小RNA
转染
糖酵解
细胞生长
卵巢癌
荧光素酶
细胞
活力测定
生物
化学
细胞生物学
癌症研究
分子生物学
癌症
内分泌学
生物化学
新陈代谢
基因
遗传学
作者
J. Jessica Yu,Yun-ting An,Meiyan Zou,Xia Li,Xiaoyuan Dong
出处
期刊:Journal of Biomaterials and Tissue Engineering
[American Scientific Publishers]
日期:2021-06-01
卷期号:11 (6): 1078-1083
被引量:1
标识
DOI:10.1166/jbt.2021.2644
摘要
We investigated whether circRAD23B regulates glycolysis and proliferation of ovarian cancer cells by targeting miRNA-519b-3p. circRAD23B expression in ovarian cancer tissues was significantly higher than that in paracancerous tissues, and miRNA-519b-3p expression in ovarian cance tissues was significantly lower than that in paracancerous tissues ( P < 0.05). Transfection sicircRAD23B or miRNA-519b-3p mimics can greatly attenuate cell viability, glucose consumption, lactic acid level, and CyclinD1 protein level ( P < 0.05), and increase p21 protein level ( P < 0.05). Double luciferase reporter experiment confirmed that circRAD23B could function as a miRNA-519b-3p sponge molecule. Co-transfection of si-circRAD23B and anti-miRNA-519b-3p could greatly decrease cell viability, glucose consumption, lactic acid level, and CyclinD1 protein level ( P < 0.05), and increase p21 protein level by comparison with si-circRAD23B+anti-miRNA-NC group ( P < 0.05). Inhibiting circRAD23B expression can, in turn, inhibit glycolysis and the proliferation of ovarian cancer cells by up-regulating miRNA-519b-3p expression.
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