Circular RNA TGFBR2 acts as a ceRNA to suppress nasopharyngeal carcinoma progression by sponging miR-107

鼻咽癌 竞争性内源性RNA 小RNA 下调和上调 生物 癌症研究 微阵列分析技术 肿瘤进展 微阵列 核糖核酸 长非编码RNA 基因表达调控 环状RNA 基因表达 癌症 医学 基因 内科学 放射治疗 遗传学
作者
Wanpeng Li,Hanyu Lu,Huan Wang,Xianhui Ning,Quan Liu,Huankang Zhang,Zhuofu Liu,Jingjing Wang,Weidong Zhao,Yurong Gu,Houyong Li,Xicai Sun,Li Hu,Dehui Wang
出处
期刊:Cancer Letters [Elsevier BV]
卷期号:499: 301-313 被引量:44
标识
DOI:10.1016/j.canlet.2020.11.001
摘要

Circular RNAs (circRNAs) act as competing endogenous RNAs, which are involved in the regulation of many types of cancers. They primarily function by sponging microRNAs (miRNAs) and influencing the expression of miRNA by target messenger RNA. However, the role of circRNAs in the progression of nasopharyngeal carcinoma (NPC) remains largely unclear. In this study, differentially expressed miRNAs associated with NPC were screened using microarray analyses, from which miR-107 was identified. Increased miR-107 expression was associated with poor prognosis in NPC, and miR-107 promoted the proliferation and migration of NPC cells. TGFBR2 was identified as the direct target of miR-107, which could reverse its effect on NPC cells. Furthermore, the expression of circTGFBR2 was downregulated in NPC tissue samples, while circTGFBR2 overexpression correlated with favorable prognosis in NPC. Functionally, circTGFBR2 overexpression inhibited the proliferation and migration of NPC cells both in vitro and in vivo. Further analysis showed that circTGFBR2 sponged miR-107, leading to the upregulation of TGFBR2 expression and suppression of NPC progression. Therefore, circTGFBR2 may serve as a novel tumor suppressive factor and potential target for new therapies in NPC patients.
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