Wang Kun, Liu Tiantian, Liu Cheng, Meng Yan, Yuan Xiaotian, Liu Li, Ge Nan, Liu Jikai, Wang Chang, Ren Hongbo, Yan Keqiang, Hu Sanyuan, Xu Zhonghua, Fan Yidong, Xu Dawei
Departments of Urology and General Surgery, Qilu Hospital, Department of Pathology, School of Medicine, and Department of Urology, Second Hospital, Shandong University, Jinan, People's Republic of China; Department of Medicine, Division of Hematology and Center for Molecular Medicine, Karolinska University Hospital Solna and Karolinska Institutet, Stockholm, Sweden.
Departments of Urology and General Surgery, Qilu Hospital, Department of Pathology, School of Medicine, and Department of Urology, Second Hospital, Shandong University, Jinan, People's Republic of China; Department of Medicine, Division of Hematology and Center for Molecular Medicine, Karolinska University Hospital Solna and Karolinska Institutet, Stockholm, Sweden
Oncologist. 2015 Mar;20(3):263-9. doi: 10.1634/theoncologist.2014-0391. Epub 2015 Feb 5.
The TERT promoter and FGFR3 gene mutations are two of the most common genetic events in urothelial bladder cancer (UBC), and these mutation assays in patient urine have been shown to be promising biomarkers for UBC diagnosis and surveillance. These results were obtained mainly from studies of patients with UBC in Western countries, and little is known about such information in Han Chinese patients with UBC. In the present study, we addressed this issue by analyzing tumors from 182 Han Chinese patients with UBC and urine samples from 102 patients for mutations in the TERT promoter and FGFR3 and TERT mRNA expression in tumors and/or urine. TERT promoter and FGFR3 mutations were identified in 87 of 182 (47.8%) and 7 of 102 (6.7%) UBC cases, respectively. In 46 urine samples from patients with TERT promoter mutation-carrying tumors, the mutant promoter was detected in 24 (52%) prior to operation and disappeared in most examined urine samples (80%) taken 1 week after operation. TERT mRNA was detected in urine derived from 46 of 49 patients (94%) that was analyzed before operation independently of the presence of TERT promoter mutations. Collectively, FGFR3 mutations occur at a very low rate in Han Chinese UBC and cannot serve as diagnostic markers for Chinese patients. Han Chinese patients with UBC have relatively low TERT promoter mutation frequency compared with patients in Western countries, and simultaneous detection of both mutant TERT promoter and TERT mRNA improves sensitivity and specificity of urine-based diagnosis.
端粒酶逆转录酶(TERT)启动子和成纤维细胞生长因子受体3(FGFR3)基因突变是尿路上皮膀胱癌(UBC)中最常见的两种基因事件,并且已证明患者尿液中的这些突变检测是UBC诊断和监测的有前景的生物标志物。这些结果主要来自西方国家UBC患者的研究,而对于中国汉族UBC患者的此类信息知之甚少。在本研究中,我们通过分析182例中国汉族UBC患者的肿瘤以及102例患者的尿液样本中TERT启动子和FGFR3的突变情况以及肿瘤和/或尿液中TERT mRNA的表达来解决这个问题。在182例UBC病例中的87例(47.8%)和102例中的7例(6.7%)分别检测到TERT启动子和FGFR3突变。在46例携带TERT启动子突变肿瘤患者的尿液样本中,术前在24例(52%)中检测到突变启动子,而在术后1周采集的大多数检测尿液样本(80%)中突变启动子消失。在术前分析的49例患者中的46例(94%)尿液中检测到TERT mRNA,与TERT启动子突变的存在无关。总体而言,FGFR3突变在中国汉族UBC中的发生率非常低,不能作为中国患者的诊断标志物。与西方国家患者相比,中国汉族UBC患者的TERT启动子突变频率相对较低,同时检测突变的TERT启动子和TERT mRNA可提高基于尿液诊断的敏感性和特异性。