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微小RNA-382通过靶向LMO3抑制非小细胞肺癌中的癌细胞生长和转移。

MicroRNA-382 inhibits cancer cell growth and metastasis in NSCLC via targeting LMO3.

作者信息

Chen Dingzhu, Zhang Yi, Lin Yong, Shen Feimin, Zhang Zhijian, Zhou Jiguang

机构信息

Department of Cardiac and Thoracic Surgery, Zhangzhou Hospital Affiliated to Fujian Medical University, Zhangzhou, Fujian 363000, P.R. China.

Department of Clinical Laboratory, Zhangzhou Hospital Affiliated to Fujian Medical University, Zhangzhou, Fujian 363000, P.R. China.

出版信息

Exp Ther Med. 2019 Apr;17(4):2417-2424. doi: 10.3892/etm.2019.7271. Epub 2019 Feb 13.

Abstract

Recent studies have revealed a pivotal role of microRNAs (miRs) in regulating the initiation and development of multiple types of cancer. In the present study, it was discovered that miR-382 may be an important tumor suppressor in non-small cell lung cancer (NSCLC). It was demonstrated that miR-382 expression was downregulated in tumor tissues from patients with NSCLC compared with adjacent normal tissues. Furthermore, overexpression of miR-382 suppressed cell proliferation and cell migration of NSCLC cells. In addition, reverse transcription-quantitative polymerase chain reaction and the luciferase reporter assay revealed that LIM-only protein 3 (LMO3), an oncogene, acted as a direct target gene of miR-382. Notably, overexpression of miR-382 did not alter cell proliferation or migration in LMO3-silenced A549 cells. Furthermore, analysis of patient tissues indicated an elevation of LMO3 expression in tumor tissues compared with adjacent normal tissues and a negative association between miR-382 and LMO3 mRNA expression levels. Taken together, the present findings indicated that miR-382 inhibited NSCLC cell proliferation and metastasis by targeting LMO3, suggesting a tumor suppressor role of miR-382 in NSCLC.

摘要

近期研究揭示了微小RNA(miR)在调控多种癌症的发生和发展过程中发挥着关键作用。在本研究中,发现miR-382可能是非小细胞肺癌(NSCLC)中的一种重要肿瘤抑制因子。结果表明,与邻近正常组织相比,NSCLC患者肿瘤组织中miR-382表达下调。此外,miR-382的过表达抑制了NSCLC细胞的增殖和迁移。另外,逆转录定量聚合酶链反应和荧光素酶报告基因检测显示,原癌基因单LIM结构域蛋白3(LMO3)是miR-382的直接靶基因。值得注意的是,在LMO3沉默的A549细胞中,miR-382的过表达并未改变细胞增殖或迁移。此外,对患者组织的分析表明,与邻近正常组织相比,肿瘤组织中LMO3表达升高,且miR-382与LMO3 mRNA表达水平呈负相关。综上所述,本研究结果表明,miR-382通过靶向LMO3抑制NSCLC细胞增殖和转移,提示miR-382在NSCLC中具有肿瘤抑制作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8e9/6425134/cba462b5d121/etm-17-04-2417-g00.jpg

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