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丝氨酸/苏氨酸蛋白磷酸酶2A在癌症中的作用。

Role of serine/threonine protein phosphatase 2A in cancer.

作者信息

Schönthal A H

机构信息

Department of Molecular Microbiology and Immunology, Keck School of Medicine, University of Southern California, 2011 Zonal Avenue, HMR-405, Los Angeles, CA 90033, USA.

出版信息

Cancer Lett. 2001 Sep 10;170(1):1-13. doi: 10.1016/s0304-3835(01)00561-4.

Abstract

The serine/threonine protein phosphatase 2A (PP2A) appears to be critically involved in cellular growth control and potentially in the development of cancer. A few studies indicated that this enzyme might actually exert tumor suppressive function. However, other findings demonstrated the requirement for PP2A in cell growth and survival, which is not a characteristic of a typical tumor suppressor. This apparent discrepancy might be due to the fact that PP2A is a multitask enzyme system, rather than a single enzyme. Its individual subunits are encoded by a heterogeneous group of genes which give rise to a multitude of different PP2A holoenzyme complexes. Thus, the puzzling observation that PP2A exerts inhibitory, as well as stimulatory, effects on cell growth could be due to the activity of different PP2A complexes with distinct subcellular location and divers substrate specificity. At the same time, this abundance of PP2A components provides a large target for mutations that might derail proper enzyme function and could contribute to the process of tumorigenesis. So far, however, it has not been unequivocally established whether such mutations, examples of which have indeed been found in human cancer cells, result in the activation of an oncogenic function or rather in the inactivation of the presumed tumor suppressive role of PP2A. Therefore, the general opinion of PP2A as being a tumor suppressor needs to be viewed with caution.

摘要

丝氨酸/苏氨酸蛋白磷酸酶2A(PP2A)似乎在细胞生长控制中起关键作用,并可能与癌症的发生发展有关。一些研究表明,这种酶实际上可能发挥肿瘤抑制功能。然而,其他研究结果显示PP2A在细胞生长和存活中是必需的,而这并非典型肿瘤抑制因子的特征。这种明显的差异可能是由于PP2A是一个多任务酶系统,而非单一的酶。其各个亚基由一组异质基因编码,这些基因产生大量不同的PP2A全酶复合物。因此,PP2A对细胞生长既发挥抑制作用又发挥刺激作用这一令人困惑的观察结果,可能是由于具有不同亚细胞定位和多样底物特异性的不同PP2A复合物的活性所致。与此同时,PP2A成分的丰富性为可能破坏酶正常功能并可能促进肿瘤发生过程的突变提供了大量靶点。然而,到目前为止,尚未明确确定在人类癌细胞中确实发现的此类突变是导致致癌功能的激活,还是导致PP2A假定的肿瘤抑制作用失活。因此,对于PP2A作为肿瘤抑制因子的普遍观点需要谨慎看待。

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