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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
Author(s) -
França Josiane Alves,
Gayden Tenzin,
Bareke Eric,
Santos Jean Nunes,
Sousa Sílvia Ferreira,
BastosRodrigues Luciana,
Majewski Jacek,
Jabado Nada,
Gomez Ricardo Santiago,
Gomes Carolina Cavalieri
Publication year - 2021
Publication title -
journal of oral pathology and medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.887
H-Index - 83
eISSN - 1600-0714
pISSN - 0904-2512
DOI - 10.1111/jop.13148
Subject(s) - biology , exome sequencing , gene , endosome , exome , pathology , microbiology and biotechnology , mutation , cell , genetics , medicine
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.