Signaling Pathways and Natural Compounds in Triple-Negative Breast Cancer Cell Line

Triple-negative breast cancer (TNBC) is the most aggressive subtype of breast cancer, having a poor prognosis and rapid metastases. TNBC is characterized by the absence of estrogen, progesterone, and human epidermal growth receptor-2 (HER2) expressions and has a five-year survival rate. Compared to other breast cancer subtypes, TNBC patients only respond to conventional chemotherapies, and even then, with limited success. Shortages of chemotherapeutic medication can lead to resistance, pressured index therapy, non-selectivity, and severe adverse effects. Finding targeted treatments for TNBC is difficult owing to the various features of cancer. Hence, identifying the most effective molecular targets in TNBC pathogenesis is essential for predicting response to targeted therapies and preventing TNBC cell metastases. Nowadays, natural compounds have gained attention as TNBC treatments, and have offered new strategies for solving drug resistance. Here, we report a systematic review using the database from Pubmed, Science Direct, MDPI, BioScince, Springer, and Nature for articles screening from 2003 to 2022. This review analyzes relevant signaling pathways and the prospect of utilizing natural compounds as a therapeutic agent to improve TNBC treatments in the future.


Introduction
According to the Globocan Database of the International Agency for Research on Cancer (IARC), breast cancer had the highest incidence in 2018. Breast cancer mortality rates in Indonesia were about 16.7%, or 58.256 million, while morbidity rates were around 11%, or 22.692 million. The majority of triple-negative breast cancer (TNBC) patients are young women with a BRCA1 gene mutation [1]. TNBC is characterized by the absence of estrogen, progesterone, and HER2 receptor expression [2]. It comprises about 15-20% of all breast cancer cases [3].
The major cause of mortality in TNBC patients is metastasis [4] to distant areas such as the bone, lung, and brain, rather than the tumor of breast cancer [5,6]. The metastatic migration or spread of breast cancer from primary tumors to other cell components is initiated by intravasation, survival, extravasation in circulation, and colonization [7]. Tumor cell instability can also potentially induce metastasis, allowing these cells to spread to other

Triple-Negative Breast Cancer
Triple-negative breast cancer (TNBC), accounts for about 10-15% of all breast can cases, and this is due to the lack of immunohistological expression of progesterone rec tor (PR), estrogen receptor (ER), and human epidermal growth factor receptor 2 (HE This disease is characterized as a malignant tumor that is invasive and susceptible to first metastasis [11]. TNBC has been associated with differential breast cancer, whic still difficult to characterize in the molecular phase due to the lack of a definitive progn tic marker and specific targeted therapy. Moreover, TNBC is indicated as a type of br cancer that has an aggressive clinical behavior, a high rate of proliferation, and a p prognosis, as well as a mutation in the breast cancer gene 1 (BRCA1) [37][38][39]. The BL-1 subtype has the highest prevalence of TP53 gene mutations, which aff gene expression, cell cycle, DNA damage response, and regulation. In contrast, the B subtype was associated with high gene expression of the growth factor pathway and m abolic pathway activity. The IM subtype is related to the immune cell pathway, high tigen, and cytokine signaling expression including TNF, NF-κB, and JAK/STAT pathw The mesenchymal and MSL subtypes are responsible for gene expression to cell moti cellular differentiation, and epithelial-mesenchymal transition (EMT) in the MSL of a ogenesis-enriched genes, while the LAR subtype is enriched for androgen receptor pression and has higher mutation genes in PI3KCA, AKT1, and CDH1. The intrinsic ba like subtype was seen in many BL-1 and BL-2 cancers associated with BRCA mutati

Triple-Negative Breast Cancer
Triple-negative breast cancer (TNBC), accounts for about 10-15% of all breast cancer cases, and this is due to the lack of immunohistological expression of progesterone receptor (PR), estrogen receptor (ER), and human epidermal growth factor receptor 2 (HER2). This disease is characterized as a malignant tumor that is invasive and susceptible to the first metastasis [11]. TNBC has been associated with differential breast cancer, which is still difficult to characterize in the molecular phase due to the lack of a definitive prognostic marker and specific targeted therapy. Moreover, TNBC is indicated as a type of breast cancer that has an aggressive clinical behavior, a high rate of proliferation, and a poor prognosis, as well as a mutation in the breast cancer gene 1 (BRCA1) [37][38][39].
The BL-1 subtype has the highest prevalence of TP53 gene mutations, which affects gene expression, cell cycle, DNA damage response, and regulation. In contrast, the BL-2 subtype was associated with high gene expression of the growth factor pathway and metabolic pathway activity. The IM subtype is related to the immune cell pathway, high antigen, and cytokine signaling expression including TNF, NF-κB, and JAK/STAT pathways. The mesenchymal and MSL subtypes are responsible for gene expression to cell motility, cellular differentiation, and epithelial-mesenchymal transition (EMT) in the MSL of angiogenesis-enriched genes, while the LAR subtype is enriched for androgen receptor expression and has higher mutation genes in PI3KCA, AKT1, and CDH1. The intrinsic basal-like subtype was seen in many BL-1 and BL-2 cancers associated with BRCA mutations [40]. The molecular classification of TNBC and ongoing clinical potential therapies in vitro is shown in Table 1. Table 1. Molecular classification of triple-negative breast cancer and ongoing clinical potential therapies in vitro adapted with permission from   [41] and Ahn et al. 2016 [14]. --Abbreviations: Cytotoxic T lymphocyte-associated protein 4 (CTLA-4); epithelial-mesenchymal transition (EMT); epidermal growth factor receptor (EGFR); fibroblast growth factor receptor (FGFR); histone deacetylase (HDAC); human epidermal growth factor receptor 2 (HER2); Janus kinase (JAK); lymphocyte-activation gene 3 (LAG-3); mechanistic target of rapamycin (mTOR); programmed cell death protein 1 (PD-1); programmed death-ligand (PD-L1); poly-ADP ribose polymerase (PARP); phosphoinositide 3-kinase (PI3K); T-cell immunoglobulin and mucin-domain containing-3 (TIM-3); trophoblast antigen 2 (Trop-2); vascular endothelial growth factor receptor (VEGFR).
Six TNBC molecular clusters were identified by two in silico studies. Basal-like 1, basal-like 2, immunomodulatory, mesenchymal, mesenchymal stem-like, and luminal androgen receptors were discovered in the first study, while immunity 1, immunity 2, pro- liferation/DNA damage, androgen receptor-like, matrix/invasion 1, and matrix/invasion 2 were described in the subsequent study [48].

Targeted Therapy of Triple-Negative Breast Cancer
Various efforts have been carried out to examine the problems in TNBC treatment. Chemotherapy, such as anthracyclines, ixabepilone, taxanes, and platinum drugs, is the most common treatment for TNBC patients [49]. However, not all chemotherapy patients had beneficial results, and it is still unclear whether the treatment is based on their TNBC subtypes. Efforts in developing therapies for target-specific TNBC biomarkers and TNBC therapy are ongoing [50]. These strategies, which include EGFR-targeted agents, androgen receptor-targeted agents, anti-antigenic agents, PARP inhibitors, immune-targeted, and Wnt/β-catenin signaling pathways, provide options for the triple-negative disease. However, their use in clinical trials is limited, and more research is needed to identify targets with high therapeutic ratios [51]. The mechanism of targeted therapies in TNBC is shown in Figure 2.
Six TNBC molecular clusters were identified by two in silico studies. Basal-like 1, basal-like 2, immunomodulatory, mesenchymal, mesenchymal stem-like, and luminal androgen receptors were discovered in the first study, while immunity 1, immunity 2, proliferation/DNA damage, androgen receptor-like, matrix/invasion 1, and matrix/invasion 2 were described in the subsequent study [48].

Targeted Therapy of Triple-Negative Breast Cancer
Various efforts have been carried out to examine the problems in TNBC treatment. Chemotherapy, such as anthracyclines, ixabepilone, taxanes, and platinum drugs, is the most common treatment for TNBC patients [49]. However, not all chemotherapy patients had beneficial results, and it is still unclear whether the treatment is based on their TNBC subtypes. Efforts in developing therapies for target-specific TNBC biomarkers and TNBC therapy are ongoing [50]. These strategies, which include EGFR-targeted agents, androgen receptor-targeted agents, anti-antigenic agents, PARP inhibitors, immune-targeted, and Wnt/β-catenin signaling pathways, provide options for the triple-negative disease. However, their use in clinical trials is limited, and more research is needed to identify targets with high therapeutic ratios [51]. The mechanism of targeted therapies in TNBC is shown in Figure 2.  The progress of immunotherapy in breast cancer is related to the biological nature of breast cancer and the immune system. Cancer is caused by a variety of processes that avoid the reaction of the immune system. Activated T-cells, pro-B cells, natural killer cells, dendritic cells, and monocytes all express the PD-1 antigen [52]. PD-1 and its ligands, PD-L1 and PD-L2, have a significant role in maintaining T-cell tolerance [52,53]. PD-1 and PD-L1 are explicitly expressed in basal-like breast cancer [53].
Cytotoxic T Lymphocyte-Associated Protein 4 (CTLA-4) CTLA-4 is a type 1 receptor expressed in lymphocytes and T-cells with an IgV-like domain. When CTLA-4 is activated, it is found in intracellular vesicles and is quickly exported to the cell surface, resulting in efficient regulatory T-cell (Treg) suppression [52]. CTLA-4 is one of the immune checkpoint proteins expressed on activated T-cells [54]. The current study has led researchers to believe that utilizing Tregs as an anti-CTLA-4 therapy is one of the most critical factors for therapeutic responses [55,56].
CD28 is a protein constructor for CTLA-4. Both ligands, CD80 and CD86, are identical, but CTL-4 has a greater affinity. CD28 and CTLA-4 also have the same intracellular bonding pairs, the tp85 subunit of PI3K and PPA2 phosphatase. CTLA-4 is also expressed on regulatory T-cells mediating immunosuppressive responses. CTLA-4 suppresses T-cells by binding to CD80 and CD86, preventing CD28 stimulation and inhibiting T-cell activation. Another way is through CTLA-4 depleting B7 protein in APC, preventing B7 from performing its critical function of suppressing immunological responses in the body [57]. Ipilimumab is a checkpoint blocker and an anti-CTLA-4 monoclonal antibody that is presently being tested in clinical trials in combination with nivolumab or the combination of nivolumab and INCAGN01876 (anti-human glucocorticoid-induced tumor necrosis factor [TNF] receptor). Tremelimumab, an anti-CTLA-4 monoclonal antibody, is being tested in combination with PF-06936308, nab-paclitaxel, Carboplatin, and durvalumab in clinical trials.

Lymphocyte Activation Gene 3 (LAG-3)
LAG-3 is a type 1 transmembrane protein with CD4-like properties. LAG-3 has an immune system suppressive effect, although the exact mechanism is uncertain. As previously mentioned, LAG-3 has a larger extracellular domain than other immune checkpoint molecules, and its intracellular mechanisms are unique from those of other immune checkpoints. Expressions of LAG-3 have been detected in activated T cells, B cells, NK cells, and plasmacytoid dendritic cells. LAG-3 binds to MHC II receptors with a higher affinity level. Antigen-presenting cells are amplified with a competitive inhibitor on LAG-3/MHC II receptor binding. When combined with paclitaxel, IMP321 (LAG-3Ig) had an objective response rate of 50% as the first-line therapy for TNBC [58].

T Cell Immunoglobulin and Mucin-Domain Containing-3 (TIM-3)
TIM-3 is a member of the TIM protein family and an immunological checkpoint that works in conjunction with PD-1 and LAG-3 to weaken CD8+ T cells. Immune cells including monocytes and macrophages, dendritic cells, mast cells, and natural killer cells all express TIM-3. In addition, TIM-3 mediates the stimulation of the T-cel-CD8 response. INCAGN02390, an anti-TIM-3 antibody, is currently undergoing phase I clinical trials in a variety of advanced malignancies, including TNBC [59].

Hedgehog (Hh) Signaling Pathway
The Hh signaling pathway is involved in angiogenesis, embryogenesis, and cell fate regulation. This signaling pathway regulates the immune system and has been linked to TNBC growth and cancer cell stemness. In TNBC relationships with low overall survival, the hedgehog ligand has a noble expression.
TNBC cells grow, invade, and migrate more quickly when the Hh pathway is activated [31,60]. Three glioma-associated oncogenes (GLI) transcription factors, GLI1, GLI2, and GLI3, are effectors of Hh signaling that regulate the expression of pathway target genes [61]. TNBC has higher basal expression levels of the Hh signaling pathway gene such as GLI1 and GLI2, which are downstream of Hh ligands, than other breast cancers [31].
According to preclinical research, the Hh pathway plays a key role in the maintenance of the cancer stem cell phenotype, activation of cancer-associated fibroblasts, invasive behavior, and angiogenesis in TNBC. The activation mechanism is mostly non-canonical, including direct transcriptional upregulation of GLI1 and GLI2. The United States Food and Drug Administration (FDA) has approved two Hh signaling inhibitors, Vismodegib (NCT02694224) and sonidegib (NCT02027376), for clinical studies in TNBC patients.
Extrinsic regulation was obtained by upregulating GLI1 transcription in Hh signaling pathway activation, such as the PI3K-Akt-mTOR pathway [62], K-Ras, c-Myc, Wnt-beta catenin, and TGFβ [31,63,64]. Deviating transcriptional upregulation of GLI1 is seen downstream of NF-κB in claudin-low breast cancer, a sub-type of TNBC [65]. Furthermore, NF-B induced the transcription factor Forkhead Box C1 (FOXC1), which is an upstream mediator of Hh signaling via upregulation of GLI2 expression in basal-like breast cancer cells. In TNBC cell lines, inhibitors of the Hh pathway, such as GANT61 and Thiostrepton, were shown to inhibit stem cell phenotypes including CD44+/CD24ve cells and sphereforming capacity [31].

Target Deep the Nucleus
Breast Cancer Susceptibility Gene (BRCA) and Platinum-Based Treatment BRCA1 and BRCA2 are two different tumor suppressor genes that play a role in responding to cellular stress by activating the double-stranded DNA repair process. The result inferred that mutations in these two genes cause DNA instability, making cells more susceptible to DNA-destroying agents such as Cisplatin and its derivative, Carboplatin [66], and PARP inhibitors. In addition, most BRCA mutations are associated with hereditary breast cancer, which is the most well-known cause of hereditary cancer predisposition [67,68].
The lifetime risk of breast cancer in carriers of BRCA1 and BRCA2 mutations is 45-80%. Characterized TNBC is more aggressive and has a higher tumor rate. About 80% of tumors have BRCA1 mutations. Despite the risk of a more aggressive tumor phenotype, most investigations have failed to show that BRCA mutation carriers have different clinical outcomes [69]. The cumulative risk of developing breast cancer at the age of 70 for carriers of BRCA mutations is 65% for BRCA1 and 45% for BRCA2. BRCA2-related breast tumors are dominantly ER-positive and p53 negative, while BRCA1-related breast tumors are more often in triple-negative breast cancer (TNBC) and p53 positive [70].
Platinum agents, such as anthracyclin and antimetabolite, are administered in the same metastatic setting and adjuvant as other conventional chemotherapy. In phase II clinical trials, platinum agent monotherapy was found to be effective in patients with BRCA1/2 mutations [66]. Furthermore, the advantage of Cisplatin in conjunction with Gemcitabine is applicable [68]. A clinical study using PARP inhibitors, such as Olaparib and BSI-201, is now ongoing and shows clinical efficacy in the treatment of BRCA1/2-related breast, ovarian, and prostate cancers, as well as sporadic basal-like breast cancers [71].

Poly-ADP Ribose-Polymerases (PARP)
The poly ADP-ribose polymerase (PARP) enzymes repairs DNA damage for maintaining BRCA-mutated cell viability in healthy cells and cancer. Several studies have reported that drugs that interfere with or inhibit the PARP enzyme make it more difficult for cancer cells with BRCA1/2 mutations to repair DNA damage. Cancer cells get a higher chance of survival as a response to this. On the other hand, PARP inhibitors make certain cancer cells less likely to survive DNA damage [72,73].
Clinical trials evaluating the oral PARP inhibitor olaparib in BRCA1/2-positive metastatic breast cancer are currently underway, with interim results showing efficacy [74]. Veliparib is another PARP inhibitor presently being assessed for metastatic TNBC combined with paclitaxel and Carboplatin [75]. Lynparza (Olaparib) and Talzenna (Talazoparib) have been PARP inhibitors that were approved to treat advanced HER2-negative breast cancer in people with BRCA1/2 mutations. Additionally, Atezolizumab, combined with Abraxane chemotherapy drug (chemical name: albumin-bound paclitaxel or nab-paclitaxel), is approved as the first treatment for advanced three-negative or metastatic local metastatic non-resection [73,75].

Histone Deacetylase (HDAC)
Histone acetyltransferases (HATs) catalyze the reversible process of lysine acetylation at the ε-amino group of proteinogenic lysine residues. Histone acetylation neutralizes the positive charge of lysine residues, correlated to chromatin relaxation and active gene transcription [76]. Besides, histone deacetylases (HDACs), which are functional antagonists of HATs, remove the acetyl groups [77], thus leading to a compressed chromatin structure (heterochromatin) and subsequently suppressing gene transcription [78]. TNBC agents that inhibit histone deacetylase (HDAC) play an important role in gene expression, cell proliferation, and survival [79,80].
Currently, Entinostat is an HDAC inhibitor that has been proven to have anti-CSC activity in TNBC stem cells. Entinostat treatment reportedly inhibited TNBC stem cell, tumor growth, and miR-181a expression in TNBC cell lines, as well as inhibiting lung metastases in an in vivo study [81]. Furthermore, in vivo and in vitro studies showed that combining entinostat, retinoic acid, and doxorubicin induced apoptosis and differentiation of TNBC stem cells [82].
An in vivo study showed that Panobinostat (LBH589) decreased cell survival and cell cycle development at the G2/M stage in TNBC cell lines. It also increased the acetylation of the histones H3 (Lys3) and H4 (Lys8) [79]. The drug panobinostat reversed the M phenotype in invasive breast carcinoma via inducing and upregulating cadherin-1 (CDH1) as a Wnt signaling component. In an in vivo investigation, the combination of salinomycin with panobinostat significantly inhibited the growth of TNBC stem cells in TNBC patient-derived xenografts. It inhibited cell cycle progression, regulated EMT, and increased apoptosis in TNBC stem cells in a synergistic manner [83]. p53 p53 is a known oncogene, the tumor suppressor gene. It is responsible for DNA damage repair, as well as apoptosis in cases of no replacement DNA damage or influencing, cell cycle arrest, necrosis, or autophagy. Mutations in p53, usually in TNBC, are approximately 60-70% [16].

Targeting of Intracellular and Signaling Pathways Androgen Receptor
Androgen receptors (AR) are hormonal steroid receptors that include nuclear receptor families and estrogen, glucocorticoid, mineralocorticoid receptors, and transcription factors. Characteristic of the androgen receptor, having overexpression involves a subtype of TNBC [84,85]. It links a transcription factor that controls specific genes, stimulates or suppresses cell proliferation and apoptosis, and activates signaling pathways [14,86,87]. Androgen receptor overexpression can be seen in 70-90% of breast cancers, with 10-50% of TNBC resulting from that expression [88,89].
Research on the relationship between AR and decreased relapse-free survival [90], higher mortality rate [91], or making survival benefit [92,93] are controversial. However, this class of TNBC has become a promising target for anti-androgen therapy.
Bicalutamide is an AR inhibitor used in phase II trial studies in metastatic breast cancer patients [94]. Enzalutamide is an inhibitor of AR nuclear localization that has been well-tolerated in phase II clinical trials, with a CBR of 35% at 16 weeks and a median PFS of 14% [89,95,96]. In a phase II trial, seviteronel (INO-464), an oral selective cytochrome P450c17a (CYP17), 17,20-lyase (lyase), and androgen receptor (AR) inhibitor, showed promising antitumor activity in TNBC patients [97].

Heat Shock Protein 90 (HSP90)
Hsp90 expression levels were found in all subtypes of breast cancer receptors [98]. TNBC was sensitive to Hsp90 inhibition in preclinical and in vitro studies due to the downregulation of the Ras/Raf/MARK pathway [99]. Hsp90 interacts with estrogen receptors (ER), angiogenesis transcription factor HIF-1alpha, tumor suppressor p53 protein, antiapoptotic kinase Akt, Raf-1-MAP kinase, and a family of receptor tyrosine kinases including HER2 [100].
The HSP90 inhibitor (17-DMAG) is more sensitive in the LAR class of TNBC cell lines than basal-like or mesenchymal cell lines [101]. In a phase II clinical trial, single-agent ganetespib was shown to have good tolerability and be able to decrease lung tumor metastases in TNBC patients [102]. Since the clinical study of the combination of onalespib and talazoparib (PARPi) has been withdrawn, the clinical study was conducted using a combination of onalespib and paclitaxel instead [54]. According to in vivo and in vitro experiments, simvastatin acts as an Hsp90 inhibitor in TNBC cells by inhibiting the development of the K292acetylated Hsp90/Cdc37 complex. Simvastatin with Panobinostat (LBH589) is a deacetylase inhibitor based on hydroxamic acid that targets TNBC specifically [103].

Cyclin-Dependent Kinases (CDKs)
CDKs are the only cell cycle and factor transcriptional regulators. Overexpression of CDKs, such as CDK4 and CDK6, is a common characteristic of many cancers, including TNBC. Most of the inhibitors of CDKs have exhibited anti-TNBC activity in vivo and in vitro. Dinaciclib was shown to be a pan-CDK inhibitor in a phase I clinical trial, with no toxicity issues in combination with epirubicin (dinaciclib 20 mg/m 2 on day one and epirubicin 75 mg/m 2 on day 2 of a 3-week cycle) in 9 TNBC patients [104]. The Dinaciclib combination with pembrolizumab is being studied in phase I and phase II clinical trials with a dose of 33 mg/m 2 on cyclin D1 in 8 days from a 21-day cycle [105]. However, phase II clinical studies are now investigating Trilaciclib; a CDK4/6 inhibitor, ribociclib; a CDK6 inhibitor, cyclin D1/CDK4, and PF-06873600, abemaciclib, CDK2/4 inhibitors.

RAF-MEK-ERK Pathway
The higher expression of various genes in the Raf/MEK/ERK pathway and AKT/MEK pathway [110] was involved in the TNBC subtype. It is important to target this signaling pathway in TNBC. Trametinib, a MEK1/2 inhibitor, showed more upregulation and activation of receptor tyrosine kinase [111]. A clinical trial in 50 TNBC patients found that either a single medication or a combination of drugs with an AKT inhibitor (GSK2141795) had low effectiveness. Trametinib, in conjunction with spartalizumab (anti-PD1), was the subject of another clinical trial [112]. Another MEK inhibitor, in combination with BKM120 and BEZ235, completed a clinical trial, but the findings were not published.
The Janus kinase 2 (JAK-2) gene was located on chromosome 9p24.1. Its protein is a tyrosine kinase by the JAK-STAT pathway, which shows that TNBC tumors are related to a poorer prognosis and shorter survival [115,116], and amplified JAK2 are more sensitive to the effects of specific inhibitors in TNBC cells [114].
Cell proliferation in the mammary gland develops during puberty and pregnancy, and cancer is all mediated by the JAK-STAT pathway. Ruxolitinib is a tyrosine kinase inhibitor that targets JAK1 and JAK2. This drug would affect the importance of JAK2 in TNBC.
These include combination with pembrolizumab in advanced TNBC patients, paclitaxel, doxorubicin or cyclophosphamide, and paclitaxel to treat triple-negative inflammatory breast cancer. Ruxolitinib did not meet the primary efficacy target as a single agent in this refractory patient population, despite the evidence of on-target activity [117].
Signal Transducer and Activator of Transcription 3 (STAT-3) STAT3 was discovered binding to DNA in response to interleukin-6 (IL-6) and epidermal growth factor (EGF) during inflammation [118,119]. Overexpressed signal transducer and activator of transcription 3 (STAT3) are highly associated with cancer initiation, metastasis, cell survival, cell cycle progression [66,119], proliferation, migration, invasion, anti-apoptosis, angiogenesis, chemoresistance, immunosuppression, and stem cell self-renewal and differentiation of TNBC cells of clinical and preclinical studies [120,121]. STAT3 inhibitors have since been shown to be effective in inhibiting TNBC tumor growth and metastasis in clinical trials.
Currently, STAT3 small molecule inhibitors and targeting strategies have shown anticancer activity in TNBC in vivo and in vitro [120,122]. STAT3 minor molecule inhibitors, which are more selective and efficacious, are critical for TNBC prevention and therapy [123].
TTI-101 and OPB-51602 are small molecules that inhibit STAT3 activation via inhibiting JAK-mediated tyrosine phosphorylation. These molecules connect to the phosphotyrosine peptide binding site inside of the Src homology 2 molecules (SH2). A phase I study of TTI-101 and OPB-51602 is currently recruiting breast cancer patients. The STAT3 inhibitor AZD9150 is used to treat patients with advanced solid tumors in phase I and II clinical studies, either alone or in combination with chemotherapy [124].
Wnt/β-Catenin Signaling Pathway TNBC can be expressed by Wnt signaling. Wnt signaling acts as a complex antagonist of β-catenin destruction to affect cancer cells and metastases and control the immune system. Research by De et al. (2016) shows that TNBC cells migrate and become invasive clonogenic through upregulation of the Wnt/β-catenin pathway. Wnt/β-catenin plays an essential role as a regulator adhesion cell. The research was focused on the role of β-catenin as a therapeutic agent in TNBC.
The canonical Wnt pathway is a transcription coactivator on TCF/LEF that induces the accumulation of β-Catenin protein and its translocation from the cytoplasm into the nucleus, stimulating the expression of numerous genes involved in cell proliferation, cell migration, and so on. The study shows that increasing regulation and maintaining Wnt/β-Catenin signaling in TNBC is associated with metastasis and poor prognosis.
LGK-974, a Porcupine inhibitor, is a small molecule that inhibits the Wnt signaling pathway in vitro and in vivo by decreasing LRP6 phosphorylation and Axin2 expression.
A single drug has been tested in phase I clinical studies in people with TNBC [125]. In vitro studies have revealed that combining LGK-974 with a PI3K/Akt/mTOR inhibitor reduces cell viability and enhances anti-cancer efficacy in TNBC cell lines [126,127].
In vitro and in vivo studies demonstrate that CWP232228 inhibits the stem cell growth in TNBC cell lines by antagonizing the binding of β-catenin to T-cell factor (TCF) in the nucleus, which is required for breast cancer metastasis and recurrence [128]. PRI-724 is a CRB protein inhibitor [125]. OMP-18R5 (Vantictumab) is a monoclonal antibody that binds to Frizzled7 in the extracellular domain and suppresses the development of human tumors in a xenograft model while having a synergistic effect with chemotherapeutic agents [129]. OTSA101 is an inhibitor of frizzled10, and OMP-54F28 (Ipafricept) is a fusion protein cysteine-rich domain of frizzled-8 receptors with the immunoglobulin for competition in ligands as antagonist Wnt signaling [130,131].

Targeting of Cell Surface Vascular Endothelial Growth Factor Receptor 2 (VEGFR2)
The vascular endothelial growth factor receptor (VEGFR2) is a receptor tyrosine kinase that regulates angiogenesis and pathogenesis in breast cancer [132]. VEGF, the ligand to VEGFR2, impacts ligand expression involving tumor invasion and metastasis in TNBC [133][134][135][136]. Patients who have had TNBC surgery have significantly higher levels of VEGF and shorter survival [137].
VEGFR inhibitors, such as bevacizumab, ramucirumab, VEGFR receptor blockers, receptor mimetics (such as aflibercept), and sorafenib, are small-molecule tyrosine kinase inhibitors [134]. Patients with TNBC who were treated with the medication of sunitinib for metastasis alone had a worse prognosis than those in a phase II trial [133].

Epidermal Growth Factor Receptor (EGFR)
The epidermal growth factor receptor (EGFR) is an HER family tyrosine kinase receptor that is found in a variety of epithelial tumors [138]. EGFR activation has an essential function in the survival of many solid tumors, including metastasis, cell proliferation, invasion, cell cycle progression, differentiation, angiogenesis, and apoptosis. Overexpression EGFR in breast cancer cells is approximately 15-45% [139], and about 50% in TNBC [140], which is negatively correlated with patient survival rates [141]. Anti-EGFR monoclonal antibodies such as cetuximab (SCT200), and EGFR small-molecule tyrosine kinase inhibitors such as gefitinib and erlotinib, are used to block the EGFR signaling pathway in TNBC [138]. Afatinib has been included in clinical studies, however, its status is still unclear. In a phase II trial, erlotinib, in combination with paclitaxel nanoparticle formulation and bevacizumab, showed excellent tolerability [142].

Fibroblast Growth Factor Receptor (FGFR)
FGFR2 is overexpressed in TNBC cells by around 4%, while FGFR1 and FGFR2 mutations were found in roughly 16% and 13% of TNBC patients, respectively [143]. The expression of FGFR2 in TNBC patients is an independent prognostic factor. Approximately 4% of TNBC have amplification of the FGFR2 gene on chromosome 10q26. Nevertheless, it appears to be a rare occurrence in other tumor subtypes, with just 1-2% of all breast cancers expressing it [144,145]. IM-412 is a small molecule tyrosine kinase inhibitor or monoclonal antibody in the TNBC subtype [146].

Trophoblast Antigen 2 (Trop-2) Inhibitor
Trop-2 is a cell surface receptor and an epithelial glycoprotein-1. Overexpression of Trop-2 can promote cancer cell proliferation, EMT, migration, invasion, and metastasis in a variety of epithelial malignancies. For example, Trop-2 was discovered in TNBC cells, with more than 85% of its expression in tumors [147,148].

Glycoprotein Non-Metastatic B (GPNMB)
GPNMB is a type I transmembrane glycoprotein that is overexpressed in 40-60% of breast cancer cases, including triple-negative cases [151]. In phase I/II trials, glembatumumabvedotin (CDX-101), an antibody targeting GPNMB, exhibited a favorable safety profile on 42 patients with metastatic breast cancer [152,153]. However, the results of a further phase II clinical trial in TNBC patients with metastatic CDX-011 impact have yet to be reported.

Natural Compounds for TNBC Treatments
Natural compounds have the potential to be used as therapeutic agents in the treatment of TNBC. Some natural compounds and potential molecular targets in the TNBC signaling pathway have been identified as an anti-cancer treatment. It has recently been shown that determining the concentration or dose of biological substances with comparable chemical components and effects, particularly for various anti-cancer treatment medicines, does not necessarily result in the same anti-cancer effectiveness [154]. As a result, the concentration/dose of natural components in anti-cancer treatment should be considered.
Many natural substances with anti-cancer activities have gotten a lot of attention due to their various behaviors. The conventional treatment approach to breast cancer appears to be limited by several problems. The most critical problem is the toxic effects of treatment resistance. As a result, these numerous cancer treatments have been developed, many of which involve natural compounds such as vinca alkaloids, taxanes, podophyllotoxins, and anthracyclines (doxorubicin) [155]. Plant-derived compounds have a promising synergistic relationship with a variety of chemotherapy regimens, enhancing their effectiveness. Genistein and doxorubicin have a synergistic effect and boost the tamoxifen effect, and pomegranate, which promotes the tamoxifen-induced cell viability inhibition, are two examples of these combinations. Natural materials are also preferred over conventional therapies since they are easily accessible in the natural environment and typically have fewer side effects on healthy human cells.

Luteolin
Luteolin is a flavonoid compound found in many plants such as carrots, celery, broccoli, perilla leaf, and seed [159]. A study that used two methods to determine the mechanisms of luteolin on TNBC metastasis (in vitro with a xenograft model and in vivo with MDA-MB-231 and BT5-49 cell lines), found that Luteolin dose-dependently inhibited cell migration and invasion, reversed epithelial-mesenchymal transition (EMT), and suppressed the expression of β-catenin mRNA that then suppressed metastases to the lung of breast cancer cells at a concentration of 100 µM. The result indicated that luteolin had a potent therapeutic effect on invasion and metastasis of TNBC, which may be involved in the reversal of EMT by down-regulation of β-catenin [160]. The other research showed in vivo studies of luteolin suppressed lung metastasis of TNBC in MDA-MB-231 (4175) and MDA-MB-435 cell lines LM2 with concentrations of 40 mg/kg and 20 mg/kg, respectively. Luteolin significantly inhibited tumor cell migration to reduce VEGF levels and block VEGF receptors, with IC 50 of 10 µM in vitro and in vivo [161]. In addition, luteolin from Taraxacum officinale extract can inhibit Nrf2 in breast cancer stemness (Cripto1, CD44, ALDH1, ABCG2, NANOG, OCT4, and Sirt3) and chemoresistance, with IC 50 value 1 µM in an MDA-MB-231 cell line in vitro study [162]. JAK, Glycoprotein NMB (GpNMB), and hedgehog pathways. Here, we highlight the potential of using phytochemicals (luteolin, α-mangostin, piperine, silibinine, apigenin, quercetin, fisetin, resveratrol, genistein, 10-gingerol, chalcones, berberine, curcumin, epigallocatechin gallate, cyanidin-3-o-glucoside, and glycyrrhizin) in the treatment of TNBCs and their mechanisms of action. These natural compounds were collected after a thorough search of reports and studies on the Internet and in databases. Bioactive compounds from different sources in various plants are shown in Figure 3.

α-Mangostin
α-mangostin is isolated from Garcinia mangostana Linn with the mechanism of action as anti-proliferation, apoptosis, suppressed angiogenesis, and metastases [163]. According to a study in 2018, α-mangostin could significantly reduce the development of the spheroids in an MDA-MB-231 cell line, with an IC 50 value of 1.25 µg/mL. This finding points to a novel anti-cancer property of α-mangostin that could be used to improve conventional drug penetration into tumor bulk [164]. Another research reported that α-mangostin suppressed the proliferation, migration, and invasion of the PI3K/Akt signaling pathway by targeting RXRα and cyclin D1 in vitro and in silico studies. This compound was inhibited in the MDA-MB-231 cell line, with an IC 50 value of 11.37 µM [165].

Silibinin
Silibinin is a major bioactive flavanone. It has biological activity in a variety of cancer models such as breast and lung cancers by inhibiting cell proliferation, invasion, and angiogenesis. In the research using Hs578T, MDA-MB-231, BT474, T47D, HCC1806, and HCC1143 cell lines, silibinin significantly decreased TGF-β2-induced FN, MMP-2, and MMP-9 expression levels and suppressed the lung metastasis of TNBC cells. It also decreased TGF-β2 mRNA expression levels but not that of TGF-β1 in TNBC cells, and cell migration, as well as basal fibronectin and MMP-2 expression levels, decreased as well in response to silibinin in vitro and in vivo studies with the IC 50 value of 50 µM [166]. Another study reported that silibinin inhibited the gene-specific transcriptional activation of MMP-2 expression and suppressed the phosphorylation of the Jak2/STAT3 signaling pathway by blocking the STAT3 nuclear translocation and DNA-binding activity, resulting in reduced cell migration and invasion with the IC 50 value of 200 µM in MDA-MB-231 cell line [168].

Apigenin
Apigenin is a natural flavonoid compound and has an effect on diabetes, amnesia and Alzheimer's disease, depression, insomnia, and cancer [169]. Apigenin is found to be able to decrease the expression of target genes, such as CTGF and CYR61 and YAP/TAZ

Quercetin
Quercetin is a plant-derived flavonoid found in fruits, vegetables, and tea, which is known to have multiple biological actions such as antioxidant, anti-inflammatory, and anti-cancer. Quercetin induces apoptosis and cell cycle arrests by modulation of Foxo3a activity and inhibition of JNK activity that reduced the signaling activities of p53, p21, and

Fisetin
Fisetin is one of the major flavonoids from many fruits and vegetables such as strawberries, apples, persimmons, grapes, onions, and cucumbers [174]. Fisetin dose-dependently inhibits cell proliferation, migration, and invasion in MDA-MB-231 and BT549 cells. In vitro assay demonstrated that fisetin suppressed phosphoinositol 3-kinase (PI3K)/Akt/GSK-3β signaling pathway but upregulated the expression of PTEN mRNA and protein in a concentration-dependent manner. On the other hand, in vivo tests, with a concentration of 100 mg/kg, indicated that fisetin could inhibit the growth of primary breast tumors and reduce lung metastasis while increasing the expression of EMT molecules and PTEN/Akt/GSK-3β with an IC 50 value of 100 µM [175].

Resveratrol
Resveratrol is a non-flavonoid polyphenolic compound from wine and grape juice, also synthesized in grape leaves and grape skins. It is reported that resveratrol promoted the apoptosis of TNBC cells by reducing POLD1 expression, thereby activating the respective apoptosis pathways in the MDA-MB-231 cell line by in vitro and in vivo assays having an IC 50 value of 50 µM [176]. Another research reported that resveratrol at an IC 50 value of 185 µM combined with 14 µM cisplatin inhibited fibronectin, vimentin, PI3K/Akt, Smad2, Smad3 JNK, ERK, Nf-K B expressions by TGF-β1, and increasing E-cadherin expression. This compound can also inhibit migration, invasion, and tumor growth within in vitro and in vivo studies in MDA-MB-231 [177].

Genistein
Genistein (Gen) is a natural isoflavone with biological activities such as anti-breast cancer [178]. In a dose-dependent manner, genistein induced apoptosis and cell cycle arrest in the G2/M phase. Gen inhibited NF-κB activity by the Nocth-1 signaling pathway, as well as downregulated cyclin B1, Bcl-2, and Bcl-xL expression in the MDA-MB-231 cell line at an IC 50 value of 20 µM. Further preclinical and clinical studies are warranted to investigate the application of Gen for the treatment of TNBC [179]. Other research showed that Gen inhibited CDK1 kinase activity by phosphorylation on the Thr14 and Tyr15 sites by inducing G2/M cell cycle arrest, apoptosis, and DNA damage response pathways such as ATR and BRCA1 activation. An IC 50 value of 40 µM was present in the MDA-MB-231 cell line [180].

(10)-Gingerol
(10)-gingerol is found in ginger (Zingiber officinale Roscoe) oleoresin from a fresh rhizome. The results reported that (10)-gingerol induced metastatic dissemination, including lung, bone, brain, and apoptosis death in mouse and human TNBC (MDA-MB-231) cell lines in vitro and in vivo. It also inhibited 4T1Br4 orthotopic tumor growth, with a concentration of 10 mg/kg in the in vivo study. Furthermore, the in vitro study obtained the IC 50 value of 100 µM in the MDA-MB-231 cell line [181]. The other research showed inhibited mitogen-induced activation of Akt and p38MAPK and the suppressing of epidermal growth factor receptor expression. The result reported cell migration and invasion through the suppression of MMP-2 activity, with an IC 50 value of 10 µM in the MDA-MB-231 cell line by in vitro study [182].

Chalcones
Chalcones is a natural flavonoid from many flowers and plants, including fruits and vegetables [183,184]. It has pharmacological activities such as hypertension, infectious diseases, neurological disorders, and cancer [185]. Chalcone, extracted from Cardamonin, induces invasive, migration, and reverses epithelial-mesenchymal transition (EMT) by downregulation of Wnt/β-catenin signaling in BT-549 and MDA-MB-231 cell lines. This result significantly inhibits the phosphorylation of GSK3-β by inhibiting Akt activity. The in vitro study and concentration of 5 mg/kg in vivo study had an IC 50 value of 20 µM in BT-549 and MDA-MB-231 cell lines [186].

Berberine
Berberine is a natural isoquinoline alkaloid compound isolated from the stems and roots of plants such as Berberis vulgaris, Berberis asiatica, Berberis aristata, Coptidis japonica, Coptidis japonica, Coptidis rhizome, Coptidis chinensis, Mahoniaaqui folium, and Mahonia beale [187,188]. Berberine significantly induced apoptosis and had the most sensitive reaction to HCC70, BT-20, and MDA-MB-468 cell lines, with IC 50 values of 0.19 µM, 0.23 µM, and 0.48 µM, respectively. Berberin also induced cell cycle arrest at G1 and/or G2/M phases in MDA-MB-468 and HCC70 cell lines and S phase in BT-20 cell line. Berberine induced apoptosis with an IC 50 value of 1 µM in all of the cell lines by in vitro study. The research suggests berberine as a potential candidate for TNBC therapy [189].

Curcumin
Curcumin induces apoptosis and decreased expression levels of extracellular regulated protein kinase (ERK1/2), pERK1/2, EGFR, and pEGFR in MDA-MB-231 cells [190]. The research suggested curcumin as a potential anti-TNBC due to its ability to promote apoptosis, and to block the cell cycle of TNBC cells (MDA-MB-231) by inhibiting restoring DLC1 and EZH2 expression; it also inhibited the migration, invasion, and proliferation in vitro and in vivo studies with an IC 50 value at 40 µM for both MDA-MB-231 and MDA-MB-468 cell lines [191]. Other research showed that curcumin inhibited the SIK3-mediated cyclin D upregulation in the G1/S cell cycle and inhibited cell growth during epithelial-mesenchymal transition (EMT), with an IC 50 value of 25 µM in the MDA-MB-231 cell line by in vitro and in vivo studies [192].

Epigallocatechin Gallate
Epigallocatechin gallate (EGCG) is a major natural component of green tea. EGCG has been evaluated in some clinical trials. It has been reported that Epigallocatechin gallate suppressed the growth, migration, and invasion of TNBC cells by inhibiting VEGF gene expression in the Hs578T cell line [193]. Wnt/β-catenin activation was downregulated by EGCG. However, upregulation of Wnt/β-catenin extinguished the inhibitory effects of EGCG on lung cancer [194]. Wnt/β-catenin signaling was suppressed by EGCG by promoting GSK-3β and PP2A-independent phosphorylation/degradation of β-catenin with the IC 50 value of 80 µM [195]. Hong et al. (2017) reported that EGCG can also inhibit the β-catenin pathway, phosphorylation of Akt, and cyclin D1 expression, with an IC 50 value of 200 µM in the MDA-MB-231 cell line [196]. Other research showed that the synthesis of EGCG analogues are diesters (G28, G37, and G56) and monoesters (M1 and M2) inhibiting the lipogenic enzyme fatty acid synthase (FASN) with an IC 50 value of 1.5 µM in the MDA-MB-231 cell line [197].

Glycyrrhizin
Glycyrrhizin is a natural compound from licorice root and its metabolite, glycyrrhetinic acidis, is potent against TNBC by inhibiting cell proliferation. Glycyrrhetinic acid exhibits a synergistic effect of etoposide and upregulation of TOPO 2A with an IC 50 value of 20 µM in MDA-MB [200]. The other research showed that glycyrrhizic acid from licorice root extracts inhibited intracellular and reactive oxygen species-mitochondrial, cell death, and autophagy by the nuclear translocation of apoptosis-inducing factors (AIF) and LC-3 in the MDA-MB-231 cell line, with an IC 50 value of 20 µM in vitro study [201].
Some of the natural compound's activities and its mechanism are summarized in Table 2.  In vitro and in silico [206] A sequesterpenoid from Farfarae Flos (Tussilago farfara)

MDA-MB-231
and MCF-7 Induced endoplasmic reticulum stress and autophagy by fatty acid synthase inhibition mediated apoptosis In vitro [222] 4.18. Schisandrin A Schisandrin A, a bioactive phytochemical, is one of the representative lignans species from the fruit of Schisandra chinensis Turcz. (Baill.). It has biological activity such as antiinflammation and anti-oxidative stress [223]. A study found that Schisandrin

Naringin/Flavonoid
Naringin is a flavonoid compound specifically of the flavanone subgroup. This compound of purity ≥95% uses HPLC. Naringin can induce G1 cell cycle arrest, inhibit cell proliferation, and promote cell apoptosis by regulating p21, survivin, and suppressed β-catenin signaling pathway with IC 50

Cryptotanshinone
Cryptotanshinone is a bioactive component from the dried roots of Salvia miltiorrhiza Bunge (Danshen) that is purified by normal-phase silica gel column chromatography followed by preparative TLC [224].

Curcuma longa
Curcumin from rhizomes of Curcuma longa (C1386, purity >65%) was purified by column chromatography on silica gel using CHCl 3 /hexane 90:10 as eluent using TLC for monitoring the reaction. The result showed that analog curcumin (1-3) compounds can decrease the activity of the NF-κB transcriptional factor. The compounds inhibited TNBC cell lines with IC 50 values of 1.30, 1.59, and 0.88 µM in the SUM149 cell and 0.41, 0.00, and 0.85 in MDA-MB-231, respectively, compared to curcumin [213].

Ganoderma lucidum
Ganoderma lucidum is a medicinal mushroom with anti-cancer activity. It was found to reduce cell adhesion, proliferation, survival, invasion, and downregulation of the STAT3 pathway. Ganoderma lucidum decreases the STAT3 pathway and the expression of OCT4, NANOG, and SOX2 in vitro, as well as in vivo on injected limiting dilutions (CD44+/CD24-) tumor models with IC 50 values of 0.50 mg/mL in SUM-149 and 0.96 mg/mL in MDA-MB-231 cells [214].

Astragalus membranaceus
Astragalus membranaceus major components are comprised of polysaccharides, flavonoids, and saponins with a purity of 98%. It has pharmacology activities, such as immunomodulating, anti-oxidant, and anti-inflammatory [225]. The in vitro study reported that Astragalus polysaccharides inhibited the proliferation, invasion, and apoptosis of cell lines by the PIK3CG/AKT/BCL2 pathway, with an IC 50 value of 2 mg/mL in MDA-MB-231 [216].

Eupalinolide J
Eupalinolide J is a new sesquiterpene lactone isolated from Eupatorium lindleyanum DC. It has various biological activities, including anti-inflammatory [226], anti-cancer [227], and anti-oxidant activities [228]. The purity of Eupalinolide J was above 95%. Eupalinolide J suppressed tumor growth by STAT3 signaling pathways in vitro and in vivo in the mouse xenograft model which induces apoptosis, mitochondrial membrane potential (MMP) disruption, proliferation, and cell cycle arrest at the G2/M phase. The IC 50 values were 0.58 in MDA-MB-231 and 0.39 µM in MDA-MB-468 cells [218].

Chantaridin
Chantaridin is a terpenoid compound from the blister beetle Mylabris phalerata (Pallas). Chantaridin inhibited cell proliferation by inducing apoptosis and inhibiting autophagy, additionally leading to the conversion of LC3-I to LC3-II with suppressed Beclin-1 expression in vitro using flow cytometry and in vivo using nude mice of tumor xenograft with a dose of 10 mg/kg. The IC 50 value is 5 µg/mL in MDA-MB-231 and MDA-MB-468 TNBC cell lines [219,229].

Cucurbitacin E
Cucurbitacin E was isolated from Hemsleya delavayi var. yalungensis (Cucurbitaceae). This compound was extracted with methanol followed by purification using silica gel column chromatography by monitoring TLC and spectroscopic. Cucurbitacin E has been reported to significantly decrease cell viability by inducing cell cycle G2/M phase arrest, decreased expression of cyclin D1, survivin, XIAP, Bcl-2, and Mcl-1 and increased activation of JNK, as well as inhibited AKT and ERK activation. The reported IC 50

Future and Prospects
TNBC is a type of tumor that is aggressive when it comes to metastasis and has a poor prognosis. Medication has a low clinical benefit in TNBC patients, therefore, finding molecular targets for TNBC treatment is essential for acquiring appropriate therapeutic targets. Several pathways can be targeted, including BRCA, Wnt/β-catenin, NF-κB, Hedgehog, JAK, PD-1/PD-L1, PI3K/Akt/m-TOR, EGFR [230,231], and others that have long been part of the treatment strategy. Finding new and effective treatment options for TNBC remains a critical clinical need. To enhance TNBC survival and treatment, a greater understanding of the molecular basis of heterogeneity and the development of improved therapeutic strategies are necessary.
The Wnt/β-catenin signaling pathway is one of the molecular targets in TNBC [232] that is currently being investigated. Wnt activation can cause β-catenin accumulation in the nucleus. It can activate TCF/LEF-1, which promotes the transcription of target genes, thus a molecular understanding of the Wnt/β-catenin pathway is required for suppressing the metastatic pathway in TNBC. To develop more effective drugs, new experimental approaches should be tested in patients with TNBC. Several approaches to TNBC therapy include targeted DNA repair (platinum compounds and taxanes) [233], p53 (taxanes) [234], cell proliferation (anthracycline-containing regimens) [235], and targeted therapy. The best adjuvant regimen for TNBC is still being developed [235].
As shown in Figure 4, several signaling pathways are associated with genetic mutations in cancer, including the upregulation of the Wnt pathway and growth factors such as EGFR leading to cancer growth, metastasis, cell proliferation, invasion, differentiation, angiogenesis, and apoptosis. Inhibition of the Wnt pathway by inhibitors (bioactive compounds or plant extracts) begins when the Wnt ligand binds to the frizzled main receptor (FZD) and co-receptor LRP5/6 (LRP). The binding of the Wnt ligand to its receptor during signaling leads to disruption of LRP phosphorylation by inhibitors (red and blue boxes) and disheveled inactivation. As a result, the action of AXIN and APC to bind to LRP GSK-3β is inhibited and β-catenin is retained because it is not phosphorylated by GSK-3β. This causes the inactivation of TCF/LEF gene transcription. Inhibition of PI3K/Akt/m-TOR and JAK/STAT3 by bioactive compounds or plant extracts results in the prevention of cell proliferation, invasion, and survival in the EGFR growth pathway. Thus, the degradation of cyclin D1 occurs after being induced by bioactive compounds to encourage the inactivation of Wnt/β-catenin.
Natural substances may be useful in the treatment of breast cancer. Based on previous studies, we resumed the involvement of bioactive compounds and plant extracts to inhibit targets involved in TNBC regulation as shown in Figure 4. In this review, we only explored the natural compounds from extracts and isolates that have an effect on TNBC cell lines in in vivo, in vitro, and in silico studies. Other compounds from natural products are still needed for TNBC treatment agents, thus further developments should be carried out using compounds such as luteolin, α-mangostin, piperine, silibinine, apigenin, quercetin, fisetin, resveratrol, genistein, 10-gingerol, chalcones, berberine, curcumin, epigallocatechin gallate, cyanidin-3-o-glucoside, and glycyrrhizin. The potential oncogenic molecular pathways in TNBCs were discussed, as well as how the dose and purified plant-derived natural compounds selectively target and modify the genes and/or proteins implicated in these aberrant mechanisms to demonstrate anti-cancer potential. The mechanism of action of each natural compound component varies according to the influence of dose, purity, and isolation. Furthermore, the IC 50 value of natural compounds that inhibits TNBC also influences their mechanisms. One of the chemical components having the potential as a TNBC therapeutic agent is α-mangostin isolated from the mangosteen rind (Garcinia mangostana L.). α-mangostin has been shown to suppress the MDA-MB-231 and TNBC cell lines, as well as tumor development and metastasis in a mouse breast cancer model. Therefore, understanding the characteristics of TNBC is critical in identifying effective treatment targets for the development of aggressive TNBC, particularly the metastatic route via the Wnt/β-catenin pathway. Natural substances may be useful in the treatment of breast cancer. Based on previous studies, we resumed the involvement of bioactive compounds and plant extracts to inhibit targets involved in TNBC regulation as shown in Figure 4. In this review, we only explored the natural compounds from extracts and isolates that have an effect on TNBC cell lines in in vivo, in vitro, and in silico studies. Other compounds from natural products are still needed for TNBC treatment agents, thus further developments should be carried out using compounds such as luteolin, α-mangostin, piperine, silibinine, apigenin, quercetin, fisetin, resveratrol, genistein, 10-gingerol, chalcones, berberine, curcumin, epigallocatechin gallate, cyanidin-3-o-glucoside, and glycyrrhizin. The potential oncogenic molecular pathways in TNBCs were discussed, as well as how the dose and purified plant-derived natural compounds selectively target and modify the genes and/or proteins implicated in these aberrant mechanisms to demonstrate anti-cancer potential. The mechanism of action of each natural compound component varies according to the influence of dose, purity, and isolation. Furthermore, the IC50 value of natural compounds that inhibits TNBC also influences their mechanisms. One of the chemical components having the potential as a TNBC therapeutic agent is α-mangostin isolated from the mangosteen rind (Garcinia mangostana L.). α-mangostin has been shown to suppress the MDA-MB-231 and TNBC cell lines, as well as tumor development and metastasis in a mouse breast cancer model. Therefore, understanding the characteristics of TNBC is critical in identifying effective treatment targets for the development of aggressive TNBC, particularly the metastatic route via the Wnt/β-catenin pathway.

Conclusions
Chemotherapy or radiotherapy is a common treatment for triple-negative breast cancer; however, it has various side effects such as the occurrence of resistance, narrow therapeutic index, and unselective action of anti-cancer drugs damaging the DNA of cancer cells and regular cells. Numerous studies are being conducted to develop new medicines that are more effective against cancer cells and have fewer adverse effects. Exploring molecules derived from natural sources as anti-cancer treatment agents is one of the potential research avenues. This has led to an alternative therapeutic approach for TNBC using natural compounds.
Many plant-derived natural compounds, including luteolin, α-mangostin, piperine, silibinin, apigenin, quercetin, fisetin, resveratrol, genistein, 10-gingerol, chalcones, berberine, curcumin, epigallocatechin gallate, cyanidin-3-o-glucoside, and glycyrrhizin, have shown anti-cancer properties, especially in the treatment of TNBCs. These compounds exhibit the capability to suppress cell growth, migration, and metastasis by targeting irregular/irregular signaling pathways present in TNBC, such as Wnt/β-Catenin, NF-κB, PI3K/Akt/mTOR, PD-1/PD-L1, LAG-3, CTLA-4, STAT-3, EGFR, Trop-2, RAF/MEK/ERK, JAK, Glycoprotein NMB (GpNMB), and hedgehog pathways. Despite the fact that the natural molecule shows potential against TNBC cell lines, compounds derived from natural resources are currently limited in their usage as TNBC therapeutic agents. Further research on the composition of substances derived from natural resources is needed to determine potential therapeutic candidates and histological characteristics. Data from these studies could provide insight into potential sources of natural compounds that could be used against the aggressive TNBC cells, particularly the metastatic pathway, in a targeted and effective manner.