PP2A 抑制的矛盾作用及其治疗增敏的潜力。

IF 4.5 2区 生物学 Q2 CELL BIOLOGY Journal of Cellular Physiology Pub Date : 2024-08-16 DOI:10.1002/jcp.31413
Yue Jiang, Ying Yuan, Guanglei Qiao, Zhoufeng Deng, Zimei Liu, Yan Zhang, Liping Yu, Hongjian Lin, Lijun Ma, Jianjun Zhang
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引用次数: 0

摘要

蛋白磷酸酶 2A(PP2A)是一种丝氨酸/苏氨酸磷酸酶,是公认的肿瘤抑制因子,参与多种细胞过程,对维持体内细胞活力至关重要。然而,PP2A 的内源性抑制剂,如 PP2A 的癌症抑制剂(CIP2A)和 PP2A 的内源性核蛋白抑制剂 2(SET),会抵消 PP2A 的抗癌功能,促进肿瘤的发生、发展和耐药性。但令人惊奇的是,与传统认识相反,用外源性小分子化合物抑制肿瘤抑制基因 PP2A 可以提高癌症治疗的疗效,实现卓越的肿瘤抑制效果。此外,外源性 PP2A 抑制剂可使癌症对治疗重新敏感,为耐药性肿瘤提供了新的治疗策略,值得进一步研究。
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Paradoxical action of PP2A inhibition and its potential for therapeutic sensitization

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.

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来源期刊
CiteScore
14.70
自引率
0.00%
发文量
256
审稿时长
1 months
期刊介绍: The Journal of Cellular Physiology publishes reports of high biological significance in areas of eukaryotic cell biology and physiology, focusing on those articles that adopt a molecular mechanistic approach to investigate cell structure and function. There is appreciation for the application of cellular, biochemical, molecular and in vivo genetic approaches, as well as the power of genomics, proteomics, bioinformatics and systems biology. In particular, the Journal encourages submission of high-interest papers investigating the genetic and epigenetic regulation of proliferation and phenotype as well as cell fate and lineage commitment by growth factors, cytokines and their cognate receptors and signal transduction pathways that influence the expression, integration and activities of these physiological mediators. Similarly, the Journal encourages submission of manuscripts exploring the regulation of growth and differentiation by cell adhesion molecules in addition to the interplay between these processes and those induced by growth factors and cytokines. Studies on the genes and processes that regulate cell cycle progression and phase transition in eukaryotic cells, and the mechanisms that determine whether cells enter quiescence, proliferate or undergo apoptosis are also welcomed. Submission of papers that address contributions of the extracellular matrix to cellular phenotypes and physiological control as well as regulatory mechanisms governing fertilization, embryogenesis, gametogenesis, cell fate, lineage commitment, differentiation, development and dynamic parameters of cell motility are encouraged. Finally, the investigation of stem cells and changes that differentiate cancer cells from normal cells including studies on the properties and functions of oncogenes and tumor suppressor genes will remain as one of the major interests of the Journal.
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