Quantitative Proteomic Study of Human Lung Squamous Carcinoma and Normal Bronchial Epithelial Acquired by Laser Capture Microdissection

Author:

Yan Xu12,Lan-Qin Cao3,Long-Yu Jin4,Zhu-Chu Chen1,Gu-Qing Zeng5,Can-E Tang1,Guo-Qing Li6,Chao-Jun Duan1,Fang Peng1,Zhi-Qiang Xiao1,Cui Li1

Affiliation:

1. Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University, Changsha 410008, China

2. Judicial Police General Hospital, Changsha 410004, China

3. Department of Gynecology and Obstetrics, Xiangya Hospital, Central South University, Changsha 410008, China

4. Department of Cardiothoracic Surgery, Third Xiangya Hospital, Central South University, Changsha 410013, China

5. Department of General Introduction to Surgery, School of Medicine, University of South China, Hengyang 421001, China

6. Department of Biology, School of Pharmacy and Life Science, University of South China, Hengyang 421001, China

Abstract

Objective. To investigate the differential protein profile of human lung squamous carcinoma (HLSC) and normal bronchial epithelium (NBE) and provide preliminary results for further study to explore the carcinogenic mechanism of HLSC.Methods. Laser capture microdissection (LCM) was used to purify the target cells from 10 pairs of HLSC tissues and their matched NHBE, respectively. A stable-isotope labeled strategy using iTRAQ, followed by 2D-LC/Q-STAR mass spectrometry, was performed to separate and identify the differential expression proteins.Results. A total of 96 differential expression proteins in the LCM-purified HLSC and NBE were identified. Compared with NBE, 49 proteins were upregulated and 47 proteins were downregulated in HLSC. Furthermore, the expression levels of the differential proteins including HSPB1, CKB, SCCA1, S100A8, as well as S100A9 were confirmed by western blot and tissue microarray and were consistent with the results of quantitative proteomics.Conclusion. The different expression proteins in HLSC will provide scientific foundation for further study to explore the carcinogenic mechanism of HLSC.

Funder

National Natural Science Foundation of China

Publisher

Hindawi Limited

Subject

Health, Toxicology and Mutagenesis,Genetics,Molecular Biology,Molecular Medicine,General Medicine,Biotechnology

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