%0 Journal Article
%T A Molecular Characterization of the Allelic Expression of the BRCA1 Founder Δ9-12 Pathogenic Variant and Its Potential Clinical Relevance in Hereditary Cancer.
%A Dominguez-Ortiz J
%A Álvarez-Gómez RM
%A Montiel-Manríquez R
%A Cedro-Tanda A
%A Alcaraz N
%A Castro-Hernández C
%A Bautista-Hinojosa L
%A Contreras-Espinosa L
%A Torres-Maldonado L
%A Fragoso-Ontiveros V
%A Sánchez-Contreras Y
%A González-Barrios R
%A Fuente-Hernández MA
%A Mejía-Aguayo ML
%A Juárez-Figueroa U
%A Padua-Bracho A
%A Sosa-León R
%A Obregon-Serrano G
%A Vidal-Millán S
%A Núñez-Martínez PM
%A Pedroza-Torres A
%A Nicasio-Arzeta S
%A Rodríguez A
%A Luna F
%A Cisneros-Soberanis F
%A Frías S
%A Arriaga-Canon C
%A Herrera-Montalvo LA
%J Int J Mol Sci
%V 25
%N 12
%D 2024 Jun 20
%M 38928478
%F 6.208
%R 10.3390/ijms25126773
%X Hereditary breast and ovarian cancer (HBOC) syndrome is a genetic condition that increases the risk of breast cancer by 80% and that of ovarian cancer by 40%. The most common pathogenic variants (PVs) causing HBOC occur in the BRCA1 gene, with more than 3850 reported mutations in the gene sequence. The prevalence of specific PVs in BRCA1 has increased across populations due to the effect of founder mutations. Therefore, when a founder mutation is identified, it becomes key to improving cancer risk characterization and effective screening protocols. The only founder mutation described in the Mexican population is the deletion of exons 9 to 12 of BRCA1 (BRCA1Δ9-12), and its description focuses on the gene sequence, but no transcription profiles have been generated for individuals who carry this gene. In this study, we describe the transcription profiles of cancer patients and healthy individuals who were heterozygous for PV BRCA1Δ9-12 by analyzing the differential expression of both alleles compared with the homozygous BRCA1 control group using RT-qPCR, and we describe the isoforms produced by the BRCA1 wild-type and BRCA1Δ9-12 alleles using nanopore long-sequencing. Using the Kruskal-Wallis test, our results showed a similar transcript expression of the wild-type allele between the healthy heterozygous group and the homozygous BRCA1 control group. An association between the recurrence and increased expression of both alleles in HBOC patients was also observed. An analysis of the sequences indicated four wild-type isoforms with diagnostic potential for discerning individuals who carry the PV BRCA1Δ9-12 and identifying which of them has developed cancer.