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Identification of Candidate Biomarkers for Early Detection of Human Lung Squamous Cell Cancer by Quantitative Proteomics

机译:定量蛋白质组学鉴定可早期检测人肺鳞状细胞癌的候选生物标志物

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摘要

To discover novel biomarkers for early detection of human lung squamous cell cancer (LSCC) and explore possible mechanisms of LSCC carcinogenesis, iTRAQ-tagging combined with two dimensional liquid chromatography tandem MS analysis was used to identify differentially expressed proteins in human bronchial epithelial carcinogenic process using laser capture microdissection-purified normal bronchial epithelium (NBE), squamous metaplasia (SM), atypical hyper-plasia (AH), carcinoma in situ (CIS) and invasive LSCC. As a result, 102 differentially expressed proteins were identified, and three differential proteins (GSTP1, HSPB1 and CKB) showing progressively expressional changes in the carcinogenic process were selectively validated by Western blotting. Immunohistochemistry was performed to detect the expression of the three proteins in an independent set of paraffin-embedded archival specimens including various stage tissues of bronchial epithelial carcinogenesis, and their ability for early detection of LSCC was evaluated by receiver operating characteristic analysis. The results showed that the combination of the three proteins could perfectly discriminate NBE from preneoplastic lesions (SM, AH and CIS) from invasive LSCC, achieving a sensitivity of 96% and a specificity of 92% in discriminating NBE from preneoplatic lesions, a sensitivity of 100% and a specificity of 98% in discriminating NBE from invasive LSCC, and a sensitivity of 92% and a specificity of 91 % in discriminating preneoplatic lesions from invasive LSCC, respectively. Furthermore, we knocked down GSTP1 in immortalized human bronchial epithelial cell line 16HBE cells, and then measured their susceptibility to carcinogen benzo(a)pyrene-induced cell transformation. The results showed that GSTP1 knockdown significantly increased the efficiency of benzo(a)pyrene-induced 16HBE cell transformation. The present data first time show that GSTP1, HSPB1 and CKB are novel potential biomarkers for early detection of LSCC, and GSTP1 down-regulation is involved in human bronchial epithelial carcinogenesis.
机译:为了发现用于早期检测人肺鳞状细胞癌(LSCC)的新型生物标记物并探索LSCC癌变的可能机制,使用iTRAQ-tag结合二维液相色谱串联MS分析来鉴定人支气管上皮致癌过程中差异表达的蛋白质。激光捕获显微切割纯化的正常支气管上皮(NBE),鳞状化生(SM),非典型增生(AH),原位癌(CIS)和浸润性LSCC。结果,鉴定了102种差异表达的蛋白质,并且通过Western印迹法选择性地验证了三种在致癌过程中表现出逐渐表达变化的差异蛋白质(GSTP1,HSPB1和CKB)。进行了免疫组织化学检测,在独立的一组石蜡包埋的档案标本中(包括支气管上皮癌变的各个阶段组织)检测了这三种蛋白质的表达,并通过接受者操作特征分析评估了它们早期检测LSCC的能力。结果表明,这三种蛋白质的组合可以完美地区分NBE和浸润性LSCC的肿瘤前病变(SM,AH和CIS),敏感性为96%,特异性为92%,区分NBE与新陈旧性病变。区分NBE和浸润性LSCC的特异性分别为100%和98%,区分浸润性LSCC的新板前病变的敏感性分别为92%和91%。此外,我们敲低了永生化的人支气管上皮细胞系16HBE细胞中的GSTP1,然后测量了它们对致癌物苯并(a)-诱导的细胞转化的敏感性。结果表明,GSTP1敲低显着提高了苯并(a)re诱导的16HBE细胞转化的效率。首次本数据表明,GSTP1,HSPB1和CKB是用于LSCC早期检测的新型潜在生物标记,并且GSTP1下调与人支气管上皮癌变有关。

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