BRCA1/BRCA2 Mutations Shaped by Ancient Consanguinity Practice in Southern Mediterranean Populations
Autor: | Belaiba, Fadoua, Medimegh, Imene, Bidet, Yannick, Boussetta, Sami, Baroudi, Olfa, Mezlini, Amel, Bignon, Yves Jean, Benammar El gaaied, Amel |
---|---|
Přispěvatelé: | Imagerie Moléculaire et Stratégies Théranostiques (IMoST), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Clermont Auvergne [2017-2020] (UCA [2017-2020]), The Lymphoma Academic Research Organisation [Lyon] (LYSARC), Departement Medecine Oncologique [Tunis], Institut Salah Azaiz [Tunis] (ISA) |
Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
BRCA2 Protein
recurrence Base Sequence BRCA1 Protein Incidence BRCA2/1Mutation analysis Breast Neoplasms [SDV.CAN]Life Sciences [q-bio]/Cancer Middle Aged Breast cancer consanguinity Case-Control Studies Humans Family Female Amino Acid Sequence Neoplasm Recurrence Local penetrance Frameshift Mutation skin and connective tissue diseases Research Article |
Zdroj: | Asian Pacific Journal of Cancer Prevention Asian Pacific Journal of Cancer Prevention, Asian Pacific Education Press Ltd., 2018, pp.2963-2972. ⟨10.22034/APJCP.2018.19.10.2963⟩ Asian Pacific Journal of Cancer Prevention : APJCP |
ISSN: | 1513-7368 |
DOI: | 10.22034/APJCP.2018.19.10.2963⟩ |
Popis: | International audience; The aim of this study is to investigate the involvement of consanguinity on BRCA1/2 mutation incidence in Southern Mediterranean populations and to confirm their low penetrance by comparison of their recurrence in sporadic and familial breast cancer in a context of ancient consanguinity practice. Our study comprises of two parts: First, a comparison of the consanguinity rates of the South Mediterranean countries in a relationship with the frequency of BRCA1 deleterious mutations in breast cancer families and the recurrence of these mutations. Second, we investigated 23patients with a family history of breast cancer, 51 patients without a family history of breast cancer using next-generation sequencing of BRCA2 and then confirmed by Sanger sequencing for the novel mutation. As results, we clearly show a strong relationship between the frequency of BRCA1 deleterious mutations in breast cancer families and rate of consanguinity, since they are significantly inversely correlated. Four deleterious mutations were found in BRCA2 gene including a novel frame-shift mutationc.9382_9383dup in a patient with familial breast cancer and three other frame-shift mutations c.6591_6592del, c.1310_1313del and c.7654dup in patients with sporadic breast cancer.These results are discussed in a context of selective pressure of ancient consanguinity practice. In conclusion, the study of BRCA1/2 gene in Southern Mediterranean countries revealed low penetrance recurrent mutations in sporadic and familial breast cancer. These mutations have been selected in a context of ancient consanguinity practice along with protective genetic and environmental factors. |
Databáze: | OpenAIRE |
Externí odkaz: |