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地塞米松对顺铂诱导中国人肺腺癌原代细胞凋亡的影响

BACKGROUND AND OBJECTIVE: Glucocorticoids, such as dexamethasone (DEX), have been widely used in conjunction with cancer therapy due to inducing apoptosis in lymphoid cells and preventing nausea and vomiting. However, recent research indicates induction of therapy-resistance by glucocorticoids in lu...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000686/
https://www.ncbi.nlm.nih.gov/pubmed/20672700
http://dx.doi.org/10.3779/j.issn.1009-3419.2010.01.05
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description BACKGROUND AND OBJECTIVE: Glucocorticoids, such as dexamethasone (DEX), have been widely used in conjunction with cancer therapy due to inducing apoptosis in lymphoid cells and preventing nausea and vomiting. However, recent research indicates induction of therapy-resistance by glucocorticoids in lung cancer in European, although it is unclear whether DEX mediates the resistance of cisplatin-induced apoptosis in primary cells from resected Chinese human lung adenocarcinoma specimens. METHODS: Ten primary cells from resected Chinese human lung adenocarcinoma specimens were treated with cisplatin in the presence or absence of DEX. The number of viable and dead cells was evaluated by trypan blue exclusion; the cell proliferation was measured by the MTT-assay; the cell apoptotic rate was analyzed by flow cytometry. RESULTS: In this study, it was found that DEX reduced the effect of cisplatin-induced proliferation inhibition in all of the primary cells from 10 examined tumor samples. On the other hand, the cell death and apoptosis induced by cisplatin in human lung adenocarcinoma cells line A549 could also be inhibited in the presence of DEX during 2 and 3 weeks' co-incubation. CONCLUSION: DEX may reduce the effect of chemotherapy with cisplatin, and it urges carefully reconsideration of the application of DEX in treatment of patients with lung adenocarcinoma in China.
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spelling pubmed-60006862018-07-06 地塞米松对顺铂诱导中国人肺腺癌原代细胞凋亡的影响 Zhongguo Fei Ai Za Zhi 基础研究 BACKGROUND AND OBJECTIVE: Glucocorticoids, such as dexamethasone (DEX), have been widely used in conjunction with cancer therapy due to inducing apoptosis in lymphoid cells and preventing nausea and vomiting. However, recent research indicates induction of therapy-resistance by glucocorticoids in lung cancer in European, although it is unclear whether DEX mediates the resistance of cisplatin-induced apoptosis in primary cells from resected Chinese human lung adenocarcinoma specimens. METHODS: Ten primary cells from resected Chinese human lung adenocarcinoma specimens were treated with cisplatin in the presence or absence of DEX. The number of viable and dead cells was evaluated by trypan blue exclusion; the cell proliferation was measured by the MTT-assay; the cell apoptotic rate was analyzed by flow cytometry. RESULTS: In this study, it was found that DEX reduced the effect of cisplatin-induced proliferation inhibition in all of the primary cells from 10 examined tumor samples. On the other hand, the cell death and apoptosis induced by cisplatin in human lung adenocarcinoma cells line A549 could also be inhibited in the presence of DEX during 2 and 3 weeks' co-incubation. CONCLUSION: DEX may reduce the effect of chemotherapy with cisplatin, and it urges carefully reconsideration of the application of DEX in treatment of patients with lung adenocarcinoma in China. 中国肺癌杂志编辑部 2010-01-20 /pmc/articles/PMC6000686/ /pubmed/20672700 http://dx.doi.org/10.3779/j.issn.1009-3419.2010.01.05 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
地塞米松对顺铂诱导中国人肺腺癌原代细胞凋亡的影响
title 地塞米松对顺铂诱导中国人肺腺癌原代细胞凋亡的影响
title_full 地塞米松对顺铂诱导中国人肺腺癌原代细胞凋亡的影响
title_fullStr 地塞米松对顺铂诱导中国人肺腺癌原代细胞凋亡的影响
title_full_unstemmed 地塞米松对顺铂诱导中国人肺腺癌原代细胞凋亡的影响
title_short 地塞米松对顺铂诱导中国人肺腺癌原代细胞凋亡的影响
title_sort 地塞米松对顺铂诱导中国人肺腺癌原代细胞凋亡的影响
topic 基础研究
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000686/
https://www.ncbi.nlm.nih.gov/pubmed/20672700
http://dx.doi.org/10.3779/j.issn.1009-3419.2010.01.05
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