García-Flores Natalia, Jiménez-Suárez Jaime, Garnés-García Cristina, Fernández-Aroca Diego M, Sabater Sebastia, Andrés Ignacio, Fernández-Aramburo Antonio, Ruiz-Hidalgo María José, Belandia Borja, Sanchez-Prieto Ricardo, Cimas Francisco J
Laboratorio 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.
Servicio de Oncología Radioterápica, Complejo Hospitalario Universitario de Albacete, 02006 Albacete, Spain.
Cancers (Basel). 2023 Jan 30;15(3):861. doi: 10.3390/cancers15030861.
Over the last 30 years, the study of the cellular response to ionizing radiation (IR) has increased exponentially. Among the various signaling pathways affected by IR, p38 MAPK has been shown to be activated both in vitro and in vivo, with involvement in key processes triggered by IR-mediated genotoxic insult, such as the cell cycle, apoptosis or senescence. However, we do not yet have a definitive clue about the role of p38 MAPK in terms of radioresistance/sensitivity and its potential use to improve current radiotherapy. In this review, we summarize the current knowledge on this family of MAPKs in response to IR as well as in different aspects related to radiotherapy, such as their role in the control of REDOX, fibrosis, and in the radiosensitizing effect of several compounds.
在过去30年中,对细胞对电离辐射(IR)反应的研究呈指数级增长。在受IR影响的各种信号通路中,p38丝裂原活化蛋白激酶(p38 MAPK)已被证明在体外和体内均被激活,并参与由IR介导的遗传毒性损伤引发的关键过程,如细胞周期、细胞凋亡或衰老。然而,就抗辐射性/敏感性而言,我们尚未明确p38 MAPK的作用及其在改善当前放射治疗方面的潜在用途。在本综述中,我们总结了关于这一MAPK家族对IR反应的当前知识,以及与放射治疗相关的不同方面,如它们在氧化还原控制、纤维化以及几种化合物的放射增敏作用中的作用。