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

被引:58
|
作者
Zeng, Gu-Qing [1 ,2 ]
Zhang, Pang-Fei [1 ]
Deng, Xingming [4 ,5 ]
Yu, Feng-Lei [3 ]
Li, Cui [1 ]
Xu, Yan [1 ]
Yi, Hong [1 ]
Li, Mao-Yu [1 ]
Hu, Rong [1 ]
Zuo, Jian-Hong [1 ]
Li, Xin-Hui [1 ]
Wan, Xun-Xun [1 ]
Qu, Jia-Quan [1 ]
He, Qiu-Yan [1 ]
Li, Jian-Huang [1 ]
Ye, Xu [1 ]
Chen, Yu [1 ]
Li, Jiao-Yang [1 ]
Xiao, Zhi-Qiang [1 ]
机构
[1] Cent S Univ, Xiangya Hosp, Key Lab Canc Prote, Chinese Minist Hlth, Changsha 410008, Hunan, Peoples R China
[2] Univ S China, Sch Med, Dept Gen Surg & Operat Surg, Hengyang 421001, Peoples R China
[3] Cent S Univ, Dept Cardiothorac Surg, Xiangya Hosp 2, Changsha 410011, Hunan, Peoples R China
[4] Emory Univ, Sch Med, Dept Radiat Oncol, Atlanta, GA 30322 USA
[5] Emory Univ, Winship Canc Inst, Atlanta, GA 30322 USA
关键词
LASER CAPTURE MICRODISSECTION; GLUTATHIONE-S-TRANSFERASE; MULTIDIMENSIONAL LIQUID-CHROMATOGRAPHY; TANDEM MASS-SPECTROMETRY; HEAT-SHOCK PROTEINS; CREATINE-KINASE BB; NASOPHARYNGEAL CARCINOMA; EXPRESSION; SERUM; HSP27;
D O I
10.1074/mcp.M111.013946
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
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 hyperplasia (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. Molecular & Cellular Proteomics 11: 10.1074/mcp.M111.013946, 1-16, 2012.
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页数:16
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