Feng Xiaocheng, Dong Xuehong, Wu Dingting, Zhao Hanxin, Xu Changqin, Li Hong
Department of Endocrinology and Metabolism, Zhejiang University Affiliated Sir Run Shaw Hospital, School of Medicine, Hangzhou, P.R. China.
Department of Nutrition Division, Zhejiang University Affiliated Fourth Hospital, School of Medicine, Yiwu, P.R. China.
Histol Histopathol. 2020 Feb;35(2):217-224. doi: 10.14670/HH-18-155. Epub 2019 Jul 29.
Emerging evidence has shown that long noncoding RNA (lncRNA) plays an important role in various types of malignant cancer. Small nucleolar RNA host gene 12 (SNHG12) was found to be upregulated and to act as an oncogene in several cancers. However, the function and regulatory mechanism of SNHG12 remain unclear in papillary thyroid carcinoma (PTC). In this study, SNHG12 was found to be increased in PTC tissues and cell lines using quantitative real-time PCR. Knockdown of SNHG12 significantly inhibited PTC cell proliferation, migration and invasion and induced apoptosis in vitro. Mechanistic investigations revealed that SNHG12 functions as a competing endogenous RNA (ceRNA) to sponge miR-16-5p, which was downregulated in PTC tissues. In addition, rescue assays further confirmed that SNHG12 contributed to the progression of PTC through regulating miR-16-5p expression. These results indicated that SNHG12 might contribute to tumor progression in PTC by acting as a ceRNA to sponge miR-16-5p.
新出现的证据表明,长链非编码RNA(lncRNA)在各种类型的恶性肿瘤中发挥着重要作用。小核仁RNA宿主基因12(SNHG12)在几种癌症中被发现上调并作为癌基因发挥作用。然而,SNHG12在甲状腺乳头状癌(PTC)中的功能和调控机制仍不清楚。在本研究中,通过定量实时PCR发现SNHG12在PTC组织和细胞系中表达增加。敲低SNHG12可显著抑制PTC细胞的增殖、迁移和侵袭,并在体外诱导细胞凋亡。机制研究表明,SNHG12作为竞争性内源RNA(ceRNA)发挥作用,吸附PTC组织中表达下调的miR-16-5p。此外,挽救实验进一步证实SNHG12通过调节miR-16-5p的表达促进PTC的进展。这些结果表明,SNHG12可能通过作为ceRNA吸附miR-16-5p来促进PTC的肿瘤进展。