Cao JingPing, Zhu Shu, Zhou Wei, Li Jie, Liu Chang, Xuan HanQing, Yan Jie, Zheng Lin, Zhou LiXin, Yu JianXiu, Chen GuoQiang, Huang YiRan, Yu Zhuo, Feng LiXin
Institute of Health Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences & Shanghai Jiao Tong University School of Medicine, Shanghai, China ; Laboratory for Germ Cell Research, Institute of Medical Sciences, Shanghai Jiao Tong University School of Medicine (SJTU-SM), Shanghai, China ; Department of Pathophysiology, Key Laboratory of Cell Differentiation and Apoptosis of Chinese Ministry of Education, SJTU-SM, Shanghai, China.
PLoS One. 2013 Dec 10;8(12):e77922. doi: 10.1371/journal.pone.0077922. eCollection 2013.
Promyelocytic leukemia zinc finger (PLZF) protein expression is closely related to the progression of human cancers, including prostate cancer (PCa). However, the according context of a signaling pathway for PLZF to suppress prostate tumorigenesis remains greatly unknown. Here we report that PLZF is a downstream mediator of the PTEN signaling pathway in PCa. We found that PLZF expression is closely correlated with PTEN expression in a cohort of prostate cancer specimens. Interestingly, both PTEN rescue and phosphoinositide 3-kinase (PI3K) inhibitor LY294002 treatment increase the PLZF expression in prostate cancer cell lines. Further, luciferase reporter assay and chromatin immunoprecipitation assay demonstrate that FOXO3a, a transcriptional factor phosphorylated by PI3K/AKT, could directly bind to the promoter of PLZF gene. These results indicate that PTEN regulates PLZF expression by AKT/FOXO3a. Moreover, our animal experiments also demonstrate that PLZF is capable of inhibiting prostate tumorigenesis in vivo. Taken together, our study defines a PTEN/PLZF pathway and would shed new lights for developing therapeutic strategy of prostate cancer.
早幼粒细胞白血病锌指蛋白(PLZF)的表达与包括前列腺癌(PCa)在内的人类癌症进展密切相关。然而,PLZF抑制前列腺肿瘤发生的信号通路相关背景仍知之甚少。在此,我们报告PLZF是前列腺癌中PTEN信号通路的下游介质。我们发现,在一组前列腺癌标本中,PLZF表达与PTEN表达密切相关。有趣的是,PTEN挽救和磷酸肌醇3激酶(PI3K)抑制剂LY294002处理均能增加前列腺癌细胞系中PLZF的表达。此外,荧光素酶报告基因检测和染色质免疫沉淀检测表明,被PI3K/AKT磷酸化的转录因子FOXO3a可直接结合到PLZF基因的启动子上。这些结果表明,PTEN通过AKT/FOXO3a调节PLZF表达。此外,我们的动物实验还表明,PLZF在体内能够抑制前列腺肿瘤发生。综上所述,我们的研究确定了一条PTEN/PLZF通路,并将为前列腺癌治疗策略的开发提供新的思路。