肝细胞癌
小RNA
转移
体内
癌症研究
肿瘤进展
癌症
肿瘤科
癌
原发性肿瘤
医学
内科学
生物
遗传学
生物化学
基因
作者
Jinzhao Ma,Fu Yang,Chuanchuan Zhou,Feng Liu,Ji‐hang Yuan,Fang Wang,Tiantian Wang,Qingguo Xu,Weiping Zhou,Shuhan Sun
出处
期刊:Hepatology
[Wiley]
日期:2016-10-24
卷期号:65 (2): 529-543
被引量:738
摘要
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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