Hlobilková Alice, Knillová Jana, Bártek Jirí, Lukás Jirí, Kolár Zdenek
Institute of Pathology and Laboratory of Molecular Pathology, Faculty of Medicine, Palacký University, Hnevotínská 3, 775 15 Olomouc, Czech Republic.
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2003 Nov;147(1):19-25.
Intracellular levels of phosphorylation are regulated by the coordinated action of protein kinases and phosphatases. Disregulation of this balance can lead to cellular transformation. Here we review knowledge of the mechanisms of one protein phosphatase, the tumour suppressor PTEN/MMAC/TEP 1 apropos its role in tumorigenesis and signal transduction. PTEN plays an important role in the phosphatidyl-inositol-3-kinase (PI3-K) pathway by catalyzing degradation of phosphatidylinositol-(3,4,5)-triphosphate generated by PI3-K. This inhibits downstream targets mainly protein kinase B (PKB/Akt), cell survival and proliferation. PTEN contributes to cell cycle regulation by blockade of cells entering the S phase of the cell cycle, and by upregulation of p27(Kip1) which is recruited into the cyclin E/cdk2 complex. PTEN also modulates cell migration and motility by regulation of the extracellular signal-related kinase - mitogen activated protein kinase (ERK-MAPK) pathway and by dephosphorylation of focal adhesion kinase (FAK). We also emphasize the increasingly important role that PTEN has from an evolutionary point of view. A number of PTEN functions have been elucidated but more information is needed for utilization in clinical application and potential cancer therapy.
细胞内的磷酸化水平由蛋白激酶和磷酸酶的协同作用调节。这种平衡的失调会导致细胞转化。在此,我们综述了一种蛋白磷酸酶——肿瘤抑制因子PTEN/MMAC/TEP 1在肿瘤发生和信号转导中的作用机制的相关知识。PTEN通过催化磷脂酰肌醇-3-激酶(PI3-K)产生的磷脂酰肌醇-(3,4,5)-三磷酸的降解,在磷脂酰肌醇-3-激酶(PI3-K)途径中发挥重要作用。这抑制了下游靶点,主要是蛋白激酶B(PKB/Akt)、细胞存活和增殖。PTEN通过阻止细胞进入细胞周期的S期以及上调被招募到细胞周期蛋白E/细胞周期蛋白依赖性激酶2(cyclin E/cdk2)复合物中的p27(Kip1),促进细胞周期调控。PTEN还通过调节细胞外信号相关激酶-丝裂原活化蛋白激酶(ERK-MAPK)途径以及粘着斑激酶(FAK)的去磷酸化来调节细胞迁移和运动。我们还强调了从进化角度来看PTEN日益重要的作用。虽然已经阐明了PTEN的许多功能,但在临床应用和潜在癌症治疗中的应用还需要更多信息。