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P38 and JNK MAPK pathways control the balance of apoptosis and autophagy in response to chemotherapeutic agents

机译:P38和JNK MAPK通路控制对化疗药物的凋亡和自噬的平衡

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摘要

The Mitogen Activated Protein Kinase (MAPK) signaling plays a critical role in the outcome and the sensitivity to anticancer therapies. Activated MAPK can transmit extracellular signals to regulate cell growth, proliferation, differentiation, migration, apoptosis and so on. Apoptosis as well as macroautophagy (hereafter referred to as autophagy) can be induced by extracellular stimuli such the treatment of chemotherapeutic agents, resulting in different cell response to these drugs. However, the molecular mechanisms mediating these two cellular processes remain largely unknown. Recently, several studies provide new insights into p38 and JNK MAPK pathways function in the control of the balance of autophagy and apoptosis in response to genotoxic stress. Our increased understanding of the role of p38 and JNK MAPK pathways in regulating the balance of autophagy and apoptosis will hopefully provide prospective strategies for cancer therapy.
机译:丝裂原活化蛋白激酶(MAPK)信号在结局和对抗癌疗法的敏感性中起关键作用。活化的MAPK可以传递细胞外信号来调节细胞的生长,增殖,分化,迁移,凋亡等。细胞凋亡以及宏自噬(以下称为自噬)可以通过细胞外刺激来诱导,例如化学治疗剂的处理,导致对这些药物的不同细胞应答。然而,介导这两个细胞过程的分子机制仍然是未知的。最近,一些研究提供了对p38和JNK MAPK通路在控制遗传毒性应激反应中自噬和凋亡平衡中的功能的新见解。我们对p38和JNK MAPK途径在调节自噬和细胞凋亡平衡中作用的深入了解有望为癌症治疗提供前瞻性策略。

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