4.7 Review

Targeting protein arginine methyltransferase 5 in cancers: Roles, inhibitors and mechanisms

Journal

BIOMEDICINE & PHARMACOTHERAPY
Volume 144, Issue -, Pages -

Publisher

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2021.112252

Keywords

PRMT5; Cancer; Inhibitors; Histone methylation

Funding

  1. National Natural Science Foundation of China [82000074]
  2. Scientific Research Funding Project of Education Department of Liaoning Province [jyt-dldxjc202005]
  3. Doctoral Start-up Foundation of Liaoning Province [2021-BS-282]
  4. Science and Technol-ogy Innovation Fund Project of Dalian [2020JJ27SN071]
  5. Dalian Youth Science and Technology Star Research Project [2020RQ080]

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PRMT5 functions as a crucial player in various cancers and has emerged as a promising target in cancer epigenetic therapy. There are existing PRMT5 inhibitors with different molecular mechanisms, but current issues need to be addressed to facilitate the future discovery of PRMT5 targeted drugs for cancer treatment.
The protein arginine methyltransferase 5 (PRMT5) as the major type II arginine methyltransferase catalyzes the monoand symmetric dimethylation of arginine residues in both histone and non-histone proteins. Recently, increasing evidence has demonstrated that PRMT5 plays an indispensable role in the occurrence and development of various human cancers by promoting the cell proliferation, invasion, and migration. It has become a promising and valuable target in the cancer epigenetic therapy. This review is to summarize the clinical significance of PRMT5 in the cancers such as lung cancer, breast cancer and colorectal cancer, and the drug discovery targeting PRMT5. Importantly, the existing PRMT5 inhibitors representing different molecular mechanisms, and their pharmacological effect, mechanism of action and biological affinity are analyzed. Clinical status, current problems and future perspective of PRMT5 inhibitors for the treatment of cancers are also discussed, all of which provides crucial help for the future discovery of PRMT5 targeted drugs for cancer treatment.

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