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微小RNA-3613-5p通过RELA和AKT/MAPK正反馈环促进肺腺癌细胞增殖。

MicroRNA-3613-5p Promotes Lung Adenocarcinoma Cell Proliferation through a RELA and AKT/MAPK Positive Feedback Loop.

作者信息

He Tao, Shen Hongyou, Wang Shuangmiao, Wang Yanfang, He Zhiwei, Zhu Litong, Du Xinyue, Wang Dan, Li Jiao, Zhong Shizhen, Huang Wenhua, Yang Huiling

机构信息

Department of Biology, School of Basic Medical Sciences, Guangdong Medical University, Dongguan, Guangdong 523808, P.R. China.

Emergency Department, Cancer Center, Integrated Hospital of Traditional Chinese Medicine, Southern Medical University, Guangzhou, Guangdong 510310, P.R. China.

出版信息

Mol Ther Nucleic Acids. 2020 Sep 26;22:572-583. doi: 10.1016/j.omtn.2020.09.024. eCollection 2020 Dec 4.

Abstract

Aberrant activation of nuclear factor κB (NF-κB)/RELA is often found in lung adenocarcinoma (LUAD). In this study, we determined that microRNA-3613-5p (miR-3613-5p) plays a crucial role in RELA-mediated post-transcriptional regulation of LUAD cell proliferation. Expression of miR-3613-5p in clinical LUAD specimens is associated with poor prognosis in LUAD. Upregulation of miR-3613-5p promotes LUAD cell proliferation and . Our results suggested a mechanism whereby miR-3613-5p expression is induced by RELA through its direct interaction with JUN, thereby stimulating the AKT/mitogen-activated protein kinase (MAPK) pathway by directly targeting NR5A2. In addition, we also found that phosphorylation of AKT1 and MAPK3/1 co-transactivates RELA, thus constituting a RELA/JUN/miR-3613-5p/NR5A2/AKT1/MAPK3/1 positive feedback loop, leading to persistent NF-κB activation. Our findings also revealed that miR-3613-5p plays an oncogenic role in LUAD by promoting cell proliferation and acting as a key regulator of the positive feedback loop underlying the link between the NF-κB/RELA and AKT/MAPK pathways.

摘要

核因子κB(NF-κB)/RELA的异常激活在肺腺癌(LUAD)中经常被发现。在本研究中,我们确定微小RNA-3613-5p(miR-3613-5p)在RELA介导的LUAD细胞增殖的转录后调控中起关键作用。miR-3613-5p在临床LUAD标本中的表达与LUAD的不良预后相关。miR-3613-5p的上调促进LUAD细胞增殖。我们的结果提示了一种机制,即RELA通过与JUN直接相互作用诱导miR-3613-5p表达,从而通过直接靶向NR5A2刺激AKT/丝裂原活化蛋白激酶(MAPK)途径。此外,我们还发现AKT1和MAPK3/1的磷酸化共同反式激活RELA,从而构成一个RELA/JUN/miR-3613-5p/NR5A2/AKT1/MAPK3/1正反馈环,导致NF-κB的持续激活。我们的研究结果还表明,miR-3613-5p通过促进细胞增殖并作为NF-κB/RELA与AKT/MAPK途径之间联系的正反馈环的关键调节因子,在LUAD中发挥致癌作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aae5/7562961/8827e65892cf/fx1.jpg

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