XPD suppresses cell proliferation and migration via miR-29a-3p-Mdm2/PDGF-B axis in HCC

被引:27
作者
Xiao, Zhihua [1 ]
Wang, Yijun [2 ]
Ding, Hao [1 ]
机构
[1] Nanchang Univ, Dept Gastroenterol, Affiliated Hosp 2, 1 Minde Rd, Nanchang 330006, Jiangxi, Peoples R China
[2] Nanchang Univ, Clin Med Coll 2, Nanchang 330006, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
XPD; MiR-29a-3p; Cell proliferation and migration; Hepatocellular carcinoma; HEPATOCELLULAR-CARCINOMA; GROWTH; POLYMORPHISMS; EXPRESSION; INDUCTION; INVASION; PATHWAY; XRCC1; MDM2;
D O I
10.1186/s13578-018-0269-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
ObjectiveThe aim of this study was to investigate the role of XPD in migration and invasion of hepatocellular carcinoma (HCC) cells.MethodsThe expression of XPD and miR-29a-3p was examined by western blot and qRT-PCR, cell proliferation was detected by MTT assay, cell migration was detected by transwell assay. TargetScan was used to predict potential targets of miR-29a-3p.ResultsIn this study, we found that the expression of XPD and miR-29a-3p was downregulated in HCC samples and HCC cell lines. XPD suppressed proliferation and migration of HCC cell via regulating miR-29a-3p expression. Target prediction analysis and dual-luciferase reporter assay confirmed Mdm2 and PDGF-B were direct targets of miR-29a-3p, and miR-29a-3p suppressed proliferation and migration of HCC cells via regulating the expression of Mdm2 or PDGF-B.ConclusionsOur data indicated that XPD suppressed cell proliferation and migration via miR-29a-3p-Mdm2/PDGF-B axis in HCC.
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页数:12
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