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西妥昔单抗对非小细胞肺癌细胞的体外抑制作用
BACKGROUND AND OBJECTIVE: The epidermal growth factor receptor (EGFR) monoclonal antibody cetuximab has been used widely in non-small cell lung cancer patients. The aim of this study is to explore the effect of lung cancer cells (A549, H460, H1299, SPC-A-1) which were treated by cetuximab in vitro....
Formato: | Online Artículo Texto |
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Lenguaje: | English |
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中国肺癌杂志编辑部
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000554/ https://www.ncbi.nlm.nih.gov/pubmed/20704815 http://dx.doi.org/10.3779/j.issn.1009-3419.2010.08.03 |
_version_ | 1783331766400974848 |
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collection | PubMed |
description | BACKGROUND AND OBJECTIVE: The epidermal growth factor receptor (EGFR) monoclonal antibody cetuximab has been used widely in non-small cell lung cancer patients. The aim of this study is to explore the effect of lung cancer cells (A549, H460, H1299, SPC-A-1) which were treated by cetuximab in vitro. METHODS: We studied the effects of increasing concentrations of cetuximab (1 nmol/L-625 nmol/L) in four human lung cancer cell lines (A549, SPC-A-1, H460, H1229). CCK8 measured the inhibition of cell proliferation in each group. A549, SPC-A-1 were marked by PI and the statuses of apoptosis were observed. Western blot were used to detect the proliferation-related signaling protein and apoptosis-related protein in A549. RESULTS: The treatment with cetuximab resulted in the effect on cell proliferation and apoptosis in a time- and dosedependent manner. The expression of activated key enzymes (p-AKT, p-EGFR, p-MAPK) in EGFR signaling transduction pathway were down-regulated more obviously. CONCLUSION: Cetuximab is an effective targeted drug in the treatment of lung cancer cell lines, tissues, most likely to contribute to the inhibition of key enzymes in EGFR signaling transduction pathway. |
format | Online Article Text |
id | pubmed-6000554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | 中国肺癌杂志编辑部 |
record_format | MEDLINE/PubMed |
spelling | pubmed-60005542018-07-06 西妥昔单抗对非小细胞肺癌细胞的体外抑制作用 Zhongguo Fei Ai Za Zhi 基础研究 BACKGROUND AND OBJECTIVE: The epidermal growth factor receptor (EGFR) monoclonal antibody cetuximab has been used widely in non-small cell lung cancer patients. The aim of this study is to explore the effect of lung cancer cells (A549, H460, H1299, SPC-A-1) which were treated by cetuximab in vitro. METHODS: We studied the effects of increasing concentrations of cetuximab (1 nmol/L-625 nmol/L) in four human lung cancer cell lines (A549, SPC-A-1, H460, H1229). CCK8 measured the inhibition of cell proliferation in each group. A549, SPC-A-1 were marked by PI and the statuses of apoptosis were observed. Western blot were used to detect the proliferation-related signaling protein and apoptosis-related protein in A549. RESULTS: The treatment with cetuximab resulted in the effect on cell proliferation and apoptosis in a time- and dosedependent manner. The expression of activated key enzymes (p-AKT, p-EGFR, p-MAPK) in EGFR signaling transduction pathway were down-regulated more obviously. CONCLUSION: Cetuximab is an effective targeted drug in the treatment of lung cancer cell lines, tissues, most likely to contribute to the inhibition of key enzymes in EGFR signaling transduction pathway. 中国肺癌杂志编辑部 2010-08-20 /pmc/articles/PMC6000554/ /pubmed/20704815 http://dx.doi.org/10.3779/j.issn.1009-3419.2010.08.03 Text en 版权所有©《中国肺癌杂志》编辑部2010 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 | 基础研究 西妥昔单抗对非小细胞肺癌细胞的体外抑制作用 |
title | 西妥昔单抗对非小细胞肺癌细胞的体外抑制作用 |
title_full | 西妥昔单抗对非小细胞肺癌细胞的体外抑制作用 |
title_fullStr | 西妥昔单抗对非小细胞肺癌细胞的体外抑制作用 |
title_full_unstemmed | 西妥昔单抗对非小细胞肺癌细胞的体外抑制作用 |
title_short | 西妥昔单抗对非小细胞肺癌细胞的体外抑制作用 |
title_sort | 西妥昔单抗对非小细胞肺癌细胞的体外抑制作用 |
topic | 基础研究 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000554/ https://www.ncbi.nlm.nih.gov/pubmed/20704815 http://dx.doi.org/10.3779/j.issn.1009-3419.2010.08.03 |
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