Circular RNA ACTN4 promotes intrahepatic cholangiocarcinoma progression by recruiting YBX1 to initiate FZD7 transcription

JOURNAL OF HEPATOLOGY

卷:76

Article

Chen, Qinjunjie¹  Wang, Haibo¹  Li, Zheng¹  Li, Fengwei^1,2  Liang, Leilei³  Zou, Yiran¹  Shen, Hao⁴  Li, Jun¹  Xia, Yong¹  Cheng, Zhangjun⁵  Yang, Tian⁴  Wang, Kui²  Shen, Feng¹ 

[1] Naval Med Univ, Eastern Hepatobiliary Surg Hosp, Dept Hepat Surg 4, 225 Changhai Rd, Shanghai 200433, Peoples R China

[2] Naval Med Univ, Eastern Hepatobiliary Surg Hosp, Dept Hepat Surg 2, Shanghai, Peoples R China

[3] Chinese Acad Med Sci, Dept Gynecol Oncol, Canc Inst & Hosp, Canc Hosp, Beijing, Peoples R China

[4] Naval Med Univ, Eastern Hepatobiliary Surg Hosp, Dept Hepatobiliary Surg, Shanghai, Peoples R China

[5] Southeast Univ, Zhongda Hosp, Hepatopancreatobiliary Ctr, Sch Med, Nanjing, Peoples R China

关键词: Intrahepatic cholangiocarcinoma;    circACTN4;    YAP1;    FZD7;    Wnt;    Hippo;   

DOI  :  10.1016/j.jhep.2021.08.027

来源: Elsevier

【 摘 要 】

Background & Aims: Intrahepatic cholangiocarcinoma (ICC) is a primary liver cancer with high aggressiveness and extremely poor prognosis. The role of circular RNAs (circRNAs) in ICC carcinogenesis and progression remains to be determined. Methods: CircRNA microarray was performed to screen signifi- cantly upregulated circRNAs in paired ICC and non-tumor tissues. Colony formation, transwell, and xenograft models were used to examine the role of circRNAs in ICC proliferation and metastasis. RNA pulldown, mass spectrometry, chromatin immunoprecipitation, RNA-binding protein immunoprecipitation, chromatin isolation by RNA purification, electrophoretic mobility shift assay, and luciferase reporter assays were used to explore the molecular sponge role of the circRNA (via miRNA binding), and the interaction between circRNA and RNA-binding proteins. Results: Hsa_circ_0050898, which originated from exon 1 to exon 20 of the ACTN4 gene (named circACTN4), was significantly upregulated in ICC. High circACTN4 expression was associated with enhanced tumor proliferation and metastasis in vitro and in vivo, as well as a worse prognosis following ICC resection. In addition, circACTN4 upregulated Yes-associated protein 1 (YAP1) expression by sponging miR-424-5p. More importantly, circACTN4 also recruited Y-box binding protein 1 (YBX1) to stimulate Frizzled-7 (FZD7) transcription. Furthermore, circACTN4 overexpression in ICC cells enhanced the interaction between YAP1 and b-catenin, which are the core components of the Hippo and Wnt signaling pathways, respectively. Conclusions: CircACTN4 was upregulated in ICC and promoted ICC proliferation and metastasis by acting as a molecular sponge of miR-424-5p, as well as by interacting with YBX1 to transcriptionally activate FZD7. These results suggest that circACTN4 is a potential prognostic marker and therapeutic target for ICC. Lay summary: Intrahepatic cholangiocarcinoma is a primary liver cancer associated with aggressiveness and extremely poor prognosis. It is essential for therapeutic development that we uncover relevant pathogenic pathways. Herein, we showed that a circular RNA (circACTN4) was highly expressed in intrahepatic cholangiocarcinoma and was positively associated with tumor growth and metastasis through key developmental signaling pathways. Thus, circACTN4 could be a prognostic biomarker and therapeutic target for intrahepatic cholangiocarcinoma. (C) 2021 The Authors. Published by Elsevier B.V. on behalf of European Association for the Study of the Liver.

【 授权许可】

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