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miR-493-5p的高表达通过靶向癌基因ITGB1与非小细胞肺癌的临床预后呈正相关。

High expression of miR-493-5p positively correlates with clinical prognosis of non small cell lung cancer by targeting oncogene ITGB1.

作者信息

Liang Zhu, Kong Rui, He Zhan, Lin Li-Yao, Qin Shan-Shan, Chen Chun-Yuan, Xie Zhan-Qiang, Yu Fei, Sun Guo-Qian, Li Chun-Guang, Fu Da, Jiang Geng-Xi, Chen Jie, Ma Yu-Shui

机构信息

Department of Cardiothoracic Surgery, The Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China.

Medical College of Soochow University, Soochow 215006, China.

出版信息

Oncotarget. 2017 Jul 18;8(29):47389-47399. doi: 10.18632/oncotarget.17650.

Abstract

Increasing evidence supports that microRNA (miRNA)-mediated gene regulation plays a significant functional role in cancer progression. To investigate the expression and clinical significance of ITGB1 in non small cell lung cancer (NSCLC), the expression levels of ITGB1 in NSCLC tissues and human normal lung tissues were analyzed in silico using genes microarray, KEGG pathway and hierarchical clustering analysis followed by validation with quantitative RT-PCR. Our results showed that ITGB1 was upregulated in NSCLC tissues when compared with normal lung tissues. Survival analysis based on the qRT-PCR data established that ITGB1 expression was attentively related to the prognosis of NSCLC, and patients with higher ITGB1 expression had shorter overall survival (OS). Moreover, ITGB1 was confirmed to be a direct target of miR-493-5p. Furthermore, concomitant high expression of ITGB1 and low expression of miR-493-5p correlated with a shorter median OS and PFS in NSCLC patients. In conclusion, our results provide the first evidence that ITGB1 is a direct target of miR-493-5p suggesting that ITGB1 and miR-493-5p may have potential prognostic value and may be useful as tumor biomarkers for the diagnosis of NSCLC patients.

摘要

越来越多的证据支持,微小RNA(miRNA)介导的基因调控在癌症进展中发挥着重要的功能作用。为了研究整合素β1(ITGB1)在非小细胞肺癌(NSCLC)中的表达及临床意义,我们利用基因芯片、KEGG通路和层次聚类分析在计算机上分析了NSCLC组织和人正常肺组织中ITGB1的表达水平,随后通过定量逆转录聚合酶链反应(qRT-PCR)进行验证。我们的结果显示,与正常肺组织相比,ITGB1在NSCLC组织中上调。基于qRT-PCR数据的生存分析表明,ITGB1表达与NSCLC的预后密切相关,ITGB1表达较高的患者总生存期(OS)较短。此外,ITGB1被证实是miR-493-5p的直接靶点。此外,ITGB1高表达和miR-493-5p低表达同时出现与NSCLC患者较短的中位OS和无进展生存期(PFS)相关。总之,我们的结果首次证明ITGB1是miR-493-5p的直接靶点,提示ITGB1和miR-493-5p可能具有潜在的预后价值,并且可能作为NSCLC患者诊断的肿瘤生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446a/5564573/becb3e95fd6f/oncotarget-08-47389-g001.jpg

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