
Faculty, Staff and Student Publications
Publication Date
12-1-2022
Journal
European Academy of Dermatology and Venereology
Abstract
Background: Kaposi sarcoma (KS) is a rare skin tumour caused by herpesvirus 8 infection and characterized by either indolence or an aggressive course necessitating systemic therapies. The genetic basis of this difference remains unknown.
Objectives: To explore the tumour mutational burden in indolent and aggressive KS.
Methods: We performed whole-exome sequencing on a cohort of 21 KS patients. We compared genetic landscape including tumor mutational burden between the two forms of indolent and agressive KS.
Results: Aggressive KS tumours had a significantly higher TMB and a larger cumulative number of deleterious mutations than indolent KS tumours. In addition, all aggressive tumours had at least three deleterious mutations, whereas most indolent tumours harboured only one or no predicted deleterious mutations. Deleterious mutations listed in the Cancer Gene Census were detected exclusively in patients with aggressive disease. An analysis of somatic copy-number alterations (SCNA) revealed a tendency towards higher number of alterations in aggressive KS.
Conclusions: These data suggest that SCNA alterations and an increase in mutational burden promote aggressive KS and that it might be more appropriate to consider indolent KS as an opportunistic skin disease rather than a cancer.
Keywords
Humans, Sarcoma, Kaposi, Herpesvirus 8, Human, Acquired Immunodeficiency Syndrome, Skin Neoplasms, Mutation
DOI
10.1111/jdv.18463
PMID
35881110
PMCID
PMC11803637
PubMedCentral® Posted Date
2-7-2025
PubMedCentral® Full Text Version
Author MSS
Published Open-Access
yes
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