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miR-193b的失调通过转化生长因子-β和SMAD3信号通路的调控影响结肠癌细胞的生长。

Deregulation of miR-193b affects the growth of colon cancer cells via transforming growth factor-β and regulation of the SMAD3 pathway.

作者信息

Wu Kaiming, Zhao Zhenxian, Ma Jun, Chen Jianhui, Peng Jianjun, Yang Shibin, He Yulong

机构信息

Department of Gastrointestinal Surgery, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong 510080, P.R. China.

Department of Pancreato-Biliary Surgery, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong 510080, P.R. China.

出版信息

Oncol Lett. 2017 Apr;13(4):2557-2562. doi: 10.3892/ol.2017.5763. Epub 2017 Feb 22.

Abstract

MicroRNA-193b (miRNA-193b) is often differentially expressed and is an important regulator of gene expression in colon cancer. The aim of the present study was to determine whether miRNA-193b affects cell growth in colon cancer and to investigate the potential underlying mechanisms. Patients with colorectal cancer (CRC; n=20) and healthy volunteers (n=10) were enrolled from the Department of Gastrointestinal Surgery Center, First Affiliated Hospital of Sun Yat-Sen University (Guangzhou, China). Western blot analysis was used to evaluate the protein expression of SMAD3 and transforming growth factor-β (TGF-β) in the patient samples. It was determined that miRNA-193b expression was markedly elevated in the CRC tissue samples. Furthermore, silencing of miRNA-193bin SW620 CRC cells by specific inhibitors significantly reduced the cell proliferation and induced apoptosis. In addition, the downregulation of miRNA-193b significantly activated the protein expression of SMAD3 and TGF-β, and promoted caspase-3 activity in SW620 cells. The results of the present study suggested that the deregulation of miRNA-193b may affect cell growth in colon cancer via the TGF-β and SMAD3 signaling pathways.

摘要

微小RNA-193b(miRNA-193b)常常存在差异表达,是结肠癌中基因表达的重要调节因子。本研究旨在确定miRNA-193b是否影响结肠癌细胞的生长,并探究其潜在的作用机制。研究对象来自中山大学附属第一医院胃肠外科中心(中国广州),纳入了20例结直肠癌(CRC)患者和10例健康志愿者。采用蛋白质印迹分析评估患者样本中SMAD3和转化生长因子-β(TGF-β)的蛋白表达。结果显示,CRC组织样本中miRNA-193b的表达显著升高。此外,用特异性抑制剂沉默SW620 CRC细胞中的miRNA-193b可显著降低细胞增殖并诱导细胞凋亡。另外,miRNA-193b的下调显著激活了SW620细胞中SMAD3和TGF-β的蛋白表达,并促进了caspase-3的活性。本研究结果表明,miRNA-193b的失调可能通过TGF-β和SMAD3信号通路影响结肠癌细胞的生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1b0/5403328/f3cbb6c30d88/ol-13-04-2557-g00.jpg

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