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非小细胞肺癌血清标志物PACAP的蛋白质组学筛选和鉴定

BACKGROUND AND OBJECTIVE: Early diagnosis and treatment of lung cancer contribute to a patient's prolonged survival. Proteomics and tissue culture were used to screen potential serum markers of lung cancer. METHODS: The differential proteomic technique and matrix-assisted laser desorption/ioniz...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000130/
https://www.ncbi.nlm.nih.gov/pubmed/22613335
http://dx.doi.org/10.3779/j.issn.1009-3419.2012.05.07
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collection PubMed
description BACKGROUND AND OBJECTIVE: Early diagnosis and treatment of lung cancer contribute to a patient's prolonged survival. Proteomics and tissue culture were used to screen potential serum markers of lung cancer. METHODS: The differential proteomic technique and matrix-assisted laser desorption/ionization-time of flight mass spectrometry were used to identify overexpressed proteins from cultured tumor tissues in a conditioned medium. Paired lung tissues in a conditioned medium were used as the control group. Overexpressed proapoptotic caspase adaptor protein (PACAP) was identified using Western blot and enzyme-linked immunosorbent assay (ELISA). RESULTS: The expression of nineteen protein spots exhibited a twofold increase compared with that in the control group. Fourteen of which were identified, including the distinctly overexpressed PACAP. Western blot analysis revealed a high level of PACAP in the lung adenocarcinoma in both tissue culture media and patients' serum. Overexpressed PACAP was also detected in the serum of non-small cell lung cancer patients via ELISA compared with that in the serum of small cell lung cancer patients, benign lung tumor patients, and healthy individuals (P < 0.05). CONCLUSION: PACAP is a potential serum marker of non-small cell lung cancer.
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spelling pubmed-60001302018-07-06 非小细胞肺癌血清标志物PACAP的蛋白质组学筛选和鉴定 Zhongguo Fei Ai Za Zhi 临床研究 BACKGROUND AND OBJECTIVE: Early diagnosis and treatment of lung cancer contribute to a patient's prolonged survival. Proteomics and tissue culture were used to screen potential serum markers of lung cancer. METHODS: The differential proteomic technique and matrix-assisted laser desorption/ionization-time of flight mass spectrometry were used to identify overexpressed proteins from cultured tumor tissues in a conditioned medium. Paired lung tissues in a conditioned medium were used as the control group. Overexpressed proapoptotic caspase adaptor protein (PACAP) was identified using Western blot and enzyme-linked immunosorbent assay (ELISA). RESULTS: The expression of nineteen protein spots exhibited a twofold increase compared with that in the control group. Fourteen of which were identified, including the distinctly overexpressed PACAP. Western blot analysis revealed a high level of PACAP in the lung adenocarcinoma in both tissue culture media and patients' serum. Overexpressed PACAP was also detected in the serum of non-small cell lung cancer patients via ELISA compared with that in the serum of small cell lung cancer patients, benign lung tumor patients, and healthy individuals (P < 0.05). CONCLUSION: PACAP is a potential serum marker of non-small cell lung cancer. 中国肺癌杂志编辑部 2012-05-20 /pmc/articles/PMC6000130/ /pubmed/22613335 http://dx.doi.org/10.3779/j.issn.1009-3419.2012.05.07 Text en 版权所有©《中国肺癌杂志》编辑部2012 https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/
spellingShingle 临床研究
非小细胞肺癌血清标志物PACAP的蛋白质组学筛选和鉴定
title 非小细胞肺癌血清标志物PACAP的蛋白质组学筛选和鉴定
title_full 非小细胞肺癌血清标志物PACAP的蛋白质组学筛选和鉴定
title_fullStr 非小细胞肺癌血清标志物PACAP的蛋白质组学筛选和鉴定
title_full_unstemmed 非小细胞肺癌血清标志物PACAP的蛋白质组学筛选和鉴定
title_short 非小细胞肺癌血清标志物PACAP的蛋白质组学筛选和鉴定
title_sort 非小细胞肺癌血清标志物pacap的蛋白质组学筛选和鉴定
topic 临床研究
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000130/
https://www.ncbi.nlm.nih.gov/pubmed/22613335
http://dx.doi.org/10.3779/j.issn.1009-3419.2012.05.07
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