Guerrero David, Guarch Rosa, Ojer Amaya, Casas Juan Manuel, Ropero Santiago, Mancha Ana, Pesce Carlo, Lloveras Belen, Garcia-Bragado Federico, Puras Ana
Biomedical Research Center, Navarra Health Service, Pamplona, Navarra, Spain.
BJU Int. 2008 Sep;102(6):747-55. doi: 10.1111/j.1464-410X.2008.07603.x. Epub 2008 Mar 10.
To evaluate the presence of human papillomavirus (HPV) infection, the methylation status in the promoter region of thrombospondin-1 (TSP-1), RAS association domain family 1A (RASSF1-A) and p16 genes, and the expression of TSP-1, CD31, p16 and p53 proteins in patients diagnosed with penile cancer, and the possible associations between these variables and clinical and pathological features.
HPV types, gene promoter hypermethylation and protein expression were analysed by reverse line blot, methylation-specific polymerase chain reaction, and immunohistochemistry, respectively, in 24 penile squamous cell carcinomas.
HPV infection was detected in 11 of 24 cases (46%), and TSP-1, RASSF1-A and p16 genes were hypermethylated in 46%, 42% and 38% of the tumours, respectively. TSP-1 hypermethylation was associated with unfavourable histological grade (grade 3; P = 0.033), vascular invasion (P = 0.023), weak expression of TSP-1 protein (P = 0.041), and shorter overall survival (P = 0.04). TSP-1 expression was not associated with microvessel density. However, RASSF1-A hypermethylation was more frequent in T1 tumours (P = 0.01), and p16 hypermethylation was not associated with any of the tested variables except for absence of p16 expression (P = 0.022).
In summary, the epigenetic inactivation of TSP-1 and RASSF1-A genes is associated with pathological variables and seems to be of prognostic significance in penile cancer.
评估阴茎癌患者中人类乳头瘤病毒(HPV)感染情况、血小板反应蛋白-1(TSP-1)、RAS 关联结构域家族 1A(RASSF1-A)和 p16 基因启动子区域的甲基化状态,以及 TSP-1、CD31、p16 和 p53 蛋白的表达情况,并分析这些变量与临床和病理特征之间的可能关联。
分别采用反向线印迹法、甲基化特异性聚合酶链反应和免疫组织化学方法,对 24 例阴茎鳞状细胞癌患者的 HPV 类型、基因启动子高甲基化和蛋白表达进行分析。
24 例患者中有 11 例(46%)检测到 HPV 感染,46%、42%和 38%的肿瘤中 TSP-1、RASSF1-A 和 p16 基因发生高甲基化。TSP-1 高甲基化与不良组织学分级(3 级;P = 0.033)、血管侵犯(P = 0.023)、TSP-1 蛋白弱表达(P = 0.041)及总生存期较短(P = 0.04)相关。TSP-1 表达与微血管密度无关。然而,RASSF1-A 高甲基化在 T1 肿瘤中更常见(P = 0.01),p16 高甲基化除与 p16 表达缺失相关外(P = 0.022),与其他任何检测变量均无关联。
总之,TSP-1 和 RASSF1-A 基因的表观遗传失活与病理变量相关,似乎对阴茎癌具有预后意义。