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Article type: Research Article
Authors: Du, Zhonghaia | Niu, Shuxianb; * | Xu, Xiaoyuc | Xu, Qinghuib
Affiliations: [a] Cancer Center of Weifang Hospital of Traditional Chinese Medicine, Weifang, Shandong, China | [b] Department of Internal Medicine of Weifang Hospital of Traditional Chinese Medicine, Weifang, Shandong, China | [c] Medical Imaging Center of Weifang Hospital of Traditional Chinese Medicine, Weifang, Shandong, China
Correspondence: [*] Corresponding author: Shuxian Niu, Department of Internal Medicine of Weifang Hospital of Traditional Chinese Medicine, NO. 1055 Weizhou Road, Kuiwen District, Weifang, Shandong, 261041, China. Tel.: +86 536 8060000; E-mail:nsxwftcm2012@163.com
Abstract: BACKGROUNDS: Hepatocellular carcinoma (HCC) is an epithelial cancer that originates from hepatocytes and it is the most common primary malignant tumor of the liver. Till now the prognosis of HCC patients is generally poor. The molecular mechanism giving rise to HCC development and recurrence is still largely unknown. MicroRNA-31 (miR-31) is among the most commonly altered microRNAs in human cancers, and alternations of miR-31 expression were reported to play pivotal roles in tumorigenesis and tumor progression. METHODS: In this work, the primary biological function of miR-31 in HCC tumorigenesis was investigated. RESULTS: Our data showed that overexpression of miR-31 induced markedly inhibition of HCC cell proliferation, migration in vitro and inhibited xenograft tumor growth in vivo. One target gene of miR-31, NDRG3, was also demonstrated indispensable for HCC cell survival. Furthermore, miR-31 and NDRG3 were both essential for HCC cell drug resistance in adriamycin. CONCLUSIONS: We conclude that miR-31 is a crucial regulator in hepatocellular carcinoma, miR-31 and its target gene NDRG3 may be potential therapeutic targets for HCC treatment in the future.
Keywords: Hepatocellular carcinoma, miR-31, NDRG3, tumorigenesis, adriamycin
DOI: 10.3233/CBM-170568
Journal: Cancer Biomarkers, vol. 19, no. 2, pp. 221-230, 2017
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