State Key Laboratory of Biotherapy, Division of Morbid Genomics, Department of Medical Genetics, West China Hospital, Sichuan University, Chengdu, China.
PLoS One. 2012;7(1):e30999. doi: 10.1371/journal.pone.0030999. Epub 2012 Jan 27.
Piwi proteins have been implicated in germ cell proliferation, differentiation, germline stem cell maintenance and transposon control in germline from Drosophila to mammals. The Piwi-like2 (piwil2) gene is mainly expressed in testis or embryonic cells among normal tissues but widely expressed in tumors. However, it remains to be fully determined through which mechanism piwil2 is involved in tumorigenesis. Here we report that Human piwil2, or Hili represses the tumor suppressor P53 in human cancer cells. Immunoprecipitation analysis shows that Piwil2 can directly associate with Signal Transducer and Activator of Transcription 3 (STAT3) protein via its PAZ domain and form a Piwil2/STAT3/c-Src triple protein-protein complex. Furthermore, STAT3 is phosphorylated by c-Src and translocated to nucleus, then binds to P53 promoter and represses its transcription. The present study demonstrated that Piwil2 plays a role in anti-apoptosis in tumor cells possessing P53 as a positive regulator of STAT3 signaling pathway, providing novel sights into roles of Piwil2 in tumorigenesis.
Piwi 蛋白参与了从果蝇到哺乳动物的生殖细胞增殖、分化、生殖干细胞维持和转座子调控。Piwi 样 2(piwil2)基因在正常组织中的睾丸或胚胎细胞中主要表达,但在肿瘤中广泛表达。然而,piwil2 通过何种机制参与肿瘤发生仍有待充分确定。在这里,我们报告人类 piwil2(Hili)可抑制人癌细胞中的肿瘤抑制因子 P53。免疫沉淀分析表明,Piwil2 通过其 PAZ 结构域与信号转导和转录激活因子 3(STAT3)蛋白直接结合,并形成 Piwil2/STAT3/c-Src 三蛋白-蛋白复合物。此外,STAT3 被 c-Src 磷酸化并转位到细胞核,然后与 P53 启动子结合并抑制其转录。本研究表明,Piwil2 在具有 P53 的肿瘤细胞中发挥抗凋亡作用,作为 STAT3 信号通路的正调控因子,为 Piwil2 在肿瘤发生中的作用提供了新的视角。