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

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 th...

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Autores principales: Yan, Xu, Lan-Qin, Cao, Long-Yu, Jin, Zhu-Chu, Chen, Gu-Qing, Zeng, Can-E, Tang, Guo-Qing, Li, Chao-Jun, Duan, Fang, Peng, Zhi-Qiang, Xiao, Cui, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3303868/
https://www.ncbi.nlm.nih.gov/pubmed/22500095
http://dx.doi.org/10.1155/2012/510418
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author Yan, Xu
Lan-Qin, Cao
Long-Yu, Jin
Zhu-Chu, Chen
Gu-Qing, Zeng
Can-E, Tang
Guo-Qing, Li
Chao-Jun, Duan
Fang, Peng
Zhi-Qiang, Xiao
Cui, Li
author_facet Yan, Xu
Lan-Qin, Cao
Long-Yu, Jin
Zhu-Chu, Chen
Gu-Qing, Zeng
Can-E, Tang
Guo-Qing, Li
Chao-Jun, Duan
Fang, Peng
Zhi-Qiang, Xiao
Cui, Li
author_sort Yan, Xu
collection PubMed
description 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.
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spelling pubmed-33038682012-04-12 Quantitative Proteomic Study of Human Lung Squamous Carcinoma and Normal Bronchial Epithelial Acquired by Laser Capture Microdissection Yan, Xu Lan-Qin, Cao Long-Yu, Jin Zhu-Chu, Chen Gu-Qing, Zeng Can-E, Tang Guo-Qing, Li Chao-Jun, Duan Fang, Peng Zhi-Qiang, Xiao Cui, Li J Biomed Biotechnol Research Article 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. Hindawi Publishing Corporation 2012 2012-02-28 /pmc/articles/PMC3303868/ /pubmed/22500095 http://dx.doi.org/10.1155/2012/510418 Text en Copyright © 2012 Xu Yan et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yan, Xu
Lan-Qin, Cao
Long-Yu, Jin
Zhu-Chu, Chen
Gu-Qing, Zeng
Can-E, Tang
Guo-Qing, Li
Chao-Jun, Duan
Fang, Peng
Zhi-Qiang, Xiao
Cui, Li
Quantitative Proteomic Study of Human Lung Squamous Carcinoma and Normal Bronchial Epithelial Acquired by Laser Capture Microdissection
title Quantitative Proteomic Study of Human Lung Squamous Carcinoma and Normal Bronchial Epithelial Acquired by Laser Capture Microdissection
title_full Quantitative Proteomic Study of Human Lung Squamous Carcinoma and Normal Bronchial Epithelial Acquired by Laser Capture Microdissection
title_fullStr Quantitative Proteomic Study of Human Lung Squamous Carcinoma and Normal Bronchial Epithelial Acquired by Laser Capture Microdissection
title_full_unstemmed Quantitative Proteomic Study of Human Lung Squamous Carcinoma and Normal Bronchial Epithelial Acquired by Laser Capture Microdissection
title_short Quantitative Proteomic Study of Human Lung Squamous Carcinoma and Normal Bronchial Epithelial Acquired by Laser Capture Microdissection
title_sort quantitative proteomic study of human lung squamous carcinoma and normal bronchial epithelial acquired by laser capture microdissection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3303868/
https://www.ncbi.nlm.nih.gov/pubmed/22500095
http://dx.doi.org/10.1155/2012/510418
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