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Protein Arginine Methyltransferase 1: A Multi-Purpose Player in the Development of Cancer and Metabolic Disease

Overview
Journal Biomolecules
Publisher MDPI
Date 2025 Feb 26
PMID 40001488
Authors
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Abstract

Protein arginine methyltransferase 1 (PRMT1) is the main PRMT family member involved in the formation of monomethylarginine and asymmetric dimethylarginine on its protein substrates. Many protein substrates of PRMT1 are key mediators of cell proliferation and oncogenesis. As such, the function of PRMT1 has been most prominently investigated in the context of cancer development. However, recent in vitro and in vivo studies have highlighted that PRMT1 may also promote metabolic disorders. With the current review, we aim to present an in-depth overview of how PRMT1 influences epigenetic modulation, transcriptional regulation, DNA damage repair, and signal transduction in cancer. Furthermore, we summarize the current knowledge regarding the role of PRMT1 in metabolic reprogramming, lipid metabolism, and glucose metabolism and describe the association of PRMT1 with numerous metabolic pathologies such as obesity, liver disease, and type 2 diabetes. It has become apparent that inhibiting the function of PRMT1 will likely serve as the most beneficial therapeutic approach, since several PRMT1 inhibitors have already been shown to exert positive effects on both cancer and metabolic disease in preclinical settings. However, pharmacological PRMT1 inhibition has not yet been shown to be therapeutically effective in clinical studies.

References
1.
Zhang X, Jiang Y, Zhong C, Ma N, Zhang E, Zhang F . PRMT1 Promoted HCC Growth and Metastasis In Vitro and In Vivo via Activating the STAT3 Signalling Pathway. Cell Physiol Biochem. 2018; 47(4):1643-1654. DOI: 10.1159/000490983. View

2.
Lamming D, Ye L, Katajisto P, Goncalves M, Saitoh M, Stevens D . Rapamycin-induced insulin resistance is mediated by mTORC2 loss and uncoupled from longevity. Science. 2012; 335(6076):1638-43. PMC: 3324089. DOI: 10.1126/science.1215135. View

3.
Yip H, Papa A . Signaling Pathways in Cancer: Therapeutic Targets, Combinatorial Treatments, and New Developments. Cells. 2021; 10(3). PMC: 8002322. DOI: 10.3390/cells10030659. View

4.
Liu J, Bu X, Chu C, Dai X, Asara J, Sicinski P . PRMT1 mediated methylation of cGAS suppresses anti-tumor immunity. Nat Commun. 2023; 14(1):2806. PMC: 10188589. DOI: 10.1038/s41467-023-38443-3. View

5.
Cai J, Pires K, Ferhat M, Chaurasia B, Buffolo M, Smalling R . Autophagy Ablation in Adipocytes Induces Insulin Resistance and Reveals Roles for Lipid Peroxide and Nrf2 Signaling in Adipose-Liver Crosstalk. Cell Rep. 2018; 25(7):1708-1717.e5. PMC: 6802939. DOI: 10.1016/j.celrep.2018.10.040. View