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February 5, 2026Cancers0 citationsOpen Access

Frequency of Founder Mutations in BRCA1 and BRCA2 Genes in Hereditary Breast Cancers in Poland vs. Other Countries

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BKBeata KulikowskaBPBarbara PanasiukTMTakayasu Mori

Key Points

  • To assess the frequency of founder mutations in the BRCA1 and BRCA2 genes associated with hereditary breast cancer in Poland compared to other countries.
  • Conducted a literature review on BRCA1 and BRCA2 mutations
  • Compared hereditary breast cancer data from Poland and other countries
  • Evaluated the significance of genetic counseling in breast cancer treatment
  • Identified prevalent founder mutations in BRCA1 and BRCA2 genes in Poland
  • Reported differences in mutation frequency compared to other countries
  • Highlighted the importance of genetic counseling in managing hereditary breast cancer

Abstract

Breast cancer (BC) remains one of the most prevalent malignancies worldwide, and genetic factors may influence its development. Approximately 10–15% of all BCs are hereditary and known as Hereditary Breast Cancer (HBC). A remarkable family history and young onset are the strongest risk factors of HBC. The rapid development of genetic testing techniques has increased the detection rate of pathogenic and likely pathogenic variants in several genes associated with high, moderate, or low risk of HBC. This allowed us to identify the whole family at risk of HBC. Among hereditary cases, pathogenic variants (PVs) in the BRCA1 and BRCA2 genes are particularly notable, especially in certain populations where founder mutations (specific genetic variants originating from a common ancestor) are more prevalent. In this article, an overview of the current state of knowledge on HBC is provided, focusing on the frequency of founder mutations in the BRCA1 and BRCA2 genes in HBC in Poland compared to other countries. We will also highlight the role of genetic counseling in the diagnosis and treatment of BC, emphasizing its crucial importance in identifying genetic predispositions, selecting appropriate therapeutic strategies, and supporting patients and their families in making informed medical decisions.

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Cite This Study

Kulikowska et al. (2026) studied this question.

synapsesocial.com/papers/698433c8f1d9ada3c1fb135ehttps://doi.org/10.3390/cancers18030492
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

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  4. 4Founder mutations in early-onset, familial and bilateral breast cancer patients from Russia2007 · 78 citations
  5. 5The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%1996 · 385 citations