c-Src-p38 Mitogen-Activated Protein Kinase Signaling Is Required for Akt Activation in Response to Ionizing Radiation

• Published in: Molecular cancer research 2008-12, Vol.6 (12), p.1872-1880
• Main Authors: Kim, Min-Jung, Byun, Joo-Yun, Yun, Chang-Hwan, Park, In-Chul, Lee, Kee-Ho, Lee, Su-Jae
• Format: Article
• Language: English
• Subjects: c-Src-Rac1-p38 MAPK-mediated Ser473 phosphorylation of Akt; Cell Survival - physiology; Cell Survival - radiation effects; cell survival against radiation; Female; HeLa Cells; Humans; MAP Kinase Signaling System - physiology; MAP Kinase Signaling System - radiation effects; p38 Mitogen-Activated Protein Kinases - metabolism; Phosphorylation - physiology; Phosphorylation - radiation effects; Proto-Oncogene Proteins c-akt - metabolism; Proto-Oncogene Proteins pp60(c-src) - metabolism; rac1 GTP-Binding Protein - metabolism; Radiation, Ionizing; radiation-induced Akt activation; Serine - metabolism; Uterine Cervical Neoplasms - metabolism; Uterine Cervical Neoplasms - pathology; Uterine Cervical Neoplasms - radiotherapy
• ISSN: 1541-7786; 1557-3125
• DOI: 10.1158/1541-7786.MCR-08-0084

The Akt and mitogen-activated protein kinase (MAPK) pathways have been implicated in tumor cell survival and contribute to radiation resistance. However, the molecular basis for link between MAPK and Akt in cell survival response to radiation is unclear. Here, we show that c-Src-Rac1-p38 MAPK pathway signals Akt activation and cell survival in response to radiation. Ionizing radiation triggered Thr 308 and Ser 473 phosphorylation of Akt. Exposure of cells to radiation also induced p38 MAPK and c-Jun NH 2 -terminal kinase activations. Inhibition of c-Jun NH 2 -terminal kinase suppressed radiation-induced cell death, whereas inhibition of p38 MAPK effectively increased sensitivity to radiation. Interestingly, inhibition of p38 MAPK completely attenuated radiation-induced Ser 473 phosphorylation of Akt but did not affect Thr 308 phosphorylation. Conversely, overexpression of p38 MAPK enhanced Ser 473 phosphorylation of Akt in response to radiation. In addition, inhibition of p38 MAPK failed to alter phosphoinositide 3-kinase and phosphoinositide-dependent protein kinase activities. Ectopic expression of RacN17, dominant-negative form of Rac1, inhibited p38 MAPK activation and Ser 473 phosphorylation of Akt. Following exposure to radiation, c-Src was selectively activated among Src family tyrosine kinases. Inhibition of c-Src attenuated Rac1 and p38 MAPK activations and Ser 473 phosphorylation of Akt. Our results support the notion that the c-Src-Rac1-p38 MAPK pathway is required for activation of Akt in response to radiation and plays a cytoprotective role against radiation in human cancer cells. (Mol Cancer Res 2008;6(12):1872–80)