Whole-exome sequencing identifies distinct genomic aberrations in eccrine porocarcinomas and poromas
EPCs and EPs are generally heterogeneous tumor entities with a few distinct discrepancies from each other. The findings from this study emphasize the need to further verify the roles of disrupted genes and pathways in the initiation and progression of EPCs and EPs.
Authors
- Harri Sihto (ORCID: https://orcid.org/0000-0001-5265-5509)
- Maya Puttonen (ORCID: https://orcid.org/0009-0002-3982-9038)
- Henrikki Almusa
- Tom Böhling (ORCID: https://orcid.org/0000-0001-8903-3690)
- Virve Koljonen (ORCID: https://orcid.org/0000-0003-0398-4829)
Institutions
- University of Helsinki (FI)
- Helsinki University Hospital (FI)
- Institute for Molecular Medicine Finland (FI)
Publication Details
- Journal
- Orphanet Journal of Rare Diseases
- Published
- 2025-02-13
- DOI
- https://doi.org/10.1186/s13023-025-03586-7
- Citations
- 3
- Primary Topic
- Cancer and Skin Lesions
- Type
- article
- Field-Weighted Citation Impact
- 6.01
Funders
- Helsingin Yliopisto
- Helsingin ja Uudenmaan Sairaanhoitopiiri
- Medicinska Understödsföreningen Liv och Hälsa
- Finska Läkaresällskapet
- Jane ja Aatos Erkon Säätiö
- Emil Aaltosen Säätiö
- Syöpäsäätiö