Prognostic significance of 1p36 locus deletion in adenoid cystic carcinoma of the salivary glands
Language English Country Germany Media print-electronic
Document type Journal Article
Grant support
SVV-2017-260 391
Ministerstvo Školství, Mládeže a Tělovýchovy
PubMed
29619555
DOI
10.1007/s00428-018-2349-6
PII: 10.1007/s00428-018-2349-6
Knihovny.cz E-resources
- Keywords
- 1p36 locus deletion, Adenoid cystic carcinoma, MYB-NFIB, Prognosis, Salivary gland,
- MeSH
- Carcinoma, Adenoid Cystic genetics mortality secondary therapy MeSH
- Time Factors MeSH
- Chromosome Deletion * MeSH
- Adult MeSH
- Phenotype MeSH
- Gene Fusion MeSH
- Oncogene Proteins, Fusion genetics MeSH
- Genetic Predisposition to Disease MeSH
- In Situ Hybridization, Fluorescence MeSH
- Immunohistochemistry MeSH
- Kaplan-Meier Estimate MeSH
- Middle Aged MeSH
- Humans MeSH
- Chromosomes, Human, Pair 1 * MeSH
- Neoplasm Recurrence, Local MeSH
- Adolescent MeSH
- Young Adult MeSH
- Biomarkers, Tumor genetics MeSH
- Salivary Gland Neoplasms genetics mortality pathology therapy MeSH
- Disease-Free Survival MeSH
- Disease Progression MeSH
- Proportional Hazards Models MeSH
- Proto-Oncogene Proteins genetics MeSH
- Risk Factors MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Neoplasm Staging MeSH
- Neoplasm Grading MeSH
- Trans-Activators genetics MeSH
- NFI Transcription Factors genetics MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Oncogene Proteins, Fusion MeSH
- MYB-NFIB fusion protein, human MeSH Browser
- MYBL1 protein, human MeSH Browser
- Biomarkers, Tumor MeSH
- NFIB protein, human MeSH Browser
- Proto-Oncogene Proteins MeSH
- Trans-Activators MeSH
- NFI Transcription Factors MeSH
Adenoid cystic carcinoma (AdCC) of the salivary glands is characterized by MYB-NFIB or MYBL1-NFIB fusion, prolonged but relentlessly progressive clinical course with frequent recurrences, and development of distant metastasis resulting in high long-term mortality. Currently, no effective therapy is available for patients with advanced non-resectable and/or metastatic disease. Complicating the clinical management of this patient group is the lack of prognostic markers. The purpose of this study is to investigate the prognostic value of 1p36 loss in patients with AdCC. The presence of 1p36 deletion and gene fusions involving the MYB, NFIB, and MYBL1 genes in a cohort of 93 salivary gland AdCCs was studied using fluorescence in situ hybridization. These results were statistically correlated with clinical data and outcome. Deletion of 1p36 in AdCC was identified in 13 of 85 analyzable cases (15.29%). MYB-NFIB fusion was detected in 57/85 (67.1%), MYBL1-NFIB fusion in 12/85 (14.1%), MYB-X fusion in 4/85 (4.7%), MYBL1-X in 4/85 (4.7%), and NFIB-X in 2/85 (2.4%) of AdCC cases. None of the 1p36-deleted samples showed MYBL1 rearrangement. Statistical analysis demonstrated a significant correlation between 1p36 deletion and advanced tumor stage and solid histology (p = 0.0061 and 0.0007, respectively). Kaplan-Meier survival curves showed statistically significant correlations between 1p36 deletion and decreased overall survival, disease-specific survival, recurrence-free interval, and recurrence-free survival, all of which were maintained in multivariate analysis. We demonstrate that 1p36 deletion can serve as an indicator of unfavorable outcome of patients with salivary gland AdCC.
Department of Oral Pathology Faculty of Dentistry University of São Paulo São Paulo Brazil
Department of Otorhinolaryngology and Maxillofacial Surgery Zealand University Hospital Køge Denmark
Department of Pathology Faculty of Medicine in Plzen Charles University Plzen Czech Republic
Department of Pathology Rigshospitalet Copenhagen University Hospital Copenhagen Denmark
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