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Start Over Author "Feng, Xuping" Publisher springer science and business media llc
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2. Correction: CircNFIB inhibits tumor growth and metastasis through suppressing MEK1/ERK signaling in intrahepatic cholangiocarcinoma

Author

Du, Jinpeng, primary, Lan, Tian, additional, Liao, Haotian, additional, Feng, Xuping, additional, Chen, Xing, additional, Liao, Wenwei, additional, Hou, Guimin, additional, Xu, Lin, additional, Feng, Qingbo, additional, Xie, Kunlin, additional, Liao, Mingheng, additional, Chen, Xiangzheng, additional, Huang, Jiwei, additional, Yuan, Kefei, additional, and Zeng, Yong, additional

Published
2023
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7. CircNFIB inhibits tumor growth and metastasis through suppressing MEK1/ERK signaling in intrahepatic cholangiocarcinoma

Author

Du, Jinpeng, Lan, Tian, Liao, Haotian, Feng, Xuping, Chen, Xing, Liao, Wenwei, Hou, Guimin, Xu, Lin, Feng, Qingbo, Xie, Kunlin, Liao, Mingheng, Chen, Xiangzheng, Huang, Jiwei, Yuan, Kefei, and Zeng, Yong

Subjects
Adult, Male, Cancer Research, MAP Kinase Signaling System, Metastasis, Cholangiocarcinoma, Mice, Trametinib, Cell Line, Tumor, Biomarkers, Tumor, Animals, Humans, Neoplasm Metastasis, Intrahepatic cholangiocarcinoma (ICC), Circular RNA, RC254-282, Aged, Neoplasm Staging, Research, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RNA, Circular, Middle Aged, Prognosis, Xenograft Model Antitumor Assays, Gene Expression Regulation, Neoplastic, Disease Models, Animal, NFI Transcription Factors, Bile Duct Neoplasms, Dual specificity mitogen-activated protein kinase kinase 1 (MEK1), Oncology, Molecular Medicine, Female, Disease Susceptibility
Abstract

Background Considerable evidence shows that circular RNAs (circRNAs) play an important role in tumor development. However, their function in intrahepatic cholangiocarcinoma (ICC) metastasis and the underlying mechanisms are incompletely understood. Methods circNFIB (hsa_circ_0086376, termed as cNFIB hereafter) was identified in human ICC tissues through circRNAs sequencing. The biological role of cNFIB was determined in vitro and in vivo by gain or loss of functional experiments. Fluorescence in situ hybridization (FISH), RNA immunoprecipitation (RIP) and RNA pull-down assays were conducted to analyze the interaction of cNFIB with dual specificity mitogen-activated protein kinase kinase1 (MEK1). Duolink in situ proximity ligation assay (PLA) and coimmunoprecipitation (co-IP) assay were used to investigate the effects of cNFIB on the interaction between MEK1 and mitogen-activated protein kinase 2 (ERK2). Finally, a series of in vitro and in vivo experiments were performed to explore the influences of cNFIB on the anti-tumor activity of trametinib (a MEK inhibitor). Results cNFIB was significantly down-regulated in human ICC tissues with postoperative metastases. The loss of cNFIB was highly associated with aggressive characteristics and predicted unfavorable prognosis in ICC patients. Functional studies revealed that cNFIB inhibited the proliferation and metastasis of ICC cells in vitro and in vivo. Mechanistically, cNFIB competitively interacted with MEK1, which induced the dissociation between MEK1 and ERK2, thereby resulting in the suppression of ERK signaling and tumor metastasis. Moreover, we found that ICC cells with high levels of cNFIB held the potential to delay the trametinib resistance. Consistently, in vivo and in vitro studies demonstrated that cotreatment with trametinib and lentivirus vector encoding cNFIB showed greater inhibitory effect than isolated trametinib treatment. Conclusions Our findings identified that cNFIB played a key role in ICC growth and metastasis by regulating MEK1/ERK signaling. Given the efficacy of cNFIB modulation on ICC suppression and trametinib sensitivity, cNFIB appears to be a potential therapeutic molecule for ICC treatment.

Published
2022

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