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

被引:0
|
作者
de Korte, Daphne [1 ]
Hoekstra, Menno [1 ]
机构
[1] Leiden Univ, Leiden Acad Ctr Drug Res, Div Syst Pharmacol & Pharm, Gorlaeus Labs, Einsteinweg 55, NL-2333 CC Leiden, Netherlands
关键词
PRMT1; protein arginine methyltransferase; cancer; metabolism; type; 2; diabetes; obesity; liver disease; FOXO TRANSCRIPTION FACTORS; INSULIN-RESISTANCE; DIABETES-MELLITUS; PRMT1; PROMOTES; HISTONE H4; IN-VIVO; METHYLATION; REVEALS; LIVER; MICRORNAS;
D O I
10.3390/biom15020185
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
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页数:21
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