Wang Kun, Liu Tiantian, Ge Nan, Liu Li, Yuan Xiaotian, Liu Jikai, Kong Feng, Wang Chang, Ren Hongbo, Yan Keqiang, Hu Sanyuan, Xu Zhonghua, Björkholm Magnus, Fan Yidong, Zhao Shengtian, Liu Cheng, Xu Dawei
Department of Urology, Shandong University Qilu Hospital, Jinan, China. Department of Medicine, Division of Hematology and Centre for Molecular Medicine, Karolinska University Hospital Solna and Karolinska Institutet, Stockholm, Sweden.
Department of Pathology, Shandong University School of Medicine, Jinan, China.
Oncotarget. 2014 Dec 15;5(23):12428-39. doi: 10.18632/oncotarget.2660.
TERT promoter C228T and C250T mutations occur in various malignancies including bladder cancer (BC) and may serve as urinary tumor markers. However, the mutation association with clinical variables in upper tract urothelial carcinomas (UTUCs) is unclear. There is also a lack of sensitive tools to detect the minor mutant TERT promoter in bulk urinary DNA. Here we analyzed 220 UTUC patients [98 with renal pelvic carcinoma (RPC) and 122 with ureter carcinoma (UC)] and developed a Competitive Allele-Specific TaqMan PCR (castPCR) for urinary assay. We identified C228T or C250T mutations in 42 of 98 (43%) RPC and 23 of 122 (19%) UC tumors. Distant metastases were significantly correlated with UTUC patients harboring TERT promoter mutations (P = 0.001). C228T were detected in 6/10 and 9/10 of urine samples from patients with mutation-carrying tumors using Sanger sequencing and castPCR, respectively. When urine samples from 70 BC patients were analyzed together, the sensitivity of urinary C228T assay was 89% and 50% for castPCR and Sanger sequencing, respectively (P < 0.001). Collectively, TERT promoter mutations occur in UTUCs with a high frequency in RPCs and predict distant metastasis. castPCR assays of the mutation are a useful tool for urine-based diagnostics of urological malignancies.
端粒酶逆转录酶(TERT)启动子C228T和C250T突变存在于包括膀胱癌(BC)在内的多种恶性肿瘤中,可能作为尿肿瘤标志物。然而,在上尿路尿路上皮癌(UTUCs)中,这些突变与临床变量的关联尚不清楚。此外,还缺乏灵敏的工具来检测大量尿DNA中的少量突变TERT启动子。在此,我们分析了220例UTUC患者[98例肾盂癌(RPC)和122例输尿管癌(UC)],并开发了一种用于尿液检测的竞争性等位基因特异性TaqMan PCR(castPCR)。我们在98例RPC肿瘤中的42例(43%)和122例UC肿瘤中的23例(19%)中检测到C228T或C250T突变。远处转移与携带TERT启动子突变的UTUC患者显著相关(P = 0.001)。分别使用Sanger测序和castPCR在携带突变肿瘤患者的6/10和9/10的尿液样本中检测到C228T。当一起分析70例BC患者的尿液样本时,castPCR和Sanger测序检测尿C228T的灵敏度分别为89%和50%(P < 0.001)。总体而言,TERT启动子突变在UTUCs中以较高频率出现在RPCs中,并可预测远处转移。castPCR检测该突变是基于尿液诊断泌尿系统恶性肿瘤的有用工具。