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Early Candidate Biomarkers of Non–Small Cell Lung Cancer Are Screened and Identified in Premalignant Lung Lesions

机译:非小细胞肺癌的早期候选生物标志物在恶性肺病变中的筛选和鉴定

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A specific protein profile that accompanies neoplastic transformation in the premalignant airway epithelium could provide an opportunity for early diagnosis of lung cancer. The aim of this study was to screen and identify early candidate biomarkers of non–small cell lung cancer. Thirteen non–small cell lung cancer samples were obtained within 30 minutes after a surgical resection. Laser capture microdissection was performed to enrich the normal lung cell and squamous metaplasia or atypical adenomatous hyperplasia cell populations. The resulting tandem mass spectrum was automatically searched for proteins against International Protein Index (IPI) human protein database using the TurboSEQUEST searching engine. The molecular function and biological processes of identified proteins were determined based on universal bioinformatics tools. The 2 proteins of interest, focal adhesion kinase and C-terminal Src kinase, were validated using Western blot method. A total of 863 proteins were identified by automatically searching the tandem mass spectrum, among which 427 were dysregulated expression in premalignant airway epithelium compared with those of normal lung cells. The 427 proteins were mainly distributed in 24 sorts of cellular components, 22 molecular function, 15 biological processes, and 10 significant perturbations of pathways. The most significant network included 48 genes and was related to energy production, cell cytoskeleton, cell adhesion, metabolism, oxidative stress, and small molecule biochemistry. Focal adhesion kinase and C-terminal Src kinase were significantly overexpressed in premalignant lung lesion cells compared with the normal lung cells in 13 cases. We identified that there were 427 proteins involved in non–small cell lung cancer carcinogenic process and confirmed the key biological pathways in premalignant lung tissue. The significantly upregulated focal adhesion kinase and C-terminal Src kinase could be considered as molecular biomarkers for early diagnosis and prognosis of non–small cell lung cancer.
机译:恶变前气道上皮中伴随肿瘤转化的特定蛋白质谱可能为肺癌的早期诊断提供机会。这项研究的目的是筛选和鉴定非小细胞肺癌的早期候选生物标志物。手术切除后30分钟内获得了13个非小细胞肺癌样本。进行激光捕获显微切割以富集正常肺细胞和鳞状化生或非典型腺瘤性增生细胞群。使用TurboSEQUEST搜索引擎,针对国际蛋白质索引(IPI)人蛋白质数据库自动搜索所得的串联质谱。鉴定的蛋白质的分子功能和生物学过程是基于通用生物信息学工具确定的。使用蛋白质印迹法验证了感兴趣的2种蛋白质,即粘着斑激酶和C端Src激酶。通过自动搜索串联质谱,共鉴定出863种蛋白质,其中427种与正常肺细胞相比在恶性气道上皮中表达失调。 427种蛋白质主要分布在24种细胞成分,22种分子功能,15种生物学过程和10种途径的显着扰动中。最重要的网络包括48个基因,与能量产生,细胞骨架,细胞粘附,代谢,氧化应激和小分子生物化学有关。与正常肺细胞相比,在13例恶变前肺病变细胞中灶性黏附激酶和C末端Src激酶明显过量表达。我们确定非小细胞肺癌致癌过程中涉及427种蛋白质,并证实了癌前肺组织中的关键生物学途径。粘着斑激酶和C末端Src激酶的显着上调可以被认为是非小细胞肺癌早期诊断和预后的分子生物标志物。

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