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首页> 外文期刊>EBioMedicine >Synaptotagmin 7 in twist-related protein 1-mediated epithelial – Mesenchymal transition of non-small cell lung cancer
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Synaptotagmin 7 in twist-related protein 1-mediated epithelial – Mesenchymal transition of non-small cell lung cancer

机译:突触相关蛋白1介导的上皮-非小细胞肺癌间质转化中的突触结合蛋白7

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Background Twist-related protein 1 (TWIST1) plays an essential role in the carcinogenesis and metastasis of NSCLC. Our aims were to identify the molecule at the downstream of TWIST1 and to evaluate its potential as a diagnostic and a prognostic marker in NSCLC. Methods The functional genes at the downstream of TWIST1 were obtained via microarray gene expression analyses in the NSCLC cell line. The expression levels of synaptotagmin 7 (SYT7) in a cohort of patients with NSCLC ( n =?154) were examined using immunohistochemistry staining and assessed by Kaplan-Meier survival analysis and Cox regression analysis. The effects of SYT7 on the tumorigenesis and metastasis of NSCLC were measured in NSCLC cells. In vivo xenograft lung cancer models were used to study the tumorigenesis role of SYT7. Findings We discovered that SYT7 is significantly altered by TWIST1 expression. We further confirmed that SYT7 protein was significantly higher in NSCLC than that in the adjacent normal lung tissue, and higher SYT7 expression was associated with poor survival of NSCLC patients. The protein level of SYT7 was positively correlated with TWIST1 in NSCLC tissue. Functional experiments indicated that SYT7 promoted proliferation, invasion, and metastasis and inhibited cell apoptosis of NSCLC cells in vitro. In vivo experiments showed that sh SYT7 inhibited the xenograft tumor growth of NSCLC cells. Knocking down of SYT7 increased the expression of E-cadherin and decreased the level of N-cadherin and Vimentin in cultured cells. Interpretation Our data indicate that SYT7 is an important promoter for EMT and tumor progression in NSCLC. Fund This project was supported by grants from the Major Scientific and Technological Innovation Project of Shandong Province (2018CXGC1212), Science and Technology Foundation of Shandong Province (2014GSF118084, 2016GSF121043), Medical and Health Technology Innovation Plan of Jinan City (201805002) and the National Natural Science Foundation of China (81372333).
机译:背景扭曲相关蛋白1(TWIST1)在NSCLC的癌变和转移中起着至关重要的作用。我们的目的是鉴定TWIST1下游的分子,并评估其在NSCLC中作为诊断和预后标志物的潜力。方法通过微阵列基因在NSCLC细胞系中的表达分析,获得TWIST1下游的功能基因。使用免疫组织化学染色检查了一组NSCLC患者(n =?154)中突触结合蛋白7(SYT7)的表达水平,并通过Kaplan-Meier生存分析和Cox回归分析进行了评估。在NSCLC细胞中测量SYT7对NSCLC的肿瘤发生和转移的影响。体内异种移植肺癌模型用于研究SYT7的肿瘤发生作用。结果我们发现TWIST1表达明显改变了SYT7。我们进一步证实,NSCLC中的SYT7蛋白显着高于相邻的正常肺组织,而SYT7的高表达与NSCLC患者的不良生存有关。 NSCLC组织中SYT7蛋白水平与TWIST1正相关。功能实验表明,SYT7在体外能促进NSCLC细胞的增殖,侵袭和转移,并抑制其凋亡。体内实验表明,sh SYT7抑制了NSCLC细胞的异种移植肿瘤生长。敲除SYT7可增加培养细胞中E-钙粘蛋白的表达,并降低N-钙粘蛋白和波形蛋白的水平。解释我们的数据表明,SYT7是NSCLC中EMT和肿瘤进展的重要启动子。基金该项目获得了山东省重大科技创新项目(2018CXGC1212),山东省科学技术基金会(2014GSF118084、2016GSF121043),济南市医疗卫生技术创新计划(201805002)和国家科学基金的资助。中国自然科学基金(81372333)。

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