Chen Beibei, Hu Huihui, Chen Xiaobing
Department of Medical Oncology, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, Zhengzhou, Henan, China.
Zhengzhou Key Laboratory for Precision Therapy of Gastrointestinal Cancer, Zhengzhou, Henan, China.
Front Genet. 2023 Feb 24;14:1110656. doi: 10.3389/fgene.2023.1110656. eCollection 2023.
Cancerous inhibitor of protein phosphatase 2A (CIP2A), initially reported as a tumor-associated antigen (known as p90), is highly expressed in most solid and hematological tumors. The interaction of CIP2A/p90, protein phosphatase 2A (PP2A), and c-Myc can hinder the function of PP2A toward c-Myc S62 induction, thus stabilizing c-Myc protein, which represents a potential role of CIP2A/p90 in tumorigeneses such as cell proliferation, invasion, and migration, as well as cancer drug resistance. The signaling pathways and regulation networks of CIP2A/p90 are complex and not yet fully understood. Many previous studies have also demonstrated that CIP2A/p90 can be used as a potential therapeutic cancer target. In addition, the autoantibody against CIP2A/p90 in sera may be used as a promising biomarker in the diagnosis of certain types of cancer. In this Review, we focus on recent advances relating to CIP2A/p90 and their implications for future research.
蛋白磷酸酶2A的癌性抑制剂(CIP2A),最初作为一种肿瘤相关抗原(称为p90)被报道,在大多数实体瘤和血液系统肿瘤中高表达。CIP2A/p90、蛋白磷酸酶2A(PP2A)和c-Myc之间的相互作用会阻碍PP2A对c-Myc S62磷酸化的作用,从而使c-Myc蛋白稳定,这表明CIP2A/p90在肿瘤发生过程中具有潜在作用,如细胞增殖、侵袭和迁移,以及癌症耐药性。CIP2A/p90的信号通路和调控网络复杂,尚未完全明确。此前许多研究也表明,CIP2A/p90可用作潜在的癌症治疗靶点。此外,血清中针对CIP2A/p90的自身抗体可能作为某些类型癌症诊断中有前景的生物标志物。在本综述中,我们重点关注CIP2A/p90的最新研究进展及其对未来研究的意义。