Kostenko Sergiy, Dumitriu Gianina, Moens Ugo
Department of Medical Biology, Faculty of Health Sciences, University of Tromsø, Tromsø, NO-9037, Norway.
J Mol Signal. 2012 Jul 16;7(1):9. doi: 10.1186/1750-2187-7-9.
Perturbed action of signal transduction pathways, including the mitogen-activated protein (MAP) kinase pathways, is one of the hallmarks of many cancers. While the implication of the typical MAP kinase pathways ERK1/2-MEK1/2, p38MAPK and JNK is well established, recent findings illustrate that the atypical MAP kinase ERK3/4-MK5 may also be involved in tumorigenic processes. Remarkably, the ERK3/4-MK5 pathway seems to possess anti-oncogenic as well as pro-oncogenic properties in cell culture and aninal models. This review summarizes the mutations in the genes encoding ERK3, ERK4 and MK5 that have been detected in different cancers, reports aberrant expression levels of these proteins in human tumours, and discusses the mechanisms by which this pathway can induce senescence, stimulate angiogenesis and invasiveness.
信号转导通路的紊乱,包括丝裂原活化蛋白(MAP)激酶通路,是许多癌症的标志之一。虽然典型的MAP激酶通路ERK1/2-MEK1/2、p38MAPK和JNK的作用已得到充分证实,但最近的研究结果表明,非典型MAP激酶ERK3/4-MK5也可能参与肿瘤发生过程。值得注意的是,在细胞培养和动物模型中,ERK3/4-MK5通路似乎具有抗癌和促癌特性。本综述总结了在不同癌症中检测到的编码ERK3、ERK4和MK5的基因突变,报道了这些蛋白在人类肿瘤中的异常表达水平,并讨论了该通路诱导衰老、刺激血管生成和侵袭的机制。