PKA-dependent growth stimulation of cells derived from human pulmonary adenocarcinoma and small airway epithelium by dexamethasone

被引:13
作者
Al-Wadei, HAN
Takahasi, T
Schuller, HM
机构
[1] Univ Tennessee, Coll Vet Med, Dept Pathobiol, Knoxville, TN 37996 USA
[2] Univ Tennessee, Coll Vet Med, Expt Oncol Lab, Knoxville, TN USA
[3] Nagoya Univ, Grad Sch Med, Ctr Neurol Dis, Dept Mol Carcinogenesis, Nagoya, Aichi, Japan
关键词
lung adenocarcinoma; dexamethasone; cAMP; PKA; CREB; ERK1/2; cell proliferation;
D O I
10.1016/j.ejca.2005.09.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Smoking is a risk factor for lung cancer, chronic obstructive pulmonary disease, chronic bronchitis and asthma. The chronic lung diseases are also a predisposing factor for the development of lung cancer. Glucocorticoids are used for the management of chronic lung diseases because of their anti-inflammatory activity. These drugs also have anti-tumourigenic effects in mouse models of lung cancer. Glucocorticoids are frequently used as co-treatment with cancer therapy. Using the human pulmonary adenocarcinoma (PAC) cell line NCI-H322 with features of bronchiolar Clara cells, and immortalised human small airway epithelial cells, our data show that the glucocorticoid dexamethasone increased cell proliferation in MTT assays in a PKA-dependent manner. Dexamethasone significantly increased intracellular cAMP in direct immunoassays. Immunoblot analysis revealed increased phosphorylation of ERK1/2 and of the transcription factor CREB in response to dexamethasone. These data suggest that glucocorticoids could have tumour promoting activity on a sub-set of human PAC. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2745 / 2753
页数:9
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