BRCA1 secondary splice-site mutations
BRCA1 splice isoforms d11 and d11q can contribute to PARP inhibitor (PARPi) resistance by splicing-out mutation-containing exons, producing truncated, partially-functional proteins. However, the clinical impact and underlying drivers of BRCA1 exon skipping remain undetermined. We analyzed nine ovarian and breast cancer patient derived xenografts (PDX) with BRCA1 exon 11 frameshift mutations for splice isoform expression and therapy response.
- Type: Cancer Genomics
- Archiver: European Genome-Phenome Archive (EGA)
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
Dataset ID | Description | Technology | Samples |
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EGAD50000000032 | Illumina NovaSeq 6000 | 5 | |
EGAD50000000033 | Illumina NovaSeq 6000 | 5 | |
EGAD50000000034 | NextSeq 500 | 4 | |
EGAD50000000035 | Illumina HiSeq 2500 Illumina NovaSeq 6000 | 15 | |
EGAD50000000189 | Illumina NovaSeq 6000 | 2 |
Publications | Citations |
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BRCA1 secondary splice-site mutations drive exon-skipping and PARP inhibitor resistance.
Mol Cancer 23: 2024 158 |
1 |