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Published on: April 5, 2024
P38 MAPK and Radiotherapy: Foes or Friends?
Natalia García-Flores1, Jaime Jiménez-Suárez1, Cristina Garnés-García1
1Laboratorio de Oncología Molecular, Unidad de Medicina Molecular, Centro Regional de Investigaciones Biomédicas, Unidad Asociada de Biomedicina UCLM, Unidad Asociada al CSIC, Universidad de Castilla-La Mancha, 02008 Albacete, Spain.
The p38 MAPK pathway is activated by ionizing radiation (IR) and influences cell cycle, apoptosis, and senescence. Its precise role in radioresistance and potential for improving radiotherapy remain unclear.
Area of Science:
- Cellular Biology
- Radiation Oncology
- Molecular Signaling
Background:
- Cellular response to ionizing radiation (IR) is crucial in radiotherapy.
- The p38 MAPK pathway is activated by IR and affects key cellular processes.
- The exact role of p38 MAPK in radioresistance and radiotherapy improvement is not fully understood.
Purpose of the Study:
- To review the current knowledge on p38 MAPK signaling in response to IR.
- To explore the involvement of p38 MAPK in radiotherapy-related aspects.
- To assess the potential of p38 MAPK as a target for improving radiotherapy.
Main Methods:
- Literature review of studies on p38 MAPK and ionizing radiation.
- Analysis of p38 MAPK's role in cell cycle, apoptosis, and senescence post-IR.
- Examination of p38 MAPK's involvement in REDOX control, fibrosis, and radiosensitization.
Main Results:
- p38 MAPK activation by IR is consistently observed in vitro and in vivo.
- p38 MAPK influences critical cellular responses to genotoxic stress.
- Its precise contribution to radioresistance/sensitivity requires further elucidation.
Conclusions:
- p38 MAPK is a significant player in the cellular response to IR.
- Understanding p38 MAPK's function is vital for optimizing radiotherapy strategies.
- Targeting p38 MAPK may offer novel approaches to enhance radiosensitization.
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