Germline mutations in cancer susceptibility genes in high grade serous ovarian cancer in Serbia.
Adult
Aged
BRCA1 Protein
/ genetics
BRCA2 Protein
/ genetics
Cell Cycle Proteins
/ genetics
Checkpoint Kinase 2
/ genetics
DNA-Binding Proteins
/ genetics
Fanconi Anemia Complementation Group Proteins
/ genetics
Female
Genetic Predisposition to Disease
Genetic Testing
Germ-Line Mutation
/ genetics
High-Throughput Nucleotide Sequencing
Humans
Middle Aged
Neoplasm Grading
Nuclear Proteins
/ genetics
Ovarian Neoplasms
/ epidemiology
RNA Helicases
/ genetics
Serbia
/ epidemiology
Journal
Journal of human genetics
ISSN: 1435-232X
Titre abrégé: J Hum Genet
Pays: England
ID NLM: 9808008
Informations de publication
Date de publication:
Apr 2019
Apr 2019
Historique:
received:
07
09
2018
accepted:
03
01
2019
revised:
05
12
2018
pubmed:
18
1
2019
medline:
15
3
2019
entrez:
18
1
2019
Statut:
ppublish
Résumé
Clinical criteria for genetic testing of genes other than BRCA1/2 in epithelial ovarian cancer (EOC) still do not exist. We assessed the frequency and predictors of deleterious mutations in 19 cancer predisposition genes in high-grade serous ovarian cancer (HGSOC) in Serbia. Next-generation sequencing was used to identify germline mutations in the whole coding regions of a gene panel. Patients' characteristics and sequencing data were summarized with descriptive statistics and compared using chi-square test. Among 131 HGSOC patients, 23 had BRCA1 (17.6%) while 5 had BRCA2 (3.8%) mutation. In addition, 9 (6.9%) pathogenic mutations were detected in other genes including BRIP1 (n = 2;1.5%), CHEK2 (n = 2;1.5%), NBN (n = 3;2.3%) and RAD51C (n = 2;1.5%). Factors that predicted for BRCA1/2 mutations were: breast and ovarian cancers in the same patient (p = 0.031), young age of EOC (p = 0.029), menstrual status (p = 0.004) and family history of cancer (p < 0.0001). However, these factors did not predict for mutations in other cancer susceptibility genes. Applying established referral criteria for genetic testing in Serbia will help identify BRCA1/2 mutation carriers but will not help identify mutations in other cancer susceptibility genes. Until better predictors emerge we should be performing wider genetic testing of EOC in order to identify all mutation carriers.
Identifiants
pubmed: 30651582
doi: 10.1038/s10038-019-0562-z
pii: 10.1038/s10038-019-0562-z
doi:
Substances chimiques
BRCA1 Protein
0
BRCA1 protein, human
0
BRCA2 Protein
0
BRCA2 protein, human
0
Cell Cycle Proteins
0
DNA-Binding Proteins
0
Fanconi Anemia Complementation Group Proteins
0
NBN protein, human
0
Nuclear Proteins
0
RAD51C protein, human
0
Checkpoint Kinase 2
EC 2.7.1.11
CHEK2 protein, human
EC 2.7.11.1
BRIP1 protein, human
EC 3.6.4.13
RNA Helicases
EC 3.6.4.13
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
281-290Références
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