| Literature DB >> 27783335 |
Estelle Jamard1, Bertrand Volard1, Audrey Emmanuelle Dugué2, Angelina Legros1, Alexandra Leconte2, Bénédicte Clarisse2, Grégoire Davy1, Florence Polycarpe3, Catherine Dugast4,5, Caroline Abadie4,5, Thierry Frebourg6,7, Julie Tinat6,7, Isabelle Tennevet8, Valérie Layet9, Florence Joly2,10,11,12, Laurent Castéra1,6, Pascaline Berthet6,3, Dominique Vaur1,6, Sophie Krieger13,14,15.
Abstract
Germline allele specific expression (ASE), resulting in a lowered expression of one of the BRCA1 alleles, has been described as a possible predisposition marker in Hereditary Breast or Ovarian Cancer (HBOC), usable for molecular diagnosis in HBOC. The main objective of this prospective case-control study was to compare the proportion of ASE between controls without familial history of breast or ovarian cancer, and HBOC cases without BRCA1 or BRCA2 deleterious mutation. BRCA1 ASE evaluated on three SNPs among controls and HBOC patients without deleterious mutation were assessed by pyrosequencing. The allelic ratios and the proportion of ASE were compared between controls and cases using a Student's t test and a Fisher exact test, respectively. The linearity and reproducibility of the ASE dosage was demonstrated with R2 > 0.99 and a coefficient of variation below 10 %, and ASE was detected in two positive controls harbouring BRCA1 truncated mutations. In the heterozygote population, composed of 99/264 controls (37.5 %) and 96/227 patients (42.3 %), we detected a 5 % ASE without truncated mutations, in each population. We failed to detect any significant difference of ASE between controls and patients. So far, BRCA1 Allelic specific expression is not usable in routine diagnosis as a possible predisposition marker in HBOC patients except for the detection of truncated mutations.Entities:
Keywords: Allele specific expression; BRCA1; Breast; Cancer; Ovarian
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Year: 2017 PMID: 27783335 DOI: 10.1007/s10689-016-9940-2
Source DB: PubMed Journal: Fam Cancer ISSN: 1389-9600 Impact factor: 2.375