Low Heng Boon, Zhang Yongliang
Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, Singapore.; Immunology Programme, The Life Science Institute, National University of Singapore, Singapore 117597, Singapore.
Immune Netw. 2016 Apr;16(2):85-98. doi: 10.4110/in.2016.16.2.85. Epub 2016 Apr 28.
The mitogen-activated protein kinases (MAPKs) are key regulators of cell growth and survival in physiological and pathological processes. Aberrant MAPK signaling plays a critical role in the development and progression of human cancer, as well as in determining responses to cancer treatment. The MAPK phosphatases (MKPs), also known as dual-specificity phosphatases (DUSPs), are a family of proteins that function as major negative regulators of MAPK activities in mammalian cells. Studies using mice deficient in specific MKPs including MKP1/DUSP1, PAC-1/DUSP2, MKP2/DUSP4, MKP5/DUSP10 and MKP7/DUSP16 demonstrated that these molecules are important not only for both innate and adaptive immune responses, but also for metabolic homeostasis. In addition, the consequences of the gain or loss of function of the MKPs in normal and malignant tissues have highlighted the importance of these phosphatases in the pathogenesis of cancers. The involvement of the MKPs in resistance to cancer therapy has also gained prominence, making the MKPs a potential target for anti-cancer therapy. This review will summarize the current knowledge of the MKPs in cancer development, progression and treatment outcomes.
丝裂原活化蛋白激酶(MAPKs)是生理和病理过程中细胞生长与存活的关键调节因子。异常的MAPK信号传导在人类癌症的发生和发展以及决定癌症治疗反应中起着关键作用。MAPK磷酸酶(MKPs),也称为双特异性磷酸酶(DUSPs),是一类蛋白质,在哺乳动物细胞中作为MAPK活性的主要负调节因子发挥作用。使用缺乏特定MKPs(包括MKP1/DUSP1、PAC-1/DUSP2、MKP2/DUSP4、MKP5/DUSP10和MKP7/DUSP16)的小鼠进行的研究表明,这些分子不仅对先天性和适应性免疫反应很重要,而且对代谢稳态也很重要。此外,MKPs在正常和恶性组织中功能获得或丧失的后果凸显了这些磷酸酶在癌症发病机制中的重要性。MKPs参与癌症治疗耐药性也日益突出,使MKPs成为抗癌治疗的潜在靶点。本综述将总结目前关于MKPs在癌症发生、发展和治疗结果方面的知识。