Molecular Oncology Group of Biodonostia Research Institute, San Sebastian, Spain; IKERBASQUE, Basque Foundation for Science, Bilbao, Spain; Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom.
Molecular Oncology Group of Biodonostia Research Institute, San Sebastian, Spain.
J Mol Diagn. 2018 Jan;20(1):34-45. doi: 10.1016/j.jmoldx.2017.09.002. Epub 2017 Oct 19.
Tubulocystic renal cell carcinoma (TC-RCC) is a rare recently described renal neoplasm characterized by gross, microscopic, and immunohistochemical differences from other renal tumor types and was recently classified as a distinct entity. However, this distinction remains controversial particularly because some genetic studies suggest a close relationship with papillary RCC (PRCC). The molecular basis of this disease remains largely unexplored. We therefore performed noncoding (nc) RNA/miRNA expression analysis and targeted next-generation sequencing mutational profiling on 13 TC-RCC cases (11 pure, two mixed TC-RCC/PRCC) and compared with other renal neoplasms. The expression profile of miRNAs and other ncRNAs in TC-RCC was distinct and validated 10 differentially expressed miRNAs by quantitative RT-PCR, including miR-155 and miR-34a, that were significantly down-regulated compared with PRCC cases (n = 22). With the use of targeted next-generation sequencing we identified mutations in 14 different genes, most frequently (>60% of TC-RCC cases) in ABL1 and PDFGRA genes. These mutations were present in <5% of clear cell RCC, PRCC, or chromophobe RCC cases (n > 600) of The Cancer Genome Atlas database. In summary, this study is by far the largest molecular study of TC-RCC cases and the first to investigate either ncRNA expression or their genomic profile. These results add molecular evidence that TC-RCC is indeed a distinct entity from PRCC and other renal neoplasms.
管状囊性肾细胞癌(TC-RCC)是一种罕见的最近描述的肾肿瘤,其在大体、显微镜和免疫组织化学方面与其他肾肿瘤类型存在差异,最近被分类为一种独特的实体。然而,这种区别仍然存在争议,特别是因为一些遗传研究表明它与乳头状肾细胞癌(PRCC)密切相关。这种疾病的分子基础在很大程度上仍未得到探索。因此,我们对 13 例 TC-RCC 病例(11 例纯型,2 例 TC-RCC/PRCC 混合型)进行了非编码(nc)RNA/miRNA 表达分析和靶向下一代测序突变分析,并与其他肾肿瘤进行了比较。TC-RCC 中 miRNA 和其他 ncRNA 的表达谱是独特的,并通过定量 RT-PCR 验证了 10 个差异表达的 miRNA,包括 miR-155 和 miR-34a,与 PRCC 病例相比明显下调(n=22)。使用靶向下一代测序,我们在 14 个不同基因中鉴定出突变,在 ABL1 和 PDFGRA 基因中最常见(>60%的 TC-RCC 病例)。这些突变在透明细胞肾细胞癌、PRCC 或嗜铬细胞瘤肾细胞癌(n>600)的癌症基因组图谱数据库中不到 5%。总之,这项研究是迄今为止对 TC-RCC 病例进行的最大分子研究,也是第一个调查 ncRNA 表达或其基因组谱的研究。这些结果提供了分子证据,表明 TC-RCC 确实是与 PRCC 和其他肾肿瘤不同的实体。