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miR-125a-5p inhibits tumorigenesis in hepatocellular carcinoma
Author(s) -
Xin Xu,
Yuquan Tao,
Yongjie Niu,
Zhixian Wang,
Congcong Zhang,
Yongchun Yu,
Lifang Ma
Publication year - 2019
Publication title -
aging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.473
H-Index - 90
ISSN - 1945-4589
DOI - 10.18632/aging.102276
Subject(s) - carcinogenesis , cancer research , hepatocellular carcinoma , apoptosis , gene knockdown , cell growth , in vivo , mapk/erk pathway , cell , suppressor , biology , signal transduction , medicine , cancer , microbiology and biotechnology , biochemistry , genetics
Hepatocellular carcinoma (HCC) is one of the most prevalent and deadly cancers world-wide. miR-125a-5p is a tumor suppressor in HCC and other cancers, but its mechanisms of action during HCC tumorigenesis remain largely unknown. In this study, we found that miR-125a-5p expression was significantly lower in HCC tissues and cell lines than matched normal tissues and liver cells. miR-125a-5p overexpression inhibited HCC cell proliferation and induced apoptosis in vitro and in vivo , while miR-125a-5p knockdown had the opposite effects. In addition, PTPN1 and MAP3K11 were identified as targets of miR-125a-5p. Knocking down PTPN1 and MAP3K11 activated the JNK MAPK signaling pathway to suppress HCC cell proliferation and induce apoptosis. Our findings suggest that miR-125a-5p may be a useful therapeutic target for treatment of HCC patients.

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