Zeng Zhenguo, Yang Yuting, Qing Cheng, Hu Zhiguo, Huang Yiming, Zhou Chaoqi, Li Dan, Jiang Yanxia
Department of Critical Care Medicine, The First Affiliated Hospital of Nanchang University.
Department of Critical Care Medicine, Inner Mongolia People's Hospital, Hohhot, Inner Mongolia.
Medicine (Baltimore). 2020 Mar;99(10):e19451. doi: 10.1097/MD.0000000000019451.
Non-small cell lung cancer (NSCLC) is the major cause of cancer mortality worldwide. Though multidisciplinary therapies have been widely used for NSCLC, its overall prognosis remains very poor, presumably owing to lack of effective prognostic biomarkers. SMAD, a well-known transcription factor, plays an essential role in carcinogenesis. Aberrant expression of SMAD have been found in various cancers, and may be regarded as prognostic indicator for some malignancies. However, the expression and prognostic role of SMAD family member, especially at the mRNA level, remain elusive in NSCLC. In the present study, we report the distinct expression and prognostic value of individual SMAD in patients with NSCLC by analyzing several online databases including ONCOMINE, Gene Expression Profiling Interactive Analysis, Human Protein Atlas database, Kaplan-Meier plotter, cBioPortal, and Database for Annotation, Visualization and Integrated Discovery. The mRNA levels of SMAD6/7/9 in NSCLC were significantly down-regulated in NSCLC, and aberrant SMAD2/3/4/5/6/7/9 mRNA levels were all correlated with the prognosis of NSCLC. Collectively, SMAD2/3/4/5/6/7/9 may server as prognostic biomarkers and potential targets for NSCLC, and thus facilitate the customized treatment strategies for NSCLC patients.
非小细胞肺癌(NSCLC)是全球癌症死亡的主要原因。尽管多学科治疗已广泛应用于NSCLC,但由于缺乏有效的预后生物标志物,其总体预后仍然很差。SMAD是一种著名的转录因子,在致癌过程中起重要作用。SMAD的异常表达已在各种癌症中发现,可能被视为某些恶性肿瘤的预后指标。然而,SMAD家族成员的表达及其预后作用,尤其是在mRNA水平上,在NSCLC中仍不清楚。在本研究中,我们通过分析多个在线数据库,包括ONCOMINE、基因表达谱交互式分析、人类蛋白质图谱数据库、Kaplan-Meier绘图仪、cBioPortal以及注释、可视化和综合发现数据库,报告了NSCLC患者中单个SMAD的不同表达及其预后价值。NSCLC中SMAD6/7/9的mRNA水平显著下调,并且SMAD2/3/4/5/6/7/9的异常mRNA水平均与NSCLC的预后相关。总体而言,SMAD2/3/4/5/6/7/9可能作为NSCLC的预后生物标志物和潜在靶点,从而有助于为NSCLC患者制定个性化的治疗策略。