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miR‐320a regulates high mobility group box 1 expression and inhibits invasion and metastasis in hepatocellular carcinoma
Author(s) -
Lv Guixiang,
Wu Mingjuan,
Wang Meijie,
Jiang Xiaochen,
Du Jingli,
Zhang Kaili,
Li Dongliang,
Ma Ning,
Peng Yahui,
Wang Lujing,
Zhou Lingyun,
Zhao Weiming,
Jiao Yufei,
Gao Xu,
Hu Zheng
Publication year - 2017
Publication title -
liver international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.873
H-Index - 110
eISSN - 1478-3231
pISSN - 1478-3223
DOI - 10.1111/liv.13424
Subject(s) - metastasis , hepatocellular carcinoma , cancer research , medicine , ectopic expression , cell , apoptosis , biology , cell culture , cancer , biochemistry , genetics
Background & Aims Several studies have shown that miR‐320a induces apoptosis, inhibits cell proliferation, and affects cell cycle progression as a tumour suppressor in many cancers. However, the involvement of miR‐320a in the invasion and metastasis of hepatocellular carcinoma ( HCC ) is still unknown. Methods Endogenous miR‐320a and high mobility group box 1 ( HMGB 1) expressions were assayed by real‐time PCR . Luciferase activities were measured using a dual‐luciferase reporter assay system. Western blots were used to determine the protein expressions of HMGB 1, MMP 2, and MMP 9. Invasion and metastasis of tumour cells were, respectively, evaluated by the transwell invasion assay and the wound healing assay. Results The expression of miR‐320a was significantly decreased in 24 of 32 (75%) HCC tissues and associated with the invasion and metastasis of HCC . Furthermore, we demonstrated that HMGB 1 was a direct target of miR‐320a and there was a significant negative correlation between miR‐320a and HMGB 1 expression in HCC . Ectopic expression or inhibition of miR‐320a potently regulated the invasion and metastasis of HCC cells in HMGB 1‐dependent manner. Conclusions Our results showed that miR‐320a was involved in the invasion and metastasis by targeting HMGB 1 and had an anti‐metastasis effect in HCC .