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AnnexinA7 promotes epithelial–mesenchymal transition by interacting with Sorcin and contributes to aggressiveness in hepatocellular carcinoma

Fei Ling, Huan Zhang, Yunliang Sun, Jinyi Meng, Jaceline Gislaine Pires Sanches, He Huang, Qingqing Zhang, Xiao Yu, Bo Wang, Li Hou, Jun Zhang

2021Cell Death and Disease15 citationsDOIOpen Access PDF

Abstract

Hepatocellular carcinoma (HCC) is one of the most common cancers worldwide, and metastasis is the major cause of the high mortality of HCC. In this study, we identified that AnnexinA7 (ANXA7) and Sorcin (SRI) are overexpressed and interacting proteins in HCC tissues and cells. In vitro functional investigations revealed that the interaction between ANXA7 and SRI regulated epithelial-mesenchymal transition (EMT), and then affected migration, invasion, and proliferation in HCC cells. Furthermore overexpression/knockdown of ANXA7 was remarkably effective in promoting/inhibiting tumorigenicity and EMT in vivo. Altogether, our study unveiled a mechanism that ANXA7 promotes EMT by interacting with SRI and further contributes to the aggressiveness in HCC, which provides a novel potential therapeutic target for preventing recurrence and metastasis in HCC.

Topics & Concepts

Hepatocellular carcinomaGene knockdownEpithelial–mesenchymal transitionMetastasisCancer researchIn vivoMesenchymal stem cellIn vitroMechanism (biology)MedicineBiologyChemistryCell cultureCancerPathologyInternal medicineBiochemistryEpistemologyPhilosophyBiotechnologyGeneticsWnt/β-catenin signaling in development and cancerAxon Guidance and Neuronal SignalingS100 Proteins and Annexins
AnnexinA7 promotes epithelial–mesenchymal transition by interacting with Sorcin and contributes to aggressiveness in hepatocellular carcinoma | Litcius