| Literature DB >> 29084058 |
Fredrik Petersson1, Petr Martinek2, Tomas Vanecek2, Kristyna Pivovarcikova2, Kvetoslava Peckova2, Ondrej Ondic2, Delia Perez-Montiel3, Faruk Skenderi4, Monika Ulamec5, Rudolf Nenutil6, Milan Hora7, Tomas Svoboda8, Pavla Rotterova2, Martin Dusek2, Michal Michal2, Ondrej Hes2.
Abstract
We have studied a cohort of renal cell carcinomas (RCCs) with smooth-muscle stroma (N=6), which lacked any of following genetic aberrations: mutations in the VHL-gene-coding sequence, loss of heterozygosity of chromosome 3p, or hypermethylation of VHL. Using targeted next-generation sequencing, no intronic VHL mutations or mutations in selected genes involved in angiogenesis and genes frequently mutated in clear cell RCC were identified. Tumors were also tested for the presence of hotspot mutations in the TCEB1 gene with negative results in all cases. We conclude that there exists a group of RCCs with abundant leiomyomatous stroma, where the epithelial component is indistinguishable from conventional clear cell RCC and distinct from clear cell (tubulo-) papillary RCC and that these tumors lack aberrations related to the function of the VHL gene, mutations in genes involved in angiogenesis, and hotspot mutations in the TCEB1 gene.Entities:
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Year: 2018 PMID: 29084058 DOI: 10.1097/PAI.0000000000000410
Source DB: PubMed Journal: Appl Immunohistochem Mol Morphol ISSN: 1533-4058