# BRCA1 and BRCA2 as prognostic markers in oral squamous cell carcinoma: a minireview

**Authors:** Dominika Gedeonová, Claretta Bianchi, Jan Štembírek, Matouš Hrdinka, Zuzana Chyra, Marcela Buchtová, Pavel Hurník, Tomáš Blažek, Jana Režnarová

PMC · DOI: 10.3389/fonc.2025.1528822 · Frontiers in Oncology · 2025-03-28

## TL;DR

This review discusses how BRCA1 and BRCA2 genes, known for breast and ovarian cancer, may also serve as important markers in oral squamous cell carcinoma.

## Contribution

The paper highlights the novel potential of BRCA1 and BRCA2 as prognostic and therapeutic biomarkers in oral squamous cell carcinoma.

## Key findings

- BRCA1 and BRCA2 genes are involved in DNA repair and may influence chemotherapy resistance in OSCC.
- Despite low mutation prevalence in OSCC, BRCA genes could still serve as clinical biomarkers for personalized treatment.
- More standardized studies are needed to confirm the clinical utility of BRCA genes in OSCC management.

## Abstract

Oral squamous cell carcinoma (OSCC), a subset of head and neck cancers, primarily originates in the epithelial tissues of the oral cavity. Despite advancements in treatment, the mortality rate for OSCC remains around 50%, underscoring the urgent need for improved prognostic markers. This review explores the role of the BRCA1 and BRCA2 genes—traditionally associated with breast and ovarian cancers—in the context of OSCC. We discuss the molecular pathways involving BRCA genes, their potential as diagnostics and prognostic biomarkers, and their implications for personalized treatment strategies, including addressing chemotherapy resistance. Furthermore, this review emphasizes the significance of genome stability in cancer progression and examines both current and emerging methodologies for detecting BRCA mutations in OSCC patients. Despite limited prevalence of BRCA mutations in OSCC compared to other cancers, their role in DNA repair and therapeutic response underscores their potential as clinical biomarkers. However, standardized, multicenter studies are still needed to validate their utility in OSCC management. A better understanding of the role of BRCA genes in OSCC could pave the way for more effective therapeutic approaches and improved patient outcomes.

## Linked entities

- **Genes:** BRCA1 (BRCA1 DNA repair associated) [NCBI Gene 672], BRCA2 (BRCA2 DNA repair associated) [NCBI Gene 675]
- **Diseases:** oral squamous cell carcinoma (MONDO:0004958), breast cancer (MONDO:0004989), ovarian cancer (MONDO:0005140)

## Full-text entities

- **Genes:** BRCA2 (BRCA2 DNA repair associated) [NCBI Gene 675] {aka BRCC2, BROVCA2, FACD, FAD, FAD1, FANCD}, BRCA1 (BRCA1 DNA repair associated) [NCBI Gene 672] {aka BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4}
- **Diseases:** head and neck cancers (MESH:D006258), breast and ovarian cancers (MESH:D061325), OSCC (MESH:D000077195), cancer (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11986421/full.md

## References

75 references — full list in the complete paper: https://tomesphere.com/paper/PMC11986421/full.md

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Source: https://tomesphere.com/paper/PMC11986421