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Published on: January 22, 2013
Noncoding RNA Expression and Targeted Next-Generation Sequencing Distinguish Tubulocystic Renal Cell Carcinoma
Charles H Lawrie1, María Armesto2, Marta Fernandez-Mercado2
1Molecular 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.
Abstract:
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.
Insights
Tubulocystic renal cell carcinoma (TC-RCC) is a distinct kidney cancer. Molecular analysis revealed unique noncoding RNA profiles and mutations in ABL1 and PDFGRA genes, differentiating it from papillary renal cell carcinoma (PRCC).
Area of Science:
- Oncology
- Genomics
- Molecular Biology
Background:
- Tubulocystic renal cell carcinoma (TC-RCC) is a rare kidney neoplasm, recently classified as distinct.
- Its classification is debated due to potential links with papillary renal cell carcinoma (PRCC).
- The molecular underpinnings of TC-RCC remain largely uninvestigated.
Purpose of the Study:
- To investigate the molecular characteristics of TC-RCC.
- To compare the noncoding RNA (ncRNA) and genomic profiles of TC-RCC with other renal neoplasms.
- To provide molecular evidence for TC-RCC's distinct entity status.
Main Methods:
- Analysis of ncRNA/microRNA (miRNA) expression in 13 TC-RCC cases.
- Targeted next-generation sequencing for mutational profiling.
- Comparison with data from The Cancer Genome Atlas (TCGA) database for other renal neoplasms.
Main Results:
- TC-RCC exhibited a distinct miRNA and ncRNA expression profile compared to other renal tumors.
- Ten differentially expressed miRNAs were validated, with miR-155 and miR-34a significantly down-regulated versus PRCC.
- Mutations in ABL1 and PDFGRA genes were identified in over 60% of TC-RCC cases, found in less than 5% of other renal neoplasms.
Conclusions:
- This study provides the largest molecular investigation of TC-RCC to date.
- Molecular data, including ncRNA expression and genomic profiling, supports TC-RCC as a distinct entity.
- Findings differentiate TC-RCC from PRCC and other renal neoplasms, aiding in classification and understanding.
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