miR-424-3p promotes metastasis of hepatocellular carcinoma via targeting the SRF-STAT1/2 axis

被引:4
作者
Feng, Lan [1 ]
Chen, Xi [1 ]
Li, Peiyao [1 ]
Li, Yuanfeng [1 ]
Zhai, Yun [1 ]
Liu, Xinyi [1 ]
Jin, Qian [1 ]
Zhang, Hongxing [1 ,2 ]
Yu, Chaohui [1 ,3 ]
Xing, Baocai [4 ]
Cui, Ying [5 ]
Cao, Pengbo [9 ]
Zhou, Gangqiao [6 ,7 ,8 ,9 ]
机构
[1] Beijing Inst Radiat Med, Natl Ctr Prot Sci Beijing, State Key Lab Prote, Beijing, Peoples R China
[2] Beijing Inst Life, Beijing Proteome Res Ctr, Natl Ctr Prot Sci Beijing, State Key Lab Prote, Beijing, Peoples R China
[3] Zhejiang Univ, Affiliated Hosp 1, Coll Med, Dept Gastroenterol, Hangzhou, Peoples R China
[4] Peking Univ, Canc Hosp & Inst, Key La Carcinogenesis & Translat Res, Dept Hepatopancreatobiliary Surg 1, Beijing, Peoples R China
[5] Guangxi Med Univ, Affiliated Canc Hosp, Nanning, Peoples R China
[6] Nanjing Med Univ, Collaborat Innovat Ctr Personalized Canc Med, Ctr Global Hlth, Sch Publ Hlth, Nanjing, Peoples R China
[7] Anhui Med Univ, Hefei, Peoples R China
[8] Hebei Univ, Baoding, Peoples R China
[9] 7 Taiping Rd, Beijing 100850, Peoples R China
基金
中国国家自然科学基金;
关键词
SERUM RESPONSE FACTOR; TERNARY COMPLEX; INTERFERON-ALPHA; CELL-MIGRATION; TRANSCRIPTION; EXPRESSION; LIVER; IDENTIFICATION; PROLIFERATION; SUPPRESSES;
D O I
10.1093/carcin/bgad037
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although emerging evidence has established the roles of miRNAs in hepatocellular carcinoma (HCC), the global functional implication of miRNAs in this malignancy remains largely uncharacterized. Here, we aim to systematically identify novel miRNAs involved in HCC and clarify the function and mechanism of specific novel candidate miRNA(s) in this malignancy. Through an integrative omics approach, we identified ten HCC-associated functional modules and a collection of candidate miRNAs. Among them, we demonstrated that miR-424-3p, exhibiting strong associations with extracellular matrix (ECM), promotes HCC cells migration and invasion in vitro and facilitates HCC metastasis in vivo. We further demonstrated that SRF is a direct functional target of miR-424-3p, and is required for the oncogenic activity of miR-424-3p. Finally, we found that miR-424-3p reduces the interferon pathway by attenuating the transactivation of SRF on STAT1/2 and IRF9 genes, which in turn enhances the matrix metalloproteinases (MMPs)-mediated ECM remodeling. This study provides comprehensive functional relevance of miRNAs in HCC by an integrative omics analysis, and further clarifies that miR-424-3p in ECM functional module plays an oncogenic role via reducing the SRF-STAT1/2 axis in this malignancy.
引用
收藏
页码:610 / 625
页数:16
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