He Shengnan, Liu Feng, Xie Zhenhua, Zu Xuyu, Xu Wei, Jiang Yuyang
The Key Laboratory of Chemical Biology, Guangdong Province, Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055, Guangdong, China; E-Mail:
Int J Mol Sci. 2010 Aug 27;11(9):3309-051. doi: 10.3390/ijms11093039.
P-glycoprotein (Pgp), encoded by the multidrug resistance 1 (MDR1) gene, is an efflux transporter and plays an important role in pharmacokinetics. In this study, we demonstrated that the pokemon promoter activity, the pokemon mRNA and protein expression can be significantly inhibited by Pgp. Chromatin immunoprecipitation assay showed that Pgp can bind the pokemon prompter to repress pokemon transcription activity. Furthermore, Pgp regulated pokemon transcription activity through expression of p53 as seen by use of p53 siRNA transfected MCF-7 cells or p53 mutated MDA-MB-231 cells. Moreover, p53 was detected to bind with Pgp in vivo using immunoprecipitation assay. Taken together, we conclude that Pgp can regulate the expression of pokemon through the presence of p53, suggesting that Pgp is a potent regulator and may offer an effective novel target for cancer therapy.
由多药耐药基因1(MDR1)编码的P-糖蛋白(Pgp)是一种外排转运蛋白,在药代动力学中起重要作用。在本研究中,我们证明Pgp可显著抑制口袋妖怪启动子活性、口袋妖怪mRNA和蛋白表达。染色质免疫沉淀分析表明,Pgp可与口袋妖怪启动子结合以抑制口袋妖怪转录活性。此外,如通过使用转染p53小干扰RNA的MCF-7细胞或p53突变的MDA-MB-231细胞所见,Pgp通过p53的表达调节口袋妖怪转录活性。而且,使用免疫沉淀分析在体内检测到p53与Pgp结合。综上所述,我们得出结论,Pgp可通过p53的存在调节口袋妖怪的表达,提示Pgp是一种有效的调节因子,可能为癌症治疗提供一个有效的新靶点。 (注:原文中“pokemon”可能有误,推测是“p53”,这里按照原文翻译)