Wang Yunjiu, Sun Jian, Li Lingxia, Guo Jinhu, Zhang Jue. The mechanism of miR-190 promoting the incidence of hepatocellular carcinoma by regulating the suppressor of cytokine signaling-5J. Journal of New Medicine, 2021, 52(9): 703-708. DOI: 10.3969/j.issn.0253-9802.2021.09.012
Citation: Wang Yunjiu, Sun Jian, Li Lingxia, Guo Jinhu, Zhang Jue. The mechanism of miR-190 promoting the incidence of hepatocellular carcinoma by regulating the suppressor of cytokine signaling-5J. Journal of New Medicine, 2021, 52(9): 703-708. DOI: 10.3969/j.issn.0253-9802.2021.09.012

The mechanism of miR-190 promoting the incidence of hepatocellular carcinoma by regulating the suppressor of cytokine signaling-5

  • Objective To investigate the mechanism of microRNA-190 (miR-190) mediating the incidence of hepatocellular carcinoma (HCC) through regulating the suppressor of cytokine signaling-5 (SOCS5). Methods The liver cancer tissues and adjacent tissues were collected from 84 HCC patients. The expression level of miR-190 was detected by real-time fluorescent quantitative PCR(RT-PCR), and its correlation with clinical characteristics and prognosis of the patients was analyzed. miR-190 mimic/inhibitor or SOCS5 siRNA (siSOCS5) were transfected into the SNU398 and HepG2 cells. Cell proliferation was detected by CCK-8 assay. Cell invasion and migration were detected by Transwell assay. The expression levels of SOCS5 mRNA and protein were determined by RT-PCR and Western blot. The targeted relationship between miR-190 and SOCS5 was verified by dual-luciferase assay. Tumor xenotransplantation was performed to verify the tumor-suppressing effect of SOCS5 in vivo. Results The expression level of miR-190 in HCC was up-regulated, and high expression of miR-190 was associated with tumor size, lymph node metastasis, clinical stage and poor prognosis(all P < 0.05).The results of CCK-8 and Transwell assay showed that over-expression of miR-190 could promote cell proliferation, invasion and migration. RT-PCR, Western blot and dual-luciferase assay confirmed that SOCS5 was the true target of miR-190. In addition, SOCS5 could promote the development of HCC both in vivo and in vitro. Conclusion The miR-190 can promote the incidence and development of HCC by targeting SOCS5, indicating that suppressing miR-190 possesses the potential therapeutic value in restoring the SOCS5 level in HCC.
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