microRNA-454 promotes liver tumor-initiating cell expansion by regulating SOCS6.

Tumor-initiating cells (T-ICs) are involved in the tumorigenesis, progression, drug resistance and recurrence of hepatocellular carcinoma (HCC). However, the underlying mechanism for the propagation of liver T-ICs remains unclear. Herein, we find that miR-454 is upregulated in liver T-ICs and has an important function in liver T-ICs. Functional studies have revealed that knockdown of miR-454 inhibits liver T-IC self-renewal and tumorigenesis. Conversely, forced miR-454 expression promotes liver T-IC self-renewal and tumorigenesis. Mechanistically, we found that miR-454 downregulates SOCS6 expression in liver T-ICs. The correlation between miR-454 and SOCS6 is validated in human HCC tissues. Furthermore, HCC cells that overexpress miR-454 are resistant to sorafenib treatment. Analysis of patient-derived xenografts (PDXs) further demonstrates that miR-454 may predict sorafenib benefits in HCC patients. In conclusion, our findings reveal the crucial role of miR-454 in liver T-IC expansion and sorafenib response. Copyright © 2020 Elsevier Inc. All rights reserved.

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Zhengqing Lei, Xuewu Tang, Anfeng Si, Pinghua Yang, Lihong Wang, Tao Luo, Guangmeng Guo, Qi Zhang, Zhangjun Cheng. microRNA-454 promotes liver tumor-initiating cell expansion by regulating SOCS6. Experimental cell research. 2020 May 01;390(1):111955

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PMID: 32165166

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