Identifying the BRCA1 c.-107A > T variant in Dutch patients with a tumor BRCA1 promoter hypermethylation

Abstract An inherited single nucleotide variant (SNV) in the 5′UTR of the BRCA1 gene c.-107A > T was identified to be related to BRCA1 promoter hypermethylation and a hereditary breast and ovarian cancer phenotype in two UK families. We investigated whether this BRCA1 variant was also present in a Dutch cohort of breast and ovarian cancer patients with tumor BRCA1 promoter hypermethylation. We selected all breast and ovarian cancer cases that tested positive for tumor BRCA1 promoter hypermethylation at the Netherlands Cancer Institute and Sanger sequenced the specific mutation in the tumor... Mehr ...

Verfasser: de Jong, Vincent M. T.
Pruntel, Roelof
Steenbruggen, Tessa G.
Bleeker, Fonnet E.
Nederlof, Petra
Hogervorst, Frans B. L.
linn, Sabine C.
Dokumenttyp: Artikel
Erscheinungsdatum: 2022
Reihe/Periodikum: Familial Cancer ; volume 22, issue 2, page 151-154 ; ISSN 1389-9600 1573-7292
Verlag/Hrsg.: Springer Science and Business Media LLC
Schlagwörter: Cancer Research / Genetics (clinical) / Oncology / Genetics
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26678536
Datenquelle: BASE; Originalkatalog
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Link(s) : http://dx.doi.org/10.1007/s10689-022-00314-z