Comparative Proteomics Study on Human High-metastatic Large Cell Lung Cancer Cell Lines Before and After Transfecting with nm23-H1 Gene
Background and objective As a tumor metastasis suppressor gene, the functions of nm23-H1 gene are still unclear. The aim of this study is to better understand the mechanism of lung cancer metastasis and to find new biomarkers for early diagnosis and new target for therapy by conducting comparative p...
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Format: | Article |
Language: | zho |
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Chinese Anti-Cancer Association; Chinese Antituberculosis Association
2010-10-01
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Series: | Chinese Journal of Lung Cancer |
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Online Access: | http://www.lungca.org/index.php?journal=01&page=article&op=viewFile&path[]=10.3779%2Fj.issn.1009-3419.2010.10.01&path[]=2090 |
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author | Liwei GAO Wen ZHU Lu LI Mei HOU Li MA Ying ZHAO Qinghua ZHOU |
author_facet | Liwei GAO Wen ZHU Lu LI Mei HOU Li MA Ying ZHAO Qinghua ZHOU |
author_sort | Liwei GAO |
collection | DOAJ |
description | Background and objective As a tumor metastasis suppressor gene, the functions of nm23-H1 gene are still unclear. The aim of this study is to better understand the mechanism of lung cancer metastasis and to find new biomarkers for early diagnosis and new target for therapy by conducting comparative proteomics between the human high-metastatic large cell lung cancer cell lines (L9981) and L9981-nm23-H1 (constructed with transfecting nm23-H1 gene into the L9981 cell line). Methods The total proteins of L9981 and L9981-nm23-H1 were separated by immobilized pH gradient (IPG)-based 2-dimensional electrophoresis (2-DE); the significantly differently expressed proteins were examined by mass spectrometry and analyzed by bioinformatics. Results It was observed that nm23-H1 gene transfection caused remarkable changes of the proteome of L9981 compared with L9981-nm23-H1 cells: 5 proteins were deleted, 9 proteins appeared, 16 proteins downregulated, and 12 proteins up-regulated. These proteins are involved in cell framework, signal transduction, metabolism, proliferation and metastasis. Conclusion After nm23-H1 gene is transfected into L9981, proteome in L9981 is remarkably changed. These changes of the proteome could serve as a basis for reversing the invasive and metastatic phenotype in lung cancer and elucidating the machanisms of the metastasis of lung cancer. |
first_indexed | 2024-12-14T02:07:39Z |
format | Article |
id | doaj.art-0b66b73ecac642b0ae098b30703b6e20 |
institution | Directory Open Access Journal |
issn | 1009-3419 1999-6187 |
language | zho |
last_indexed | 2024-12-14T02:07:39Z |
publishDate | 2010-10-01 |
publisher | Chinese Anti-Cancer Association; Chinese Antituberculosis Association |
record_format | Article |
series | Chinese Journal of Lung Cancer |
spelling | doaj.art-0b66b73ecac642b0ae098b30703b6e202022-12-21T23:20:50ZzhoChinese Anti-Cancer Association; Chinese Antituberculosis AssociationChinese Journal of Lung Cancer1009-34191999-61872010-10-011310928932Comparative Proteomics Study on Human High-metastatic Large Cell Lung Cancer Cell Lines Before and After Transfecting with nm23-H1 GeneLiwei GAOWen ZHULu LIMei HOULi MAYing ZHAOQinghua ZHOUBackground and objective As a tumor metastasis suppressor gene, the functions of nm23-H1 gene are still unclear. The aim of this study is to better understand the mechanism of lung cancer metastasis and to find new biomarkers for early diagnosis and new target for therapy by conducting comparative proteomics between the human high-metastatic large cell lung cancer cell lines (L9981) and L9981-nm23-H1 (constructed with transfecting nm23-H1 gene into the L9981 cell line). Methods The total proteins of L9981 and L9981-nm23-H1 were separated by immobilized pH gradient (IPG)-based 2-dimensional electrophoresis (2-DE); the significantly differently expressed proteins were examined by mass spectrometry and analyzed by bioinformatics. Results It was observed that nm23-H1 gene transfection caused remarkable changes of the proteome of L9981 compared with L9981-nm23-H1 cells: 5 proteins were deleted, 9 proteins appeared, 16 proteins downregulated, and 12 proteins up-regulated. These proteins are involved in cell framework, signal transduction, metabolism, proliferation and metastasis. Conclusion After nm23-H1 gene is transfected into L9981, proteome in L9981 is remarkably changed. These changes of the proteome could serve as a basis for reversing the invasive and metastatic phenotype in lung cancer and elucidating the machanisms of the metastasis of lung cancer.http://www.lungca.org/index.php?journal=01&page=article&op=viewFile&path[]=10.3779%2Fj.issn.1009-3419.2010.10.01&path[]=2090nm23-H1 geneLung neoplasmsTwo dimensional gel electrophoresisMass spectrometry |
spellingShingle | Liwei GAO Wen ZHU Lu LI Mei HOU Li MA Ying ZHAO Qinghua ZHOU Comparative Proteomics Study on Human High-metastatic Large Cell Lung Cancer Cell Lines Before and After Transfecting with nm23-H1 Gene Chinese Journal of Lung Cancer nm23-H1 gene Lung neoplasms Two dimensional gel electrophoresis Mass spectrometry |
title | Comparative Proteomics Study on Human High-metastatic Large Cell Lung Cancer Cell Lines Before and After Transfecting with nm23-H1 Gene |
title_full | Comparative Proteomics Study on Human High-metastatic Large Cell Lung Cancer Cell Lines Before and After Transfecting with nm23-H1 Gene |
title_fullStr | Comparative Proteomics Study on Human High-metastatic Large Cell Lung Cancer Cell Lines Before and After Transfecting with nm23-H1 Gene |
title_full_unstemmed | Comparative Proteomics Study on Human High-metastatic Large Cell Lung Cancer Cell Lines Before and After Transfecting with nm23-H1 Gene |
title_short | Comparative Proteomics Study on Human High-metastatic Large Cell Lung Cancer Cell Lines Before and After Transfecting with nm23-H1 Gene |
title_sort | comparative proteomics study on human high metastatic large cell lung cancer cell lines before and after transfecting with nm23 h1 gene |
topic | nm23-H1 gene Lung neoplasms Two dimensional gel electrophoresis Mass spectrometry |
url | http://www.lungca.org/index.php?journal=01&page=article&op=viewFile&path[]=10.3779%2Fj.issn.1009-3419.2010.10.01&path[]=2090 |
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