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The mechanisms and significance of up-regulation of RhoB expression by hypoxia and glucocorticoid in rat lung and A549 cells.
- Source :
-
Journal of cellular and molecular medicine [J Cell Mol Med] 2016 Jul; Vol. 20 (7), pp. 1276-86. Date of Electronic Publication: 2016 Feb 24. - Publication Year :
- 2016
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Abstract
- Small guanosine triphosphate (GTP)-binding protein RhoB is an important stress sensor and contributes to the regulation of cytoskeletal organization, cell proliferation and survival. However, whether RhoB is involved in the hypoxic response and action of glucocorticoid (GC) is largely unknown. In this study, we investigated the effects of hypoxia or/and GC on the expression and activition of RhoB in the lung of rats and human A549 lung carcinoma cells, and further studied its mechanism and significance. We found that hypoxia and dexamethasone (Dex), a synethic GC, not only significantly increased the expression and activation of RhoB independently but also coregulated the expresion of RhoB in vitro and in vivo. Up-regulation of RhoB by hypoxia was in part through stabilizing the RhoB mRNA and protein. Inhibiting hypoxia-activated hypoxia-inducible transcription factor-1α (HIF-1α), c-Jun N-terminal kinase (JNK) or extracellular signal-regulated kinase (ERK) with their specific inhibitors significantly decreased hypoxia-induced RhoB expression, indicating that HIF-1α, JNK and ERK are involved in the up-regulation of RhoB in hypoxia. Furthermore, we found that knockdown of RhoB expression by RhoB siRNA not only significantly reduced hypoxia-enhanced cell migration and cell survival in hypoxia but also increased the sensitivity of cell to paclitaxel (PTX), a chemotherapeutic agent, and reduced Dex-enhanced resistance to PTX-chemotherapy in A549 cells. Taken together, the novel data revealed that hypoxia and Dex increased the expression and activation of RhoB, which is important for hypoxic adaptation and hypoxia-accelerated progression of lung cancer cells. RhoB also enhanced the resistance of cell to PTX-chemotherapy and mediated the pro-survival effect of Dex.<br /> (© 2016 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.)
- Subjects :
- A549 Cells
Animals
Antineoplastic Agents pharmacology
Cell Hypoxia drug effects
Cell Hypoxia genetics
Cell Movement drug effects
Cell Survival drug effects
Dexamethasone pharmacology
Drug Resistance, Neoplasm drug effects
Extracellular Signal-Regulated MAP Kinases metabolism
Hypoxia-Inducible Factor 1, alpha Subunit metabolism
JNK Mitogen-Activated Protein Kinases metabolism
Lung drug effects
Models, Biological
RNA Stability drug effects
RNA, Messenger genetics
RNA, Messenger metabolism
Rats, Sprague-Dawley
p38 Mitogen-Activated Protein Kinases metabolism
rhoB GTP-Binding Protein genetics
Glucocorticoids pharmacology
Lung metabolism
Up-Regulation drug effects
rhoB GTP-Binding Protein metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1582-4934
- Volume :
- 20
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Journal of cellular and molecular medicine
- Publication Type :
- Academic Journal
- Accession number :
- 26915688
- Full Text :
- https://doi.org/10.1111/jcmm.12809