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. (19th December 2020)

• Record Type: Journal Article
• Authors: 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
• Is Part Of: Journal of oral pathology & medicine. Volume 50:Number 4(2021)
• Page Start: 410
• Page End: 417
• Publication Date: 2020-12-19
• Subjects: genetics -- lysosomes -- oral granular cell tumor -- soft tissue neoplasms -- V‐ATPase; Dentistry -- Periodicals; Teeth -- Diseases -- Periodicals; 617
• DOI: 10.1111/jop.13148
• Languages: English
• ISSNs: 0904-2512

Abstract

Abstract: 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.