Multimodal analysis of a rare BARD1 missense variant suggests its pathogenicity is conditional

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Authors: Fiona Chan‐Pak‐Choon, Yuandi Gao, José Camacho Valenzuela, Júlia-Jié Cabré-Romans, Amisha Minju-OP, Lili Fu, Paz P Polak, Bárbara Rivera, Raquel Cuella-Martin, William David Foulkes
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References: 45

Abstract

Hereditary breast cancer involves multiple risk genes, including BARD1, which confers low to moderate risk and is associated with triple-negative breast cancer (TNBC). We report a proband with a primary ER+/PR+/HER2- breast cancer, which recurred unilaterally as a TNBC and who later developed endometrial cancer. Clinical germline testing revealed a rare BARD1 missense variant of uncertain significance [c.2258G>T; p.(Gly753Val)]. Whole-exome sequencing of tumors and blood revealed BARD1 loss of heterozygosity and mutational signature 3 - indicative of homologous recombination (HR) repair deficiency - exclusively in the TNBC recurrence. Functional assays demonstrated impaired HR repair via increased PARP inhibitor sensitivity and reduced RAD51 foci formation. We hypothesize that the selective pressure exerted by tamoxifen resulted in breast cancer subtype switching and uncovered the pathogenic potential of the BARD1 p.(Gly753Val) variant. This case illustrates a previously unreported scenario where the pathogenicity of a germline BARD1 variant appears conditional on prior treatment.

Fields of Study & Subjects

Cancer Genomics and Diagnostics Genomics and Rare Diseases RNA modifications and cancer

Publication details

Journal / source
npj Breast Cancer
Publisher
Springer Science and Business Media LLC
Volume
12
Issue
1
Publication date
21 April 2026
Language
EN