Navarro Alfons, Tejero Rut, Viñolas Nuria, Cordeiro Anna, Marrades Ramon M, Fuster Dolors, Caritg Oriol, Moises Jorge, Muñoz Carmen, Molins Laureano, Ramirez Josep, Monzo Mariano
Molecular Oncology and Embryology Laboratory, Human Anatomy Unit, School of Medicine, University of Barcelona, IDIBAPS, Barcelona, Spain.
Department of Medical Oncology, Institut Clinic Malalties Hemato-Oncològiques (ICMHO), Hospital Clinic de Barcelona, University of Barcelona, IDIBAPS, Barcelona, Spain.
Oncotarget. 2015 Oct 13;6(31):31544-56. doi: 10.18632/oncotarget.3003.
The expression of Piwi-interacting RNAs, small RNAs that bind to PIWI proteins, was until recently believed to be limited to germinal stem cells. We have studied the expression of PIWI genes during human lung embryogenesis and in paired tumor and normal tissue prospectively collected from 71 resected non-small-cell lung cancer patients. The mRNA expression analysis showed that PIWIL1 was highly expressed in 7-week embryos and downregulated during the subsequent weeks of development. PIWIL1 was expressed in 11 of the tumor samples but in none of the normal tissue samples. These results were validated by immunohistochemistry, showing faint cytoplasmic reactivity in the PIWIL1-positive samples. Interestingly, the patients expressing PIWIL1 had a shorter time to relapse (TTR) (p = 0.006) and overall survival (OS) (p = 0.0076) than those without PIWIL1 expression. PIWIL2 and 4 were downregulated in tumor tissue in comparison to the normal tissue (p < 0.001) and the patients with lower levels of PIWIL4 had shorter TTR (p = 0.048) and OS (p = 0.033). In the multivariate analysis, PIWIL1 expression emerged as an independent prognostic marker. Using 5-Aza-dC treatment and bisulfite sequencing, we observed that PIWIL1 expression could be regulated in part by methylation. Finally, an in silico study identified a stem-cell expression signature associated with PIWIL1 expression.
与PIWI蛋白结合的小分子RNA——Piwi相互作用RNA(Piwi-interacting RNAs)的表达,直到最近还被认为仅限于生殖干细胞。我们研究了人肺胚胎发生过程中以及从71例接受手术切除的非小细胞肺癌患者前瞻性收集的配对肿瘤组织和正常组织中PIWI基因的表达。mRNA表达分析表明,PIWIL1在7周龄胚胎中高表达,并在随后的发育周数中下调。PIWIL1在11个肿瘤样本中表达,但在正常组织样本中均未表达。这些结果通过免疫组织化学得到验证,显示PIWIL1阳性样本中有微弱的细胞质反应。有趣的是,与未表达PIWIL1的患者相比,表达PIWIL1的患者复发时间(TTR)更短(p = 0.006),总生存期(OS)更短(p = 0.0076)。与正常组织相比,PIWIL2和PIWIL4在肿瘤组织中下调(p < 0.001),PIWIL4水平较低的患者TTR更短(p = 0.048),OS更短(p = 0.033)。在多变量分析中,PIWIL1表达成为一个独立的预后标志物。通过5-氮杂-2'-脱氧胞苷(5-Aza-dC)处理和亚硫酸氢盐测序,我们观察到PIWIL1表达部分受甲基化调控。最后,一项计算机模拟研究确定了与PIWIL1表达相关的干细胞表达特征。