Journal article
Desmosome mutations impact the tumor microenvironment to promote melanoma proliferation
- Abstract:
- Desmosomes are transmembrane protein complexes that contribute to cell–cell adhesion in epithelia and other tissues. Here, we report the discovery of frequent genetic alterations in the desmosome in human cancers, with the strongest signal seen in cutaneous melanoma, where desmosomes are mutated in more than 70% of cases. In primary but not metastatic melanoma biopsies, the burden of coding mutations in desmosome genes is associated with a strong reduction in desmosome gene expression. Analysis by spatial transcriptomics and protein immunofluorescence suggests that these decreases in expression occur in keratinocytes in the microenvironment rather than in primary melanoma cells. In further support of a microenvironmental origin, we find that desmosome gene knockdown in keratinocytes yields markedly increased proliferation of adjacent melanoma cells in keratinocyte and melanoma cocultures. Similar increases in melanoma proliferation are observed in media preconditioned with desmosome-deficient keratinocytes. Thus, gradual accumulation of desmosome mutations in neighboring cells may prime melanoma cells for neoplastic transformation.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
-
-
(Preview, Accepted manuscript, pdf, 5.5MB, Terms of use)
-
- Publisher copy:
- 10.1038/s41588-025-02163-9
Authors
- Publisher:
- Springer Nature
- Journal:
- Nature Genetics More from this journal
- Volume:
- 57
- Issue:
- 5
- Pages:
- 1179-1188
- Publication date:
- 2025-04-16
- Acceptance date:
- 2025-03-12
- DOI:
- EISSN:
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1546-1718
- ISSN:
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1061-4036
- Pmid:
-
40240879
- Language:
-
English
- Keywords:
- Pubs id:
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2119755
- Local pid:
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pubs:2119755
- Deposit date:
-
2025-07-18
Terms of use
- Copyright holder:
- Baron et al.
- Copyright date:
- 2025
- Rights statement:
- Copyright © 2025, The Author(s), under exclusive licence to Springer Nature America, Inc.
- Notes:
- The author accepted manuscript (AAM) of this paper has been made available under the University of Oxford's Open Access Publications Policy, and a CC BY public copyright licence has been applied.
- Licence:
- CC Attribution (CC BY)
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