Department of Oncology, Shanghai Tongren Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
J Cell Physiol. 2024 Nov;239(11):e31413. doi: 10.1002/jcp.31413. Epub 2024 Aug 16.
The protein phosphatase 2A (PP2A), a serine/threonine phosphatase, is recognized as a tumor suppressor involved in diverse cellular processes and essential for maintaining cell viability in vivo. However, endogenous inhibitors of PP2A such as cancerous inhibitor of PP2A (CIP2A) and endogenous nuclear protein inhibitor 2 of PP2A (SET) counteract the anticancer function of PP2A, promoting tumorigenesis, development, and drug resistance in tumors. Surprisingly though, contrary to conventional understanding, inhibition of the tumor suppressor gene PP2A with exogenous small molecule compounds can enhance the efficacy of cancer treatment and achieve superior tumor inhibition. Moreover, exogenous PP2A inhibitors resensitize cancers to treatment and provide novel therapeutic strategies for drug-resistant tumors, which warrant further investigation.
蛋白磷酸酶 2A(PP2A)是一种丝氨酸/苏氨酸磷酸酶,被认为是一种肿瘤抑制因子,参与多种细胞过程,对于维持体内细胞活力至关重要。然而,PP2A 的内源性抑制剂,如癌性 PP2A 抑制剂(CIP2A)和内源性核蛋白 PP2A 抑制剂 2(SET),会抵消 PP2A 的抗癌功能,促进肿瘤的发生、发展和耐药性。但令人惊讶的是,与传统观点相反,用外源性小分子化合物抑制肿瘤抑制基因 PP2A 可以增强癌症治疗的效果,实现更优的肿瘤抑制。此外,外源性 PP2A 抑制剂可以使癌症对治疗重新敏感,并为耐药性肿瘤提供新的治疗策略,值得进一步研究。