficient cells by blocking resection of DNA breaks. Cell 2010, 141, 243–254. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Jaspers, J.E.; Kersbergen, A.; Boon, U.; Sol, W.; van Deemter, L.; Zander, S.A.; Drost, R.; Wientjens, E.; Ji, J.; Aly, A.; et al. Loss of 53BP1 causes PARP inhibitor resistance in Brca1-mutated mouse mammary tumors. Cancer Discov. 2013, 3, 68–81. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  58. Bouwman, P.; Aly, A.; Escandell, J.M.; Pieterse, M.; Bartkova, J.; van der Gulden, H.; Hiddingh, S.; Thanasoula, M.; Kulkarni, A.; Yang, Q.; et al. 53BP1 loss rescues BRCA1 deficiency and is associated with triple-negative and BRCA-mutated breast cancers. Nat. Struct. Mol. Biol. 2010, 17, 688–695. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  59. Xu, G.; Chapman, J.R.; Brandsma, I.; Yuan, J.; Mistrik, M.; Bouwman, P.; Bartkova, J.; Gogola, E.; Warmerdam, D.; Barazas, M.; et al. REV7 counteracts DNA double-strand break resection and affects PARP inhibition. Nature 2015, 521, 541–544. [Google Scholar] [CrossRef] [Green Version]
  60. Liao, H.; Ji, F.; Helleday, T.; Ying, S. Mechanisms for stalled replication fork stabilization: New targets for synthetic lethality strategies in cancer treatments. EMBO Rep. 2018, 19, e46263. [Google Scholar] [CrossRef]
  61. van Wietmarschen, N.; Nussenzweig, A. Mechanism for synthetic lethality in BRCA-deficient cancers: No longer lagging behind. Mol. Cell 2018, 71, 877–878. [Google Scholar] [CrossRef] [Green Version]
  62. Kais, Z.; Rondinelli, B.; Holmes, A.; O’Leary, C.; Kozono, D.; D’Andrea, A.D.; Ceccaldi, R. FANCD2 Maintains Fork Stability in BRCA1/2-Deficient Tumors and Promotes Alternative End-Joining DNA Repair. Cell Rep. 2016, 15, 2488–2499. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  63. Ray Chaudhuri, A.; Callen, E.; Ding, X.; Gogola, E.; Duarte, A.A.; Lee, J.E.; Wong, N.; Lafarga, V.; Calvo, J.A.; Panzarino, N.J.; et al. Replication fork stability confers chemoresistance in BRCA-deficient cells. Nature 2016, 535, 382–387. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  64. Taglialatela, A.; Alvarez, S.; Leuzzi, G.; Sannino, V.; Ranjha, L.; Huang, J.W.; Madubata, C.; Anand, R.; Levy, B.; Rabadan, R.; et al. Restoration of Replication Fork Stability in BRCA1- and BRCA2-Deficient Cells by Inactivation of SNF2-Family Fork Remodelers. Mol. Cell 2017, 68, 414–430.e8. [Google Scholar] [CrossRef] [Green Version]
  65. Dungrawala, H.; Bhat, K.P.; Le Meur, R.; Chazin, W.J.; Ding, X.; Sharan, S.K.; Wessel, S.R.; Sathe, A.A.; Zhao, R.; Cortez, D. RADX Promotes Genome Stability and Modulates Chemosensitivity by Regulating RAD51 at Replication Forks. Mol. Cell 2017, 67, 374–386.e5. [Google Scholar] [CrossRef] [PubMed]
  66. Pettitt, S.J.; Krastev, D.B.; Brandsma, I.; Drean, A.; Song, F.; Aleksandrov, R.; Harrell, M.I.; Menon, M.; Brough, R.; Campbell, J.; et al. Genome-wide and high-density CRISPR-Cas9 screens identify point mutations in PARP1 causing PARP inhibitor resistance. Nat. Commun. 2018, 9, 1849. [Google Scholar] [CrossRef]
  67. Yekezare, M.; Gómez-González, B.; Diffley, J.F. Controlling DNA replication origins in response to DNA damage–inhibit globally, activate locally. J. Cell Sci. 2013, 126, 1297–1306. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  68. Méchali, M. Eukaryotic DNA replication origins: Many choices for appropriate answers. Nat. Rev. Mol. Cell Biol. 2010, 11, 728–738. [Google Scholar] [CrossRef]
  69. Haynes, B.; Murai, J.; Lee, J.M. Restored replication fork stabilization, a mechanism of PARP inhibitor resistance, can be overcome by cell cycle checkpoint inhibition. Cancer Treat. Rev. 2018, 71, 1–7. [Google Scholar] [CrossRef]
  70. Carrassa, L.; Damia, G. DNA damage response inhibitors: Mechanisms and potential applications in cancer therapy. Cancer Treat. Rev. 2017, 60, 139–151. [Google Scholar] [CrossRef]
  71. Jiao, S.; Xia, W.; Yamaguchi, H.; Wei, Y.; Chen, M.K.; Hsu, J.M.; Hsu, J.L.; Yu, W.H.; Du, Y.; Lee, H.H.; et al. PARP Inhibitor Upregulates PD-L1 Expression and Enhances Cancer-Associated Immunosuppression. Clin. Cancer Res. 2017, 23, 3711–3720. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  72. Du, Y.; Yamaguchi, H.; Wei, Y.; Hsu, J.L.; Wang, H.L.; Hsu, Y.H.; Lin, W.C.; Yu, W.H.; Leonard, P.G.; Lee, G.R.t.; et al. Blocking c-Met-mediated PARP1 phosphorylation enhances anti-tumor effects of PARP inhibitors. Nat. Med. 2016, 22, 194–201. [Google Scholar] [CrossRef] [PubMed]
  73. Barkauskaite, E.; Brassington, A.; Tan, E.S.; Warwicker, J.; Dunstan, M.S.; Banos, B.; Lafite, P.; Ahel, M.; Mitchison, T.J.; Ahel, I.; et al. Visualization of poly(ADP-ribose) bound to PARG reveals inherent balance between exo- and endo-glycohydrolase activities. Nat. Commun. 2013, 4, 2164. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  74. Ocaña, A.; Pandiella, A. Proteolysis targeting chimeras (PROTACs) in cancer therapy. J. Exp. Clin. Cancer Res. 2020, 39, 189. [Google Scholar] [CrossRef] [PubMed]
  75. Burslem, G.M.; Crews, C.M. Proteolysis-Targeting Chimeras as Therapeutics and Tools for Biological Discovery. Cell 2020, 181, 102–114. [Google Scholar] [CrossRef] [PubMed]
  76. Alabi, S.B.; Crews, C.M. Major advances in targeted protein degradation: PROTACs, LYTACs, and MADTACs. J. Biol. Chem. 2021, 296, 100647. [Google Scholar] [CrossRef] [PubMed]
  77. Cao, C.; Yang, J.; Chen, Y.; Zhou, P.; Wang, Y.; Du, W.; Zhao, L.; Chen, Y. Discovery of SK-575 as a Highly Potent and Efficacious Proteolysis-Targeting Chimera Degrader of PARP1 for Treating Cancers. J. Med. Chem. 2020, 63, 11012–11033. [Google Scholar] [CrossRef] [PubMed]
  78. Zhang, Z.; Chang, X.; Zhang, C.; Zeng, S.; Liang, M.; Ma, Z.; Wang, Z.; Huang, W.; Shen, Z. Identification of probe-quality degraders for Poly(ADP-ribose) polymerase-1 (PARP-1). J. Enzym. Inhib. Med. Chem. 2020, 35, 1606–1615. [Google Scholar] [CrossRef] [PubMed]
  79. Zhao, Q.; Lan, T.; Su, S.; Rao, Y. Induction of apoptosis in MDA-MB-231 breast cancer cells by a PARP1-targeting PROTAC small molecule. Chem. Commun. 2019, 55, 369–372. [Google Scholar] [CrossRef]
  80. Kim, C.; Chen, C.; Yu, Y. Avoid the trap: Targeting PARP1 beyond human malignancy. Cell Chem. Biol. 2021, 28, 456–462. [Google Scholar] [CrossRef]
  81. Wang, S.; Han, L.; Han, J.; Li, P.; Ding, Q.; Zhang, Q.J.; Liu, Z.P.; Chen, C.; Yu, Y. Uncoupling of PARP1 trapping and inhibition using selective PARP1 degradation. Nat. Chem. Biol. 2019, 15, 1223–1231. [Google Scholar] [CrossRef]
  82. Go, A.; Jang, J.W.; Lee, W.; Ha, J.D.; Kim, H.J.; Nam, H.J. Augmentation of the antitumor effects of PARP inhibitors in triple-negative breast cancer via degradation by hydrophobic tagging modulation. Eur. J. Med. Chem. 2020, 204, 112635. [Google Scholar] [CrossRef] [PubMed]
  83. Szumilak, M.; Wiktorowska-Owczarek, A.; Stanczak, A. Hybrid Drugs-A Strategy for Overcoming Anticancer Drug Resistance? Molecules 2021, 26, 2601. [Google Scholar] [CrossRef] [PubMed]
  84. Wei, L.; Wang, M.; Wang, Q.; Han, Z. Dual targeting, a new strategy for novel PARP inhibitor discovery. Drug Discov. Ther. 2021, 15, 300–309. [Google Scholar] [CrossRef] [PubMed]
  85. Juvekar, A.; Burga, L.N.; Hu, H.; Lunsford, E.P.; Ibrahim, Y.H.; Balmañà, J.; Rajendran, A.; Papa, A.; Spencer, K.; Lyssiotis, C.A. Combining a PI3K Inhibitor with a PARP Inhibitor Provides an Effective Therapy for BRCA1-Related Breast CancerCombination of PI3K-and PARP-Inhibitors to Treat Breast Cancer. Cancer Discov. 2012, 2, 1048–1063. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  86. Wang, J.; Li, H.; He, G.; Chu, Z.; Peng, K.; Ge, Y.; Zhu, Q.; Xu, Y. Discovery of novel dual poly (ADP-ribose) polymerase and phosphoinositide 3-kinase inhibitors as a promising strategy for cancer therapy. J. Med. Chem. 2019, 63, 122–139. [Google Scholar] [CrossRef]
  87. Yin, L.; Liu, Y.; Peng, Y.; Peng, Y.; Yu, X.; Gao, Y.; Yuan, B.; Zhu, Q.; Cao, T.; He, L.; et al. PARP inhibitor veliparib and HDAC inhibitor SAHA synergistically co-target the UHRF1/BRCA1 DNA damage repair complex in prostate cancer cells. J. Exp. Clin. Cancer Res. 2018, 37, 153. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  88. Min, A.; Im, S.A.; Kim, D.K.; Song, S.H.; Kim, H.J.; Lee, K.H.; Kim, T.Y.; Han, S.W.; Oh, D.Y.; Kim, T.Y.; et al. Histone deacetylase inhibitor, suberoylanilide hydroxamic acid (SAHA), enhances anti-tumor effects of the poly (ADP-ribose) polymerase (PARP) inhibitor olaparib in triple-negative breast cancer cells. Breast Cancer Res. 2015, 17, 33. [Google Scholar] [CrossRef] [Green Version]
  89. Yuan, Z.; Chen, S.; Sun, Q.; Wang, N.; Li, D.; Miao, S.; Gao, C.; Chen, Y.; Tan, C.; Jiang, Y. Olaparib hydroxamic acid derivatives as dual PARP and HDAC inhibitors for cancer therapy. Bioorganic Med. Chem. 2017, 25, 4100–4109. [Google Scholar] [CrossRef] [PubMed]
  90. Pommier, Y.; Nussenzweig, A.; Takeda, S.; Austin, C. Human topoisomerases and their roles in genome stability and organization. Nat. Rev. Mol. Cell Biol. 2022, 23, 407–427. [Google Scholar] [CrossRef] [PubMed]
  91. Yuan, Z.; Chen, S.; Chen, C.; Chen, J.; Chen, C.; Dai, Q.; Gao, C.; Jiang, Y. Design, synthesis and biological evaluation of 4-amidobenzimidazole acridine derivatives as dual PARP and Topo inhibitors for cancer therapy. Eur. J. Med. Chem. 2017, 138, 1135–1146. [Google Scholar] [CrossRef]
  92. Stewart, R.A.; Pilie, P.G.; Yap, T.A. Development of PARP and Immune-Checkpoint Inhibitor Combinations. Cancer Res. 2018, 78, 6717–6725. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  93. Ofori, S.; Awuah, S.G. Small-Molecule Poly(ADP-ribose) Polymerase and PD-L1 Inhibitor Conjugates as Dual-Action Anticancer Agents. ACS Omega 2019, 4, 12584–12597. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  94. Thomas, C.; Ji, Y.; Lodhi, N.; Kotova, E.; Pinnola, A.D.; Golovine, K.; Makhov, P.; Pechenkina, K.; Kolenko, V.; Tulin, A.V. Non-NAD-Like poly(ADP-Ribose) Polymerase-1 Inhibitors effectively Eliminate Cancer in vivo. EBioMedicine 2016, 13, 90–98. [Google Scholar] [CrossRef] [Green Version]
Ijms 23 08412 g001 550
Figure 1. Synthetic lethality: mechanism of action of PARP inhibitors. PARPs recognize damaged DNA sites and recruit DNA repairing machineries through PARylation. Failure of repairing single-stranded DNA breaks can lead to DSB, which can be precisely repaired by the homologous recombination (HR) mechanism when the DNA repair system remains intact. However, cells with BRCA1/2 mutations progress to apoptosis. Because BRCA1/2 proteins play a key role in HR, the non-homologous end-joining (NHEJ) pathway is activated instead of HR in case of BRCA1/2 mutated cells. Incorrect repair by NHEJ leads to genomic instability and eventually apoptosis.
Figure 1. Synthetic lethality: mechanism of action of PARP inhibitors. PARPs recognize damaged DNA sites and recruit DNA repairing machineries through PARylation. Failure of repairing single-stranded DNA breaks can lead to DSB, which can be precisely repaired by the homologous recombination (HR) mechanism when the DNA repair system remains intact. However, cells with BRCA1/2 mutations progress to apoptosis. Because BRCA1/2 proteins play a key role in HR, the non-homologous end-joining (NHEJ) pathway is activated instead of HR in case of BRCA1/2 mutated cells. Incorrect repair by NHEJ leads to genomic instability and eventually apoptosis.
Ijms 23 08412 g001
Ijms 23 08412 g002 550
Figure 2. Chemical structures of representative PARP inhibitors.
Figure 2. Chemical structures of representative PARP inhibitors.
Ijms 23 08412 g002
Ijms 23 08412 g003 550
Figure 3. Kaplan–Meier plots for REV7/MAD2L2 mRNA level separation from TCGA and HPA cohorts in pancreatic cancer (A), ovarian cancer (B), and breast cancer (C). The log-rank p values are shown in the lower left corner of each Kaplan–Meier plot. The prognosis of each group of patients was examined by Kaplan-Meier survival estimators, and the survival outcomes of the two groups were compared by log-rank tests. To choose the best fragments per kilobase of exon per million (FPKM) cut-offs for grouping the most significant patients, all FPKM values from the 20th to 80th percentiles were used to group the patients, significant differences in the survival outcomes of the groups were examined, and the value yielding the lowest log-rank p value selected. Genes with log-rank p values less than 0.001 were defined as prognostic genes.
Figure 3. Kaplan–Meier plots for REV7/MAD2L2 mRNA level separation from TCGA and HPA cohorts in pancreatic cancer (A), ovarian cancer (B), and breast cancer (C). The log-rank p values are shown in the lower left corner of each Kaplan–Meier plot. The prognosis of each group of patients was examined by Kaplan-Meier survival estimators, and the survival outcomes of the two groups were compared by log-rank tests. To choose the best fragments per kilobase of exon per million (FPKM) cut-offs for grouping the most significant patients, all FPKM values from the 20th to 80th percentiles were used to group the patients, significant differences in the survival outcomes of the groups were examined, and the value yielding the lowest log-rank p value selected. Genes with log-rank p values less than 0.001 were defined as prognostic genes.
Ijms 23 08412 g003
Ijms 23 08412 g004 550
Figure 4. Restoring fork stabilization can render resistance to PARP inhibitors.
Figure 4. Restoring fork stabilization can render resistance to PARP inhibitors.
Ijms 23 08412 g004
Ijms 23 08412 g005 550
Figure 5. Kaplan–Meier plots for the ZRANB3 in pancreatic cancer (A), HLTF in pancreatic cancer (B), SMARCAL-1 in ovarian cancer (C), PTIP in ovarian cancer (D) or breast cancer (E), and FANCD2 in pancreatic cancer (F) mRNA level separation from the TCGA and HPA cohorts. The log-rank p values are shown in the lower left corner of each Kaplan–Meier plot. The prognosis of each group of patients was examined by Kaplan–Meier survival estimators, and the survival outcomes of the two groups were compared by log-rank tests. To choose the best fragments per kilobase of exon per million (FPKM) cut-offs for grouping the most significant patients, all FPKM values from the 20th to 80th percentiles were used to group the patients, significant differences in the survival outcomes of the groups were examined, and the value yielding the lowest log-rank p value selected. Genes with a log-rank p values less than 0.001 were defined as prognostic genes.
Figure 5. Kaplan–Meier plots for the ZRANB3 in pancreatic cancer (A), HLTF in pancreatic cancer (B), SMARCAL-1 in ovarian cancer (C), PTIP in ovarian cancer (D) or breast cancer (E), and FANCD2 in pancreatic cancer (F) mRNA level separation from the TCGA and HPA cohorts. The log-rank p values are shown in the lower left corner of each Kaplan–Meier plot. The prognosis of each group of patients was examined by Kaplan–Meier survival estimators, and the survival outcomes of the two groups were compared by log-rank tests. To choose the best fragments per kilobase of exon per million (FPKM) cut-offs for grouping the most significant patients, all FPKM values from the 20th to 80th percentiles were used to group the patients, significant differences in the survival outcomes of the groups were examined, and the value yielding the lowest log-rank p value selected. Genes with a log-rank p values less than 0.001 were defined as prognostic genes.
Ijms 23 08412 g005
Ijms 23 08412 g006 550
Figure 6. PARP degradation by proteolysis-targeting chimeras (PROTAC) or hydrophobic-tagged small molecules. Chemical structures used in PARP degradation are shown. Ub, ubiquitin; E3, E3 ligase.
Figure 6. PARP degradation by proteolysis-targeting chimeras (PROTAC) or hydrophobic-tagged small molecules. Chemical structures used in PARP degradation are shown. Ub, ubiquitin; E3, E3 ligase.
Ijms 23 08412 g006
Ijms 23 08412 g007 550
Figure 7. Chemical structures of representative dual inhibitors. Dual inhibitor development for improved outcomes. Concomitant inhibition of PARP and other pathways is achieved by linking two bioactive molecules.
Figure 7. Chemical structures of representative dual inhibitors. Dual inhibitor development for improved outcomes. Concomitant inhibition of PARP and other pathways is achieved by linking two bioactive molecules.
Ijms 23 08412 g007
Table
Table 1. Notable phase 3 and 4 clinical trials that have results.
Table 1. Notable phase 3 and 4 clinical trials that have results.
NCT
Identifier		DrugSetting ConditionsWith ChemoEfficacy (Ref.)
Breast cancer
NCT02163694VeliparibHer2-negative advanced breast cancer; Germline BRCA1/2 mutatedYes; Combination with carboplatin + paclitaxelIncrease in PFS compared with placebo in a germline BRCA1/2 mutation [25,26]
NCT02000622OlaparibHer2-negative metastatic breast cancer patients; Germline BRCA 1/2 mutatedNoBenefit over standard chemotherapy in PFS [20,32]
NCT01945775Talazoparib Advanced or metastatic breast cancer; Germline BRCA mutatedNoBenefit over standard chemotherapy in PFS [29,33]
Approved by U.S. FDA in 2019
NCT01905592NiraparibAdvanced or metastatic breast cancerNoNo significant differences between niparparib and standard chemotherapy in PFS and OS
Ovarian cancer
NCT01847274NiraparibOvarian cancer; platinum-based chemotherapy sensitiveNoIncrease in PFS compared with placebo regardless of the presence or absence of HRD [23,34,35]
NCT02655016Niraparib Advanced ovarian cancer (Stage III or IV); Patients with clinical complete response or partial response following completion of platinum-based chemotherapy course.NoIncrease in PFS compared with placebo regardless of the presence or absence of HDR [36]
Approved by U.S. FDA in 2020 for the maintenance treatment
NCT02470585VeliparibAdvanced ovarian cancer (Stage III or IV); Patients after surgeryYes; Combination with first-line chemotherapyIncrease in PFS compared with placebo regardless of the presence or absence of HRD [27]
NCT01968213RucaparibOvarian, fallopian, peritoneal cancer; Patients with clinical complete response or partial response following completion of platinum-based chemotherapy course.NoIncrease in PFS, CFI, TFST, TSST, and PSF2 compared with placebo in recurrent ovarian cancer regardless of the presence or absence of HDR [37,38,39]
Approved by U.S. FDA in 2018 for the maintenance treatment
NCT01874353OlaparibRelapsed high grade serous ovarian cancer; platinum-based chemotherapy sensitive; BRCA1/2 mutatedNoIncrease in PFS and OS compared with placebo [40,41,42,43]
Approved by U.S. FDA in 2017 for the maintenance treatment
NCT01844986OlaparibAdvanced Ovarian Cancer (Stage III, IV); BRCA1/2 mutated; Patients with clinical complete response or partial response following completion of platinum-based chemotherapy course.NoIncrease in PFS compared with placebo regardless of the presence or absence of HRD [44,45]
Lung cancer
NCT02106546VeliparibAdvanced or metastatic squamous non-small cell lung cancer (NSCLC); Yes; Combination with carboplatin + paclitaxelFavorable OS in the 52-gene expression histology classifier (LP52)-positive population by veliparib; Favorable OS in the LP52-negative population by placebo [28]
Pancreatic cancer
NCT02184195OlaparibMetastatic pancreatic cancer; Germline BRCA1/2 mutated; No progression during first-line platinum-based chemotherapy No Increase in PFS compared to placebo with a germline BRCA1/2 mutation [21]
Approved by U.S. FDA in 2019 for the maintenance treatment
Table
Table 2. PROTAC or hydrophobic-tagged PARP inhibitors.
Table 2. PROTAC or hydrophobic-tagged PARP inhibitors.
PROTAC
PARP BinderE3 Ligase BinderTested CellNoteRef.
OlaparibCRBN ligandMDA-MB-436 (BRCA1 mutated breast cancer cells), Capan-1 (BRCA2 mutated pancreatic cancer cells), SW620 (colon cancer cell)Inhibition of tumor growth, Xenograft assay[77]
RucaparibCRBN ligandPrimary rat neonatal cardiomyocytes, C2C12 (myoblast)PARP1 non-trapping, No genotoxic induced cell death[81]
OlaparibCRBN ligandSW620Increased apoptosis[78]
NiraparibMDM2 ligandMDA-MB-231 (TNBC)Induction of PARP1 cleavage, increased apoptosis[79]
Hydrophobic Tagging
PARP BinderHydrophobic MoietyTested CellNoteRef.
OlaparibFluoreneMDA-MB-231, MDA-MB-468 (TNBC),
HCC1937 (BRCA1 mutated breast cancer cells)		Increased apoptosis and ER stress[82]
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Kim, D.; Nam, H.J. PARP Inhibitors: Clinical Limitations and Recent Attempts to Overcome Them. Int. J. Mol. Sci. 2022, 23, 8412. https://doi.org/10.3390/ijms23158412

AMA Style

Kim D, Nam HJ. PARP Inhibitors: Clinical Limitations and Recent Attempts to Overcome Them. International Journal of Molecular Sciences. 2022; 23(15):8412. https://doi.org/10.3390/ijms23158412

Chicago/Turabian Style

Kim, Dongha, and Hye Jin Nam. 2022. "PARP Inhibitors: Clinical Limitations and Recent Attempts to Overcome Them" International Journal of Molecular Sciences 23, no. 15: 8412. https://doi.org/10.3390/ijms23158412

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop