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Whole-exome sequencing reveals novel vacuolar ATPase genes' variants and variants in genes involved in lysosomal biology and autophagosomal formation in oral granular cell tumors.
França, Josiane Alves; Gayden, Tenzin; Bareke, Eric; Santos, Jean Nunes; de Sousa, Sílvia Ferreira; Bastos-Rodrigues, Luciana; Majewski, Jacek; Jabado, Nada; Gomez, Ricardo Santiago; Gomes, Carolina Cavalieri.
Afiliação
  • França JA; Department of Pathology, Biological Sciences Institute, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
  • Gayden T; Department of Human Genetics, McGill University, Montreal, Canada.
  • Bareke E; Department of Human Genetics, McGill University, Montreal, Canada.
  • Santos JN; McGill Genome Centre, Montreal, Canada.
  • de Sousa SF; Department of Oral Pathology, School of Dentistry, Universidade Federal da Bahia, Salvador, Brazil.
  • Bastos-Rodrigues L; Department of Oral Surgery and Pathology, Faculty of Dentistry, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
  • Majewski J; Department of Nutrition, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
  • Jabado N; Department of Human Genetics, McGill University, Montreal, Canada.
  • Gomez RS; McGill Genome Centre, Montreal, Canada.
  • Gomes CC; Department of Human Genetics, McGill University, Montreal, Canada.
J Oral Pathol Med ; 50(4): 410-417, 2021 Apr.
Article em En | MEDLINE | ID: mdl-33289181
BACKGROUND: Granular cell tumors (GCTs) are rare neuroectodermal soft tissue neoplasms that mainly affect the skin of the upper limbs and trunks and the oral cavity. GCTs are derived from Schwann cells and, ultrastructurally, their intracytoplasmic granules are considered autophagosomes or autophagolysosomes and are consistent with myelin accumulation. METHODS: In this study, a convenience set of 22 formalin-fixed, paraffin-embedded samples of oral GCTs, all but one sample located at the tongue, was screened for mutations by whole-exome (WES) or targeted sequencing. RESULTS: WES revealed two novel variants in genes of the vacuolar ATPase (V-ATPase) complex: ATP6AP1 frameshift c.746_749del, leading to p.P249Hfs*4, and ATP6V1A non-synonymous c.G868A, leading to p.D290N. Each of these mutations occurred in one case. With regard to the samples that were wild type for these V-ATPase variants, at least two samples presented variants in genes that are part of endosomal/lysosomal/autophagosomal networks including ABCA8, ABCC6, AGAP3, ATG9A, CTSB, DNAJC13, GALC, NPC1, SLC15A3, SLC31A2, and TMEM104. CONCLUSION: Although the mechanisms involved in oral GCT initiation and progression remain unclear, our results suggest that oral GCTs have V-ATPase variants similarly to GCTs from other tissues/organs, and additionally show variants in lysosomes/endosomes/autophagosomal genes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tumor de Células Granulares / ATPases Vacuolares Próton-Translocadoras Limite: Humans Idioma: En Revista: J Oral Pathol Med Assunto da revista: ODONTOLOGIA / PATOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil País de publicação: Dinamarca
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tumor de Células Granulares / ATPases Vacuolares Próton-Translocadoras Limite: Humans Idioma: En Revista: J Oral Pathol Med Assunto da revista: ODONTOLOGIA / PATOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil País de publicação: Dinamarca