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Clinical, histological, and molecular differences in melanoma due to different TERT promoter mutations subtypes. A retrospective cross-sectional study in 684 melanoma patients
E. Manrique-Silva, ME. David, AM. Maider, Z. García-Casado, R. Moro, C. Requena, V. Través, A. Virós, R. Kumar, E. Nagore
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
PPRC-2018-36 of the European Academy of Dermatology and Venereology (EADV)
Asociación Española Contra el Cáncer-Valencia (AECC, "Ayudas predoctorales en oncología" grant)
PubMed
38153178
DOI
10.1111/pcmr.13155
Knihovny.cz E-zdroje
- MeSH
- lidé MeSH
- melanom * genetika patologie mortalita MeSH
- mutace MeSH
- nádory kůže genetika patologie mortalita MeSH
- promotorové oblasti (genetika) * genetika MeSH
- průřezové studie MeSH
- retrospektivní studie MeSH
- telomerasa * genetika MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Differences in survival according to the pTERT mutation subtypes (-124C > T, -146C > T, and tandem -138_139CC > TT) have been observed. The present study aimed to describe the clinical as the histopathological and molecular cutaneous melanoma features according to the presence of the three most prevalent pTERT mutation subtypes (-124C > T, -146C > T, and tandem -138_139CC > TT). A retrospective cross-sectional study including 684 patients was designed, and a Partial Least-Squares Discriminant Analysis (PLS-DA) was performed. After the PSL-DA, it was observed that the tandem -138_139CC > TT subtype differs from the other subtypes. The model demonstrated that the -124C > T and the -138_139 CC > TT subtypes were associated with fast-growing melanomas (OR 0.5, CI 0.29-0.86, p = .012) and with Breslow >2 mm (OR 0.6, CI 0.37-0.97, p = .037), compared to the -146C > T mutation. Finally, the -124C > T appeared to be more associated with the presence of TILs (non-brisk) than the -146C > T (OR 0.6, CI 0.40-1.01, p = .05). These findings confirmed that the -124C > T and the tandem -138_139 CC > TT subtypes are both highly associated with the presence of features of aggressiveness; however, only the -124C > T was highly associated with TILs. This difference could explain the worse survival rate associated with the tandem -138_139CC > TT mutations.
Department of Dermatology Fundación Instituto Valenciano de Oncología Valencia Spain
Department of Pathological Anatomy Fundación Instituto Valenciano de Oncología Valencia Spain
Division of Functional Genome Analysis Deutsches Krebsforschüngzentrum Heidelberg Germany
Escuela de Doctorado Universidad Católica de Valencia San Vicente Mártir València Spain
Institute of Medical Biometry and Informatics University of Heidelberg Heidelberg Germany
Instituto Dermatológico Dr Alonso Hospital Vithas Valencia 9 de Octubre Spain
Laboratory of Molecular Biology Fundación Instituto Valenciano de Oncología Valencia Spain
School of Medicine Universidad Católica de Valencia San Vicente Mártir València Spain
Citace poskytuje Crossref.org
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