Novel Insights into the Role of Chromatin Remodeler MORC2 in Cancer

Abstract

A newly discovered chromatin remodeler, MORC2, is a Microrchidia (MORC) family member. MORC2 acts as a chromatin remodeler by binding to the DNA and changing chromatin conformation using its ATPase domain. MORC2 is highly expressed in a variety of human cancers. It controls diverse signaling pathways essential for cancer development through its target genes and interacting partners. MORC2 promotes cancer cells’ growth, invasion, and migration by regulating the expression of genes involved in these processes. MORC2 is localized primarily in the nucleus and is also found in the cytoplasm. In the cytoplasm, MORC2 interacts with adenosine triphosphate (ATP)-citrate lyase (ACLY) to promote lipogenesis and cholesterogenesis in cancer. In the nucleus, MORC2 interacts with the transcription factor c-Myc to control the transcription of genes involved in glucose metabolism to drive cancer cell migration and invasion. Furthermore, MORC2 recruits on to the promoters of tumor suppressor genes to repress their transcription and expression to promote oncogenesis. In addition to its crucial function in oncogenesis, it plays a vital role in DNA repair. Overall, this review concisely summarizes the current knowledge about MORC2-regulated molecular pathways involved in cancer.

1. Introduction

Chromatin remodelers govern various cellular functions, such as transcription, DNA replication, and DNA repair mechanisms, by regulating the access to genomic DNA for the protein complexes that regulate these processes [1,2,3,4]. The chromatin remodelers, typically are ATP-dependent, regulate DNA accessibility to the DNA-binding proteins by ejecting, altering, or repositioning the nucleosomes [2,5,6]. This ensures cellular identity determination and normal cell function [2]. The deregulated expression of chromatin remodelers leads to altered chromatin structure and gene expression, which promotes cancer and other diseases [1,7,8,9,10,11,12]. Therefore, knowledge about the effects and significance of the chromatin remodeling families and complexes is emerging.

One of the emerging chromatin remodeling family members in eukaryotes is Microrchidia (MORC). MORCs are widely expressed and play an important role in chromatin remodeling and epigenetic control [13]. For the first time, Watson and others discovered an insertional mutation (morcTgN (Tyr)1Az) in Morc1 in mice, and they demonstrated that this Morc1 mutation is responsible for inhibiting spermatogenesis and germ cell death [14]. While Morc -/- female mice were normal, Morc -/- male mice were found to be infertile with diminished testicular mass [14]. This suggests that the MORC gene has specific functions and is essential for male gametogenesis. Five MORC family members were identified in humans: MORC1, MORC2, MORC3, MORC4, and a divergent SMCHD1 (Structural Maintenance of Chromosomes Flexible Hinge Domain 21 containing 1) [13]. MORC family members have different biological activities but a typical domain architecture (CW-type zinc finger, GHKL-ATPase, and coiled-coil domains) [15]. These family members were further divided into two subfamilies based on the structure of the ZF-CW domain, where MORC1 and MORC2 were placed in subfamily-I and MORC3 and MORC4 were placed in subfamily-IX [16].

The human MORC family members express differentially in various tissues, supporting multiple biological functions. For instance, MORC1 expression has been detected in thymocytes, embryonic stem cells, and reproductive tissues such as the testis and is majorly involved in spermatogenesis [17,18]. MORC2 protein is expressed ubiquitously [17,18]. Low MORC2 protein expression levels have been observed in the hematological, immunological, secretory, and reproductive systems, whereas the liver and kidney have shown strong MORC2 protein expression [18]. MORC2 was shown to have potential role in gene transcription, DNA damage repair process, and adipogenic differentiation (18). MORC3 protein localization is restricted to the blood, immunological, secretory, and reproductive systems. MORC3 is involved in the transcriptional repression of genes and regulating calcium and bone homeostasis [18]. Meanwhile, MORC4 expression has been found in the placenta and testis and is involved in spermatogenesis [17,18].

MORC family members are highly dysregulated in various clinical conditions, including cancers, neurological illnesses, and metabolic bone diseases [18]. Among the MORC family members, MORC2 has a unique position due to its overexpression or deregulated expression in a wide range of human cancers and its function in the transcriptional regulation of genes involved in oncogenesis, DNA damage response, promoting cancer cell invasion, migration, cancer metabolism, metastasis, and chemoresistance (Figure 1). In this review, we emphasize the current developments in our knowledge of MORC2’s role as a transcriptional regulator, its post-translational modifications (PTMs), and its functions in regulating hallmarks of cancer.

2. MORC2 Domain Organization and Structure

The human MORC2 gene is at position q12.2 on the reverse strand of chromosome 22. So far, two functional protein coding MORC2 isoforms have been identified. MORC2 isoform-1 and 2 contain 1032 and 970 amino acids (a.a.), respectively. The transcript variant that codes for 970 a.a. isoform 2 (Uniprot ID: Q9Y6X9-2) has an additional exon, which results in the use of an in-frame downstream start codon, compared to the transcript variant 1 that codes for 1032 a.a. isoform (Uniprot ID: Q9Y6X9-1). This difference results in a shorter N-terminus compared to isoform-1. Although both MORC2 isoforms have different numbers of amino acids, their ATPase domain remains functionally active. The basic structure of MORC2 consists of a GHKL-ATPase (gyrase; heat shock protein, HSP 90; histidine kinase; DNA mismatch repair, Mut L) domain, zinc finger (ZF)-CW domain, coiled-coil domains, proline-rich domain (PRD), and chromo-like domain (CLD) (Figure 2).

The GHKL-ATPase domain is necessary for MORC2 to function as an ATPase, and as a result of this function, MORC2 regulates chromatin remodeling in response to DNA damage [20]. The transcription activation suppressor (TASOR), M-phase phosphoprotein 8 (MPP8), and periphilin are components of the Human Silencing Hub (HUSH) complex [26]. Periphilin binds to RNA and directs HUSH to its target loci, where HUSH recruits the Su(var)3-9, enhancer of zeste and trithorax (SET) domain bifurcated histone lysine methyltransferase 1 (SETDB1), MORC2, and nuclear exosome-targeting (NEXT) complex. SETDB1 deposits histone 3 lysine 9 trimethylation (H3K9me3). MPP8 recognizes H3K9me3 and allows the HUSH complex to bind at the locus to repress the gene transcription. It has been demonstrated that MORC2′s ATPase domain is necessary for the functions of the HUSH complex [26]. The ZF-CW domain is a reader domain with a comparatively short motif of 50–60 amino acids. This domain contains four conserved cysteines (C) and two conserved tryptophan (W) residues, which can bind to zinc to form finger-like projections, enabling them to interact with the target genes that participate in processes such as the recognition of methylated histones, chromatin remodeling [27], epigenetic control, and embryonic development [28]. However, functionally, the MORC2 ZF-CW domain is not well characterized. The coiled-coil domain plays a significant role in nucleic acid binding, protein stability, assembly, and protein–protein interactions [29,30,31,32,33]. The MORC2 protein includes five coiled-coil domains in total, allowing MORC2 to dimerize. The dimerization of MORC2 is a critical event in the initiation of DNA repair signaling in response to DNA damage [30]. Although MORC2 has several coiled-coil domains, each domain interacts with different partners for a specific function. The coiled-coil domain 1 of MORC2 interacts with chromatin by binding to DNA, whereas the C-terminal coiled-coil domains aid in dimerization, which is important for its contributing functions, such as DNA-damage repair and cell survival [30,34]. In addition to the common MORC protein domains, MORC2 has a PRD (proline-rich domain) and a CLD (chromo-like domain) [13]. The PRD domain of MORC2 interacts with a cadherin-associated protein, catenin delta 1 (CTNND1), to promote tumor invasion and metastasis [35]. The MORC2-CLD function is still unknown. Additionally, the MORC2 protein also has one putative bipartite and two putative monopartite Nuclear Localization Signals (NLSs), which lie between 657 and 781 a.a., and a further Nuclear Export Signal (NES), which lies between 481 and 657 a.a. Both the NLSs and NES facilitate MORC2 to become localized in the nucleus and cytoplasm, respectively. Wang et al. experimentally showed that most of the MORC2 protein is located in the nucleus rather than in the cytoplasm and concluded that this might be due to the fact that NLSs are more prevalent than NESs [36]. External cues, such as stress, growth factors, cytokines, etc., regulate the localization of MORC2 [17,18,20,35]. However, the shuttling of MORC2 between intracellular spaces is still an unventured question to solve.

3. MORC2 Is a Transcriptional Regulator

In response to upstream signaling molecules such as growth factors, cytokines, metabolites and radiation, chromatin remodelers, and chromatin modifiers regulate the expression of target genes implicated in cancer progression and metastasis. Due to its ATPase activity, MORC2 changes the conformation of the chromatin in an energy-dependent manner [34]. Additionally, MORC2 associates with transcription factors or histone deacetylases (HDACs) to coordinate the expression of target genes implicated in metabolism and cancer progression (Figure 3). As shown below, it acts as an activator or a repressor to control the transcription of target genes involved in cancer.

3.1. MORC2 Acts as a Transcription Repressor

MORC2 contributes to target gene transcription because of the CW zinc finger motif. Shao et al. identified carbonic anhydrase IX (CAIX) as the target gene of MORC2 using DNA microarray hybridization and northern and western blot analyses [19]. CAIX was the first target gene of MORC2 to be discovered [19]. In various human cancers, including those of the cervix, breast, head and neck, lung, and brain, overexpression of CAIX has been noted [37]. CAIX promotes tumorigenesis and invasion upon CAIX overexpression [38]. Furthermore, the overexpression of CAIX is also associated with poor prognoses [39]. According to Shao et al.’s research [19], MORC2 and HDAC4 are recruited to the CAIX promoter, repressing CAIX gene transcription. Based on these observations, it was concluded that MORC2 binds to the CAIX promoter first, then recruits HDAC4, which decreases the histone H3 acetylation status of the CAIX promoter, causing the chromatin to close and suppressing CAIX expression [19]. From 2010 onwards, several studies provided insights on MORC2 transcriptional repressor functions, where MORC2 decreased the expression of p21Waf/Cip1 (p21), arg-binding protein 2 (ArgBP2), N-myc Downstream-Regulated Gene 1 (NDRG1), neurofibromatosis 2 (NF2), and kidney- and brain-expressed protein (KIBRA) (Figure 3). The CDK inhibitor p21 is a crucial regulator of cell survival and proliferation [40]. Zhang et al. [41] and Ou, Kepeng et al. [42] found that MORC2 expression is inversely correlated with p21 expression in individuals with gastric and colorectal cancers, respectively. Zhang et al. also discovered that MORC2 and HDAC1 are recruited onto the p21 promoter to repress its expression in a p53-independent manner. The MORC2-mediated p21 repression enhances cell cycle progression, resulting in alterations in the cell cycle, as seen by a decreased percentage of G1 phase cells and an increased percentage of S and G2/M phase cells. Further, they also discovered that MORC2 enhances gastric cancer cell proliferation by controlling cell cycle progression via p21 suppression [41]. Kepeng et al. analyzed the RNA sequence and clinical data from colorectal cancer (CRC) patients in the TCGA data base, and they identified elevated MORC2 levels. By performing CCK8 and colony formation assays under the conditions of MORC2 knockdown, they found that MORC2 has a role in CRC proliferation. They observed a positive correlation between the expression levels of p53 and p21 along with the proinflammatory cytokines IL-6 and IL-8 responsible for cellular senescence via decreasing the expression of HDAC4. Based on these findings, they concluded that increased MORC2 plays a key role in CRC tumorigenesis by controlling cellular senescence [42]. ArgBP2 controls the reorganization of the actin cytoskeleton [43]. Tong et al. [44] discovered low expression levels of ArgBP2 mRNA in gastric cancer tumor samples. They identified that ArgBP2 overexpression inhibits the proliferation, invasion, and migration of gastric cancer cells. They identified ArgBP2 as a target gene of MORC2. They demonstrated that MORC2 enhances the enhancer of zeste homolog 2 (EZH2), a polycomb repressive complex 2 (PRC2) subunit recruitment onto the ArgBP2 promoter, which promotes tri-methylation of H3K27 and thereby represses ArgBP2 transcription. Due to this, there is low-level expression of ArgBP2 in gastric cancer cells, which is responsible for gastric cancer cell proliferation [44]. Alternatively, MORC2 also represses ArgBP2 transcription by enhancing the recruitment of heat shock factor protein 1 (HSF1) and PRC2 onto the ArgBP2 promoter [45]. NDRG1 is a metastasis suppressor and prognostic colorectal cancer (CRC) biomarker. Liu et al. [46] identified that MORC2 downregulates NDRG1 expression in CRC cells and observed a negative correlation between MORC2 and NDRG1 in CRC patients. They found that MORC2 interacts with sirtuin1 (SIRT1) and gets recruited onto the NDRG1 promoter to repress the transcription and expression of NDRG1. Furthermore, the increased expression levels of MORC2 and decreased expression of NDRG1 are associated with lymph node metastasis in CRC samples [46]. In addition, Wang et al. [47] reported that MORC2, along with DNA methyltransferase 3A (DNMT3A), represses NF2 and KIBRA expression by recruiting onto their promoters to facilitate tumorigenesis and cancer stemness in hepatocellular carcinoma.

3.2. MORC2 Acts as a Transcription Activator

Based on the signal, MORC2 protein, in association with transcription factors or coactivator complexes, regulate/or activate the target gene’s transcription in a promoter context-dependent manner. So far, MORC2 has been found to act as a transcriptional coactivator for activating the transcription of the genes lactate dehydrogenase A (LDHA), Connective Tissue Growth Factor (CTGF), and Snail Family Transcriptional Repressor 1 (SNAIL) [23,24]. LDHA is the key enzyme involved in this process, where it converts pyruvate to lactate even in the presence of oxygen in cancer cells. Guddeti et al. [23] demonstrated that MORC2 is a glucose-inducible gene and a transcriptional target gene of c-Myc. Cancer cells treated with a high glucose concentration induce the expression of MORC2, which interacts with c-Myc and gets recruited onto the LDHA promoter to increase the transcription of LDHA. Additionally, they demonstrated that the MORC2–c-Myc–LDHA signaling axis contributes to the migration of breast cancer cells [23]. This was the first study to describe MORC2’s role as a transcription activator in breast cancer cells in association with the transcription factor c-Myc.

Further, Liu et al. [24] discovered that the Transforming Growth Factor β1 (TGF-β1) target genes CTGF and SNAIL, are also transcriptionally activated by MORC2 (O-GlcNAcylated MORC2). TGF-β1 signaling aids in the progression of breast cancer by controlling the transcription of the genes SNAIL and CTGF, which have a proven role in tumor metastasis [48,49]. SNAIL is a potent inducer of breast cancer invasion and metastasis and a master regulator of TGF-β1-driven epithelial–mesenchymal transitions [50,51]. The migratory, invasive, metastatic, and angiogenic processes in human breast cancer cells are all significantly influenced by CTGF [52,53]. Liu et al. identified that O-GlcNActransferase (OGT) interacts with MORC2 and promotes the O-GlcNAcylation of MORC2. They found that glucose induces MORC2 O-GlcNAcylation in a dose-dependent manner in MCF-7 and T47D cells treated with glucose. Further, they tried to understand the role of TGF-β1 on MORC2 O-GlcNAcylation, as the growth factor influences the O-GlyNAcylation of proteins. They found that TGF-β1 induces the O-GlcNAcylation of MORC2 via increasing the stability of glutamine-fructose-6-phosphate aminotransferase (GFAT), which is needed for the synthesis of OGT. In addition, they noticed that O-GlcNAcylated MORC2 regulates the expression of SNAIL and CTGF by recruiting onto the promoters of SNAIL (−151 to −476) and CTGF (-1035 to -1235 and -1534 to -1925). Additionally, the knockdown of GFAT, SNAIL, or CTGF compromised the ability of TGF-β1-induced MORC2 O-GlcNAcylation-mediated breast cancer cell migration and invasion. They recognized that breast cancer patients with high-level expressions of MORC2, OGT, SNAIL, and CTGF had poor prognosis [24]. Overall, these findings establish that MORC2 regulates the TGF-β1 target genes SNAIL and CTGF transcriptionally [24].

4. MORC2 Post-Translational Modifications and Their Significance

Post-translation modification (PTM) plays an important role in regulating distribution of MORC2 function(s) in DNA damage response and cancer development. The first PTM discovered on a MORC2 protein was phosphorylation (Figure 4). Since then, diverse PTMs on MORC2 have been studied spanning the post-ATPase domain region. Upon genotoxic stress stimulations, MORC2 acts as a substrate for p21 activated kinase 1 (PAK1), N-acetyltransferase (NAT10), poly (ADP Ribose) polymerase 1 (PARP1), and tripartite motif-containing 28 (TRIM28) and becomes phosphorylated, acetylated, poly (ADP-ribosyl)ated, and SUMOylated [20,21,22,25]. DNA damage triggers MORC2 phosphorylation by PAK1, and further phosphorylated MORC2 recruits onto DNA damage sites and induces histone H2AX phosphorylation to facilitate chromatin-remodeling-mediated DNA repair [20]. MORC2, NAT10, and PARP1 also play a crucial role in genome surveillance as a complex [21,22,54]. NAT10 acetylates MORC2 at the lysine 767 residue (K767Ac). Acetylated MORC2 promotes cell survival by reducing the phosphorylation of the 11th threonine residue of the histone H3 protein (H3T11P), transcriptional repression of CDK1 and Cyclin B1, and subsequent G2 DNA damage checkpoint activation [22]. MORC2 acetylation and its role in DNA damage is further regulated by the PARP1-facilitated nucleoplasm translocation of the NAT10 enzyme [54]. At DNA damage sites, MORC2 is recruited by the PARP1 enzyme and gets PARylated [21]. MORC2 PARylation further facilitates the increased accessibility of damaged chromatin and, in turn, promotes PAR-dependent DNA repair by stabilizing the PARP1 protein from ubiquitination [21]. The response of DNA damage and MORC2 post-translational modifications is intriguingly regulated in a time- and damage-dose-dependent manner. At the late stages of DNA damage, MORC2 is SUMOylated by TRIM28 at K767, and the SUMOylated MORC2 activates DNA repair kinases, thereby promoting chromatin accessibility, DNA repair, and chemoresistance [25]. The MORC2 phosphorylation at Ser739 and acetylation at Lys767 regulate the SUMOylaiton status at Lys767 and exhibit negative crosstalk upon damage, respectively [25].

In addition to the role of MORC2 in DNA repair and response, MORC2 also plays a quintessential role in regulating cancer cell proliferation, such as (i) PAK1-mediated MORC2 phosphorylation, which is required to promote gastric cancer cell proliferation by facilitating G1–S transitions and (ii) O-GlcNAcylated MORC2, which is induced by TGF-β1 treatment, recruits TGF-β1 target genes (CTGF and SNAIL) and plays a requisite role in their transcriptional activation by an unknown mechanism, promoting breast cancer invasion and migration [24]. E2- and ESR1-targeting drugs mediate breast cancer proliferation by preventing MORC2 lysosomal degradation via chaperon-mediated autophagy [55]. An estrogenic receptor (GPER1) activates protein kinase cAMP-activated catalytic subunit alpha (PRKACA), which in turn phosphorylates MORC2 at Thr582 [55]. Phosphorylation reduces interactions with CMA machinery molecules (HSPA8 and LAMP2A), enhancing its stability and oncogenic activity [55]. Hu et al. identified that the microtubule-targeting drugs paclitaxel (PTX) and vincristine (VCR) promote CDK1-mediated MORC2 phosphorylation (T717 and T733), which causes MORC2 degradation through a chaperone-mediated pathway. Upon treatment with PTX and VCR, MORC2 degradation helps in prolonged mitotic arrest and the death of cancer cells [56]. The dynamic states of post-translationally modified MORC2 play a key role in mediating its protein turnover, resistance to DNA-damaging agents, cell survival, checkpoint activation, and genome integrity by chromatin remodeling and recruiting repair machinery.

5. MORC2 Role in Cancer

Nearly all the human cells and tissues were found to express the MORC2 protein [17,18]. MORC2 expression is very high in cancer cells compared to normal cells [18]. Several cancers, including breast, lung, liver, prostate, stomach, colon, ovarian, pancreatic, and endometrial, have dysregulated MORC2 expression [57,58]. This increased expression of MORC2 is linked to cancer cell proliferation, metabolism, invasion, migration, and metastasis and confers chemotherapy resistance [15,23,24,25,35,42,46,55,57,58,59,60,61,62,63,64]. Furthermore, increased MORC2 expression levels were linked to poor prognosis and unfavorable clinical outcomes in non-small cell lung and breast cancer [58]. Notably, MORC2 interacts with many proteins to control the expression of its downstream targets, which promote the hallmarks of cancer or directly modulate the hallmarks of cancer by regulating the transcription of its target genes [15,57].

MORC2 is overexpressed in colorectal cancer, and by controlling cellular senescence, it promotes tumorigenesis [42]. Saroha et al.’s [62] study revealed that MORC2 regulates β-catenin expression and function by modulating the phosphorylation of AKT. They noticed reduced proliferation and migration of MORC2-overexpressing breast cancer cells upon β-catenin inhibition. They concluded from these findings that MORC2 regulates β-catenin signaling to support breast cancer cell proliferation and migration [62]. By controlling the PTEN/PI3K/AKT signaling pathway, MORC2 promotes glioma cell proliferation, migration, invasion, and epithelial–mesenchymal transition (EMT) [60]. Additionally, Wang et al. demonstrated that PAK1-mediated phosphorylation of MORC2 promotes the growth and development of gastric cancer [65]. Wang et al. also discovered that MORC2, in collaboration with DNA methyltransferase 3A (DNMT3A), regulates the expression of NF2 and KIBRA to support carcinogenesis and cancer stemness in hepatocellular carcinoma [47]. Further, MORC2 interacts with EZH2 or HSF1 to control the expression of ArgBP2, which promotes the proliferation, invasion, and migration of cancer cells [44,45]. Furthermore, MORC2–SIRT1 complex suppresses NDRG1 expression to encourage metastasis in colorectal cancer [46]. Liao et al. showed that MORC2 interacts with catenin delta 1 (CTNND1) to promote invasion and metastasis in breast cancer [35]. Zhang et al. found that the mutant MORC2 (M276I) stimulates the splicing-based switch of CD44 from the epithelial isoform to the mesenchymal isoform in association with hnRNPM (heterogeneous nuclear ribonucleoprotein M), and this resulted in epithelial to mesenchymal transition [66].

The Warburg effect is a process whereby rapidly growing cancer cells consume large amounts of glucose and metabolize it by aerobic glycolysis [67,68,69]. It was discovered that MORC2 alters the metabolism of cancer cells by regulating glucose metabolism and lipogenesis [23,70,71]. The expression of MORC2 is induced with high glucose concentration in cancer cells. MORC2 then interacts with the transcription factor c-Myc and is recruited to the LDHA promoter to control the expression of LDHA, which is responsible for the migration of breast cancer cells [23]. Additionally, Guddeti et al. demonstrated that the MORC2–c-Myc–MAX complex regulates the expression of glycolytic enzymes and, thereby, breast cancer cell proliferation and migration [70]. Furthermore, Sanchez-Solana et al. reported that MORC2 interacts with adenosine triphosphate (ATP)-citrate lyase (ACLY), an enzyme that catalyzes the production of acetyl-CoA, which is a key metabolite for lipogenesis, cholesterogenesis, and histone acetylation [71]. Su et al. also showed that circDNM3OS increased MORC2 expression via sponging miR-145-5p, promoting glutamine metabolism and cholangiocarcinoma (CCA) [72].

Recently, several studies showed that MORC2 contributes to chemoresistance. By examining the expression levels of apoptosis-related proteins under MORC2 knockdown conditions, Pan et al. identified the mechanism through which MORC2 influences chemoresistance. The release of mitochondrial cytochrome c into the cytosol and the cleavage of caspase-9, caspase-3, and PARP were caused by MORC2 knockdown. These findings led them to the conclusion that MORC2 might be involved in chemoresistance [64]. In response to DNA damage, the SUMOylation of MORC2 orchestrates chromatin remodeling and DNA repair and promotes chemoresistance in breast cancer [25]. Yang et al. discovered that the phosphorylation of MORC2 in response to estrogen and antiestrogens inhibits CMA-mediated lysosomal degradation and plays a significant role in estrogen-induced proliferation and resistance to antiestrogen therapies in breast cancer [55]. The acetylation of MORC2 by NAT10 regulates cell-cycle check point control and resistance to DNA-damaging chemotherapy and radiotherapy in breast cancer [22]. Liao et al.’s investigation revealed that high MORC2 expression is a sign of worse neoadjuvant chemotherapy efficacy in triple-negative breast cancer (TNBC) [59].

6. Conclusions

A key member of the MORC chromatin remodeler family of proteins, MORC2 controls the expression of target genes linked to human cancer and neurological diseases. MORC2 biology has been the subject of significant scholarly investigation for approximately 20 years since its discovery. It is well known that MORC2 is involved in the control of several cancer-related functions. In this review, we outlined several transcriptional regulatory functions of MORC2 and post-translational modifications of MORC2 and their relevance to cancer. Overall, it is widely known that MORC2 plays a role in the DNA damage response and DNA repair mechanisms. It is exciting to know that MORC2 plays a crucial role in cancer metabolism, specifically in lipogenesis and glucose metabolism. Additionally, MORC2-driven signaling pathways support cell proliferation, invasion, migration, and metastasis. However, MORC2’s precise physiological activities in normal tissues are still unclear. The generation of MORC2 knockout mice, especially MORC2 liver knockout mice, is urgently required to comprehend the functional significance of MORC2 in metabolism and metastasis, as we and other studies reported that MORC2 has a role in glucose, glutamine, and lipid metabolism in cancer. Further, we are also interested in understanding MORC2 regulatory networks to develop MORC2-targeted anticancer therapeutics.