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sCD40L联合长春瑞滨对肺腺癌A549细胞的作用
BACKGROUND AND OBJECTIVE: The results of published data on the effect of CD40 signal related to cancer cell sensitivity to chemotherapy are inconclusive. The aim of this study is to investigate the effect of soluble CD40 ligand (sCD40L) combined with vinorelbine on lung adenocarcinoma cell line A549...
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/PMC6000372/ https://www.ncbi.nlm.nih.gov/pubmed/20673484 http://dx.doi.org/10.3779/j.issn.1009-3419.2010.07.06 |
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collection | PubMed |
description | BACKGROUND AND OBJECTIVE: The results of published data on the effect of CD40 signal related to cancer cell sensitivity to chemotherapy are inconclusive. The aim of this study is to investigate the effect of soluble CD40 ligand (sCD40L) combined with vinorelbine on lung adenocarcinoma cell line A549. METHODS: Lung adenocarcinoma A549 cells were chosen as target cells and CD40 signal was stimulated by sCD40L. MTT assay and flow cytometry were used to determine the changes of cell proliferation, cell cycle and apoptosis of A549 cells treated by vinorelbine after CD40 was stimulated. The activity of Caspase-3 was measured using Caspase-3 cellular activity assay kit plus. RESULTS: After CD40 stimulation, an increase of inhibition on CD40 positive cell line A549 proliferation was confirmed when vinorelbine was added (P < 0.05). However, no significant changes were shown in apoptosis and cell cycle (P > 0.05). On the other hand, the activity of Caspase-3 was substantially decreased (P < 0.05). CONCLUSION: Stimulation of CD40 can increase lung adenocarcinoma cell line A549 sensitivity to vinorelbine, which may be through a non-apoptosis, Caspase independent mechanism, and not associated with the inhibition of cell cycle. |
format | Online Article Text |
id | pubmed-6000372 |
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-60003722018-07-06 sCD40L联合长春瑞滨对肺腺癌A549细胞的作用 Zhongguo Fei Ai Za Zhi 基础研究 BACKGROUND AND OBJECTIVE: The results of published data on the effect of CD40 signal related to cancer cell sensitivity to chemotherapy are inconclusive. The aim of this study is to investigate the effect of soluble CD40 ligand (sCD40L) combined with vinorelbine on lung adenocarcinoma cell line A549. METHODS: Lung adenocarcinoma A549 cells were chosen as target cells and CD40 signal was stimulated by sCD40L. MTT assay and flow cytometry were used to determine the changes of cell proliferation, cell cycle and apoptosis of A549 cells treated by vinorelbine after CD40 was stimulated. The activity of Caspase-3 was measured using Caspase-3 cellular activity assay kit plus. RESULTS: After CD40 stimulation, an increase of inhibition on CD40 positive cell line A549 proliferation was confirmed when vinorelbine was added (P < 0.05). However, no significant changes were shown in apoptosis and cell cycle (P > 0.05). On the other hand, the activity of Caspase-3 was substantially decreased (P < 0.05). CONCLUSION: Stimulation of CD40 can increase lung adenocarcinoma cell line A549 sensitivity to vinorelbine, which may be through a non-apoptosis, Caspase independent mechanism, and not associated with the inhibition of cell cycle. 中国肺癌杂志编辑部 2010-07-20 /pmc/articles/PMC6000372/ /pubmed/20673484 http://dx.doi.org/10.3779/j.issn.1009-3419.2010.07.06 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 sCD40L联合长春瑞滨对肺腺癌A549细胞的作用 |
title | sCD40L联合长春瑞滨对肺腺癌A549细胞的作用 |
title_full | sCD40L联合长春瑞滨对肺腺癌A549细胞的作用 |
title_fullStr | sCD40L联合长春瑞滨对肺腺癌A549细胞的作用 |
title_full_unstemmed | sCD40L联合长春瑞滨对肺腺癌A549细胞的作用 |
title_short | sCD40L联合长春瑞滨对肺腺癌A549细胞的作用 |
title_sort | scd40l联合长春瑞滨对肺腺癌a549细胞的作用 |
topic | 基础研究 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000372/ https://www.ncbi.nlm.nih.gov/pubmed/20673484 http://dx.doi.org/10.3779/j.issn.1009-3419.2010.07.06 |
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