N6‐methyladenosine demethylase ALKBH5 suppresses colorectal cancer progression potentially by decreasing PHF20 mRNA methylation

• Published in: Clinical and translational medicine 2022-08, Vol.12 (8), p.n/a
• Main Authors: Zhang, Zhen, Wang, Ling, Zhao, Long, Wang, Quan, Yang, Changjiang, Zhang, Mengmeng, Wang, Bo, Jiang, Kewei, Ye, Yingjiang, Wang, Shan, Shen, Zhanlong
• Format: Article
• Language: English
• Subjects: ALKBH5; Antibodies; Cell growth; Clinical medicine; Cloning; Colorectal cancer; Gene expression; m6A modification; Medical prognosis; PHF20; Plasmids; Proteins; Tumors
• ISSN: 2001-1326; 2001-1326
• DOI: 10.1002/ctm2.940

Background As the most widespread mRNAs modification, N6‐methyladenosine (m6A) is dynamically and reversibly modulated by methyltransferases and demethylases. ALKBH5 is a major demethylase, and plays vital roles in the progression of cancers. However, the role and mechanisms of ALKBH5 in colorectal cancer (CRC) is unclear. Results Herein, we discovered that in CRC, downregulated ALKBH5 was closely related to poor prognosis of CRC patients. Functionally, our results demonstrated that knockdown of ALKBH5 enhanced the proliferation, migration and invasion of LOVO and RKO in vitro, while overexpression of ALKBH5 inhibited the functions of these cells. The results also demonstrated that knockdown of ALKBH5 promoted subcutaneous tumorigenesis of LOVO in vivo, while overexpression of ALKBH5 suppressed this ability. Mechanistically, results from joint analyses of MeRIP‐seq and RNA‐seq indicated that PHF20 mRNA was a key molecule that was regulated by ALKBH5‐mediated m6A modification. Further experiments indicated that ALKBH5 may inhibit stability of PHF20 mRNA by removing the m6A modification of PHF20 mRNA 3′UTR. Conclusions ALKBH5 suppresses CRC progression by decreasing PHF20 mRNA methylation. ALKBH5‐mediated m6A modification of PHF20 mRNA can serve as a hopeful strategy for the intervention and treatment of CRC. ALKBH5 expression is down‐regulated in CRC and plays a crucial tumor suppressive role. ALKBH5 inhibits the stability of PHF20 mRNA by removing the m6A modification. Targeting the ALKBH5‐mediated m6A modification of PHF20 mRNA may be a promising therapeutic strategy for intervention and treatment of CRC.