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Review
. 2024 Aug 8;41(9):221.
doi: 10.1007/s12032-024-02464-9.

Emerging roles of the chromatin remodeler MORC2 in cancer metabolism

Affiliations
Review

Emerging roles of the chromatin remodeler MORC2 in cancer metabolism

Bibhukalyan Mohapatra et al. Med Oncol. .

Abstract

Cancer is characterized by metabolic reprogramming in cancer cells, which is crucial for tumorigenesis. The highly deregulated chromatin remodeler MORC2 contributes to cell proliferation, invasion, migration, DNA repair, and chemoresistance. MORC2 also plays a key role in metabolic reprogramming, including lipogenesis, glucose, and glutamine metabolism. A recent study showed that MORC2-regulated glucose metabolism affects the expression of E-cadherin, a crucial protein in the epithelial-to-mesenchymal transition. This review discusses recent developments in MORC2 regulated cancer cell metabolism and its role in cancer progression.

Keywords: Glucose metabolism; Glutamine metabolism; Lipogenesis; MORC2.

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References

    1. Chutani N, Singh AK, Kadumuri RV, Pakala SB, Chavali S. Structural and functional attributes of microrchidia family of chromatin remodelers. J Mol Biol. 2022;434(14): 167664. - PubMed - DOI
    1. Li DQ, Nair SS, Kumar R. The MORC family: new epigenetic regulators of transcription and DNA damage response. Epigenetics. 2013;8(7):685–93. - PubMed - PMC - DOI
    1. Wang H, Zhang L, Luo Q, Liu J, Wang G. MORC protein family-related signature within human disease and cancer. Cell Death Dis. 2021;12(12):1112. - PubMed - PMC - DOI
    1. Watson ML, Zinn AR, Inoue N, Hess KD, Cobb J, Handel MA, et al. Identification of morc (microrchidia), a mutation that results in arrest of spermatogenesis at an early meiotic stage in the mouse. Proc Natl Acad Sci U S A. 1998;95(24):14361–6. - PubMed - PMC - DOI
    1. Inoue N, Hess KD, Moreadith RW, Richardson LL, Handel MA, Watson ML, et al. New gene family defined by MORC, a nuclear protein required for mouse spermatogenesis. Hum Mol Genet. 1999;8(7):1201–7. - PubMed - DOI

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