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Hereditary cancer predisposition due to variation(s) in the BRCA1 gene. Germline pathogenic or likely pathogenic variants in the BRCA1 gene confer an autosomal dominant predisposition to hereditary breast and ovarian cancer. Tumor formation at other sites, including pancreatic cancer have been described.
Biomarker and diagnostic research for BRCA1-related cancer predisposition has been reported in the published literature.
No clinical trials have been registered for BRCA1-related cancer predisposition.
5 publications have been identified in PubMed for BRCA1-related cancer predisposition. Research spans Diagnostic / Biomarker (40%), Review / Meta-Analysis (40%), and Basic Science / Preclinical (20%).
Sasagawa H (2026). [PMID: 41423785](https://pubmed.ncbi.nlm.nih.gov/41423785/). *JNCI cancer spectrum*. [Diagnostic / Biomarker]
Jurgiel WA (2026). [PMID: 41538105](https://pubmed.ncbi.nlm.nih.gov/41538105/). *Discover oncology*. [Review / Meta-Analysis]
Yu M (2026). [PMID: 41247621](https://pubmed.ncbi.nlm.nih.gov/41247621/). *Genes & genomics*. [Review / Meta-Analysis]
Palleschi M (2025). [PMID: 40338220](https://pubmed.ncbi.nlm.nih.gov/40338220/). *The oncologist*. [Basic Science / Preclinical]
Nakahara M (2024). [PMID: 39077936](https://pubmed.ncbi.nlm.nih.gov/39077936/). *The journal of obstetrics and gynaecology research*. [Diagnostic / Biomarker]
Data assembled from 2 of 12 sources · Last updated Sep 18, 2026, 4:35 PM UTC
Common questions about BRCA1-related cancer predisposition
AI-curated news mentioning BRCA1-related cancer predisposition
Updated Jul 8, 2026
A new treatment for children aged 2 or older with sickle cell disease has been approved by the U.S. Food & Drug Administration. In a press release on Wednesday, the FDA announced it had approved Casgevy, the first gene therapy for children with sickle cell disease. (NewsNation) — A new treatment for children aged 2 or older with sickle cell disease has been approved by the Food & Drug Administration (FDA). In a Wednesday news release, the FDA announced it had approved Casgevy, the first gene therapy for children with the disease. “Casgevy is a gene therapy consisting of the patient’s own (autologous) hematopoietic (blood) stem cells, administered as a one-time single dose for intravenous infusion,” the release noted. “Pediatric patients as young as 2 years of age can now access a critical additional treatment option to treat these debilitating, life-threatening diseases,” Karim Mikhail, the acting director of the Center for Biologics Evaluation and Research, wrote. “These disorders carry a heavy burden for children and their families, affecting growth, development, and long-term health in profound ways,” Megha Kaushal, acting deputy director of the Office of Therapeutic Products in CBER, said in the release.