Song Fei, Dai Qingqing, Grimm Marc-Oliver, Steinbach Daniel
Department of Urology, Jena University Hospital, 07740 Jena, Germany.
Department of Internal Medicine IV (Gastroenterology, Hepatology, and Infectious Diseases), Jena University Hospital, 07740 Jena, Germany.
Cancers (Basel). 2023 Feb 9;15(4):1115. doi: 10.3390/cancers15041115.
The scaffold protein family of IQ motif-containing GTPase-activating proteins (IQGAP1, 2, and 3) share a high degree of homology and comprise six functional domains. IQGAPs bind and regulate the cytoskeleton, interact with MAP kinases and calmodulin, and have GTPase-related activity, as well as a RasGAP domain. Thus, IQGAPs regulate multiple cellular processes and pathways, affecting cell division, growth, cell-cell interactions, migration, and invasion. In the past decade, significant evidence on the function of IQGAPs in signal transduction during carcinogenesis has emerged. Compared with IQGAP1, IQGAP2 and IQGAP3 were less analyzed. In this review, we summarize the different signaling pathways affected by IQGAP2 and IQGAP3, and the antithetic roles of IQGAP2 and IQGAP3 in different types of cancer. IQGAP2 expression is reduced and plays a tumor suppressor role in most solid cancer types, while IQGAP3 is overexpressed and acts as an oncogene. In lymphoma, for example, IQGAPs have partially opposite functions. There is considerable evidence that IQGAPs regulate a multitude of pathways to modulate cancer processes and chemoresistance, but some questions, such as how they trigger this signaling, through which domains, and why they play opposite roles on the same pathways, are still unanswered.
含IQ模体的GTP酶激活蛋白支架蛋白家族(IQGAP1、2和3)具有高度同源性,由六个功能域组成。IQGAP可结合并调节细胞骨架,与丝裂原活化蛋白激酶(MAP激酶)和钙调蛋白相互作用,具有GTP酶相关活性以及一个RasGAP结构域。因此,IQGAP调节多种细胞过程和信号通路,影响细胞分裂、生长、细胞间相互作用、迁移和侵袭。在过去十年中,出现了大量关于IQGAP在致癌过程中信号转导功能的证据。与IQGAP1相比,对IQGAP2和IQGAP3的分析较少。在本综述中,我们总结了受IQGAP2和IQGAP3影响的不同信号通路,以及IQGAP2和IQGAP3在不同类型癌症中的相反作用。IQGAP2表达降低,在大多数实体癌类型中发挥肿瘤抑制作用,而IQGAP3过表达并充当癌基因。例如,在淋巴瘤中,IQGAP具有部分相反的功能。有大量证据表明,IQGAP调节多种信号通路以调节癌症进程和化疗耐药性,但一些问题,如它们如何触发这种信号传导、通过哪些结构域以及为什么它们在相同信号通路上发挥相反作用,仍然没有答案。