METTL14 suppresses the metastatic potential of hepatocellular carcinoma by modulating N6-methyladenosine-dependent primary MicroRNA processing
Jin-zhao Ma, Fu Yang, Chuan-chuan Zhou, Feng Liu, Ji-hang Yuan, Fang Wang, Tian-tian Wang, Qing-guo Xu, Wei-ping Zhou, Shu-han Sun
Journal:HEPATOLOGY
IF:11.71
DOI:10.1002/hep.28885
PMID:27774652
Published:2016-10-24
research field:肿瘤学分子生物学癌症遗传学
Abstract
N 6 -Methyladenosine (m 6 A) modification has been implicated in many biological processes. However, its role in cancer has not been well studied. Here, we demonstrate that m 6 A modifications are decreased in hepatocellular carcinoma, especially in metastatic hepatocellular carcinoma, and that methyltransferase-like 14 (METTL14) is the main factor involved in aberrant m 6 A modification. Moreover, METTL14 down-regulation acts as an adverse prognosis factor for recurrence-free survival of hepatocellular carcinoma and is significantly associated with tumor metastasis in vitro and in vivo . We confirm that METTL14 interacts with the microprocessor protein DGCR8 and positively modulates the primary microRNA 126 process in an m 6 A-dependent manner. Further experiments show that microRNA 126 inhibits the repressing effect of METTL14 in tumor metastasis. Conclusion : These studies reveal an important role of METTL14 in tumor metastasis and provide a fresh view on m 6 A modification in tumor progression. (H epatology 2017;65:529-543).
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