Petersson Fredrik, Martinek Petr, Vanecek Tomas, Pivovarcikova Kristyna, Peckova Kvetoslava, Ondic Ondrej, Perez-Montiel Delia, Skenderi Faruk, Ulamec Monika, Nenutil Rudolf, Hora Milan, Svoboda Tomas, Rotterova Pavla, Dusek Martin, Michal Michal, Hes Ondrej
Department of Pathology, National University Health System Hospital, Singapore, Singapore.
Departments of Pathology.
Appl Immunohistochem Mol Morphol. 2018 Mar;26(3):192-197. doi: 10.1097/PAI.0000000000000410.
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.
我们研究了一组具有平滑肌基质的肾细胞癌(RCC,n = 6),这些肿瘤不存在以下任何一种基因异常:VHL基因编码序列突变、3号染色体短臂杂合性缺失或VHL高甲基化。通过靶向二代测序,未发现内含子VHL突变或血管生成相关所选基因以及透明细胞RCC中常见突变基因的突变。还检测了肿瘤中TCEB1基因热点突变的存在情况,所有病例结果均为阴性。我们得出结论,存在一组具有丰富平滑肌瘤样基质的RCC,其上皮成分与传统透明细胞RCC难以区分,且与透明细胞(小管状)乳头状RCC不同,并且这些肿瘤缺乏与VHL基因功能相关的异常、血管生成相关基因的突变以及TCEB1基因的热点突变。