Thornton Tina M, Rincon Mercedes
Department of Medicine/Immunobiology Program, University of Vermont, Burlington, Vermont 05405-0068, USA.
Int J Biol Sci. 2009;5(1):44-51. doi: 10.7150/ijbs.5.44. Epub 2008 Dec 19.
The p38 MAPK kinase pathway is activated in response to a wide range of cellular stress stimuli and cytokines. Our understanding of the important functions of p38 MAPK in the process of differentiation and cell death has grown considerably in the recent years and is now relatively established. Here we discuss the role of p38 MAPK in the mediation of cell cycle checkpoints and cell survival, processes that have received less attention. We describe how p38 MAPK regulates both the G2/M as well as a G1/S cell cycle checkpoint in response to cellular stress such as DNA damage. While p38 MAPK has classically been associated with the induction of apoptosis, we discuss that p38 MAPK can also mediate cell survival in specific situations, such as in response to DNA damage. It is important to recognize these less appreciated functions of p38 MAPK when considering the potential use of pharmacological inhibitors of p38 MAPK in therapeutic treatments for disease.
p38丝裂原活化蛋白激酶(MAPK)信号通路可被多种细胞应激刺激和细胞因子激活。近年来,我们对p38 MAPK在分化和细胞死亡过程中的重要功能的理解有了显著增长,并且现在相对较为明确。在此,我们讨论p38 MAPK在介导细胞周期检查点和细胞存活中的作用,而这些过程此前较少受到关注。我们描述了p38 MAPK如何响应诸如DNA损伤等细胞应激来调节G2/M期以及G1/S期细胞周期检查点。虽然传统上p38 MAPK与细胞凋亡的诱导相关,但我们讨论了p38 MAPK在特定情况下也可介导细胞存活,比如在响应DNA损伤时。在考虑将p38 MAPK的药理学抑制剂用于疾病治疗时,认识到p38 MAPK这些较少被重视的功能非常重要。