Human Oncology & Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Department of Urology, Ludwig-Maximilians University, Munich, Germany.
Urology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Eur Urol Focus. 2019 Jul;5(4):642-649. doi: 10.1016/j.euf.2017.09.008. Epub 2017 Sep 24.
Mutations in the promoter region of the TERT gene have been detected in a variety of cancers. These mutations can potentially lead to unlimited cell divisions and result in poor clinical prognosis.
To determine the role and relevance of TERT promoter region mutations in both clear cell (ccRCC) and non-clear cell (nccRCC) renal cell carcinoma using ultra-deep and whole-genome sequencing methods on primary tumor samples.
DESIGN, SETTING, AND PARTICIPANTS: DNA from 281 kidney tumors (147 ccRCC and 134 nccRCC) was sequenced between 2013 and 2015, and clinical outcomes for these patients from a single institution were retrospectively analyzed.
Differences in patient characteristics and mutational status were tested using Fisher's exact test for categorical variables and the Wilcoxon rank sum test for continuous variables. Survival times were estimated using the Kaplan-Meier method and differences were tested using the log-rank test.
TERT mutations occurred in 12.2% of ccRCC and 10.4% of nccRCC cases. In >80% of the cases, mutations were located at C228T and were found to co-occur only rarely with other relevant RCC driver genes. The median follow-up among survivors overall was 2.5 yr (range 0.1-18.3). TERT promoter mutations were significantly associated with cancer-specific survival in ccRCC (hazard ratio 2.68, 95% confidence interval 1.19-6.01; p=0.013). In nccRCC, TERT mutations were significantly associated with larger tumors and metastatic development. Assessment of further relevant clinical associations was precluded in the nccRCC group by the heterogeneous and small sample size.
Our data suggests that TERT mutational status reflects a distinct pathogenesis with an aggressive disease course in RCC. Stratifying patients with this unique tumorigenesis that leads to poor clinical outcomes could be a putative target for novel therapeutics.
We show a previously unrecognized frequency of TERT promoter mutations in both clear cell and non-clear cell renal cell carcinoma. TERT promoter mutations were associated with some worse outcomes in patients with clear cell renal cell carcinoma.
在各种癌症中都检测到 TERT 基因启动子区域的突变。这些突变可能导致无限的细胞分裂,并导致不良的临床预后。
使用超深度和全基因组测序方法在原发性肿瘤样本中确定 TERT 启动子区域突变在透明细胞(ccRCC)和非透明细胞(nccRCC)肾细胞癌中的作用和相关性。
设计、设置和参与者:2013 年至 2015 年间对 281 例肾肿瘤(147 例 ccRCC 和 134 例 nccRCC)的 DNA 进行了测序,并对来自单一机构的这些患者的临床结果进行了回顾性分析。
使用 Fisher 确切检验对分类变量和 Wilcoxon 秩和检验对连续变量进行检验,以测试患者特征和突变状态的差异。使用 Kaplan-Meier 方法估计生存时间,并使用对数秩检验测试差异。
ccRCC 中 TERT 突变发生率为 12.2%,nccRCC 中为 10.4%。在>80%的病例中,突变位于 C228T,仅很少与其他相关 RCC 驱动基因共同发生。幸存者的中位随访时间为 2.5 年(范围 0.1-18.3)。TERT 启动子突变与 ccRCC 的癌症特异性生存显著相关(风险比 2.68,95%置信区间 1.19-6.01;p=0.013)。在 nccRCC 中,TERT 突变与更大的肿瘤和转移发展显著相关。由于 nccRCC 组的异质性和样本量小,进一步评估相关临床相关性受到限制。
我们的数据表明,TERT 突变状态反映了 RCC 中一种具有侵袭性疾病过程的独特发病机制。对导致不良临床结局的这种独特肿瘤发生进行分层可能是一种新的治疗靶点。
我们显示了 TERT 启动子突变在透明细胞和非透明细胞肾细胞癌中以前未被认识到的频率。TERT 启动子突变与透明细胞肾细胞癌患者的某些较差结局相关。