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关键微小RNA通过靶向转化生长因子-β诱导的上皮-间质转化调控非小细胞肺癌的发展。

The Key microRNAs Regulated the Development of Non-small Cell Lung Cancer by Targeting TGF-β-induced epithelial-mesenchymal Transition.

作者信息

Chen Gang, Ye Bo

机构信息

Department of General Surgery, Deqing People's Hospital, Huzhou 313200, China.

Department of Thoracic Surgery, Hangzhou Red Cross Hospital, Hangzhou 310003, China.

出版信息

Comb Chem High Throughput Screen. 2019;22(4):238-244. doi: 10.2174/1386207322666190410151945.

Abstract

PURPOSE

Epithelial-to-Mesenchymal Transition (EMT) was reported to play a key role in the development of Non-Small Cell Lung Cancer (NSCLC). The process of EMT is regulated by the changes of miRNAs expression. However, it is still unknown which miRNA changed the most in the process of canceration and whether these changes played a role in tumor development.

METHODS

A total of 36 SCLC patients treated in our hospital between 11th, 2015 and 10th, 2017 were enrolled. The samples of cancer tissues and paracancer tissues of patients were collected and analyzed. Then, the miRNAs in normal lung cells and NSCLC cells were also analyzed. In the presence of TGF-β, we transfected the miRNA mimics or inhibitor into NSCLC cells to investigate the role of the significantly altered miRNAs in cell migration and invasion and in the process of EMT.

RESULTS

MiR-330-3p was significantly up-regulated in NSCLC cell lines and tissues and miRNA- 205 was significantly down-regulated in NSCLC cell lines and NSCLC tissues. Transfected miRNA-205 mimics or miRMA-330-3p inhibitor inhibited the migration and invasion of NCIH1975 cell and restrained TGF-β-induced EMT in NSCLC cells.

CONCLUSION

miRNA-330-3p and miRNA-205 changed the most in the process of canceration in NSCLC. Furthermore, miR-330-3p promoted cell invasion and metastasis in NSCLC probably by promoting EMT and miR-205 could restrain NSCLC likely by suppressing EMT.

摘要

目的

据报道,上皮-间质转化(EMT)在非小细胞肺癌(NSCLC)的发展中起关键作用。EMT过程受miRNA表达变化的调控。然而,仍不清楚哪种miRNA在癌变过程中变化最大,以及这些变化是否在肿瘤发展中起作用。

方法

纳入2015年11月至2017年10月在我院接受治疗的36例SCLC患者。收集并分析患者的癌组织和癌旁组织样本。然后,还分析了正常肺细胞和NSCLC细胞中的miRNA。在存在转化生长因子-β(TGF-β)的情况下,将miRNA模拟物或抑制剂转染到NSCLC细胞中,以研究显著改变的miRNA在细胞迁移、侵袭以及EMT过程中的作用。

结果

MiR-330-3p在NSCLC细胞系和组织中显著上调,而miRNA-205在NSCLC细胞系和NSCLC组织中显著下调。转染miRNA-205模拟物或miRMA-330-3p抑制剂可抑制NCIH1975细胞的迁移和侵袭,并抑制TGF-β诱导的NSCLC细胞中的EMT。

结论

miRNA-330-3p和miRNA-205在NSCLC癌变过程中变化最大。此外,miR-330-3p可能通过促进EMT促进NSCLC细胞的侵袭和转移,而miR-205可能通过抑制EMT抑制NSCLC。

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