KANK1-NTRK3 fusions define a subset of BRAF mutation negative renal metanephric adenomas
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články
PubMed
33046021
PubMed Central
PMC7552490
DOI
10.1186/s12881-020-01143-6
PII: 10.1186/s12881-020-01143-6
Knihovny.cz E-zdroje
- Klíčová slova
- BRAFV600E, Chromosomal translocations, Cytogenetics, KANK1-NTRK3 fusion, Metanephric adenoma,
- MeSH
- adaptorové proteiny signální transdukční genetika MeSH
- adenom genetika patologie MeSH
- cytoskeletální proteiny genetika MeSH
- dítě MeSH
- dospělí MeSH
- fúzní onkogenní proteiny genetika MeSH
- hybridizace in situ fluorescenční MeSH
- lidé středního věku MeSH
- lidé MeSH
- lidské chromozomy, pár 15 genetika MeSH
- lidské chromozomy, pár 9 genetika MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mutace * MeSH
- nádory ledvin genetika patologie MeSH
- protoonkogenní proteiny B-Raf genetika MeSH
- receptor trkC genetika MeSH
- senioři MeSH
- translokace genetická MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- adaptorové proteiny signální transdukční MeSH
- cytoskeletální proteiny MeSH
- fúzní onkogenní proteiny MeSH
- KANK1 protein, human MeSH Prohlížeč
- NTRK3 protein, human MeSH Prohlížeč
- protoonkogenní proteiny B-Raf MeSH
- receptor trkC MeSH
BACKGROUND: Metanephric adenoma (MA) is a rare benign renal neoplasm. On occasion, MA can be difficult to differentiate from renal malignancies such as papillary renal cell carcinoma in adults and Wilms̕ tumor in children. Despite recent advancements in tumor genomics, there is limited data available regarding the genetic alterations characteristic of MA. The purpose of this study is to determine the frequency of metanephric adenoma cases exhibiting cytogenetic aberration t (9;15)(p24;q24), and to investigate the association between t (9,15) and BRAF mutation in metanephric adenoma. METHODS: This study was conducted on 28 archival formalin fixed paraffin-embedded (FFPE) specimens from patients with pathologically confirmed MA. Tissue blocks were selected for BRAF sequencing and fluorescent in situ hybridization (FISH) analysis for chromosomal rearrangement between KANK1 on chromosome 9 (9p24.3) and NTRK3 on chromosome 15 (15q25.3), which was previously characterized and described in two MA cases. RESULTS: BRAFV600E mutation was identified in 62% of our cases, 9 (38%) cases were BRAFWT, and 4 cases were uninformative. Of the 20 tumors with FISH results, two (10%) were positive for KANK1-NTRK3 fusion. Both cases were BRAFWT suggesting mutual exclusivity of BRAFV600E and KANK1-NTRK3 fusion, the first such observation in the literature. CONCLUSIONS: Our data shows that BRAF mutation in MA may not be as frequent as suggested in the literature and KANK-NTRK3 fusions may account for a subset of BRAFWT cases in younger patients. FISH analysis for KANK1-NTRK3 fusion or conventional cytogenetic analysis may be warranted to establish the diagnosis of MA in morphologically and immunohistochemically ambiguous MA cases lacking BRAF mutations.
Advocate Medical Group Genetics Park Ridge IL USA
Department of Cytogenetics ACL Laboratories Rosemont IL USA
Department of Pathology Advocate Lutheran General Hospital Park Ridge IL USA
Department of Pathology and Pediatrics University of Texas Southwestern Medical Center Dallas TX USA
Department of Pathology Charles University Hospital Pilsen Pilsen Czech Republic
Department of Pathology Saint Joseph Hospital Denver CO USA
Departments of Pathology and Laboratory Medicine Children's Health Dallas TX USA
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