aplotypes of single cancer driver genes and their local ancestry in a highly admixed long-lived population of Northeast Brazi

Autor(es)

Galdino Galisa, Steffany Larissa ^[1] ; Jacob, Priscila Lima ^[1] ; de Farias, Allysson Allan ^{[2, 1]} ; Lemes, Renan Barbosa ^[2] ; Alves, Leandro Ucela ^{[2, 1]} ; Leite Nobrega, Julia Cristina ^[1] ; Zatz, Mayana ^[2] ; Santos, Silvana ^{[1, 3]} ; Weller, Mathias ^{[1, 3]}

Afiliação do(s) autor(es)

^[1] Univ Estadual Paraiba UEPB, Programa Posgrad Saude Publ, Nucleo Estudos Genet & Educ, Rua Domitila Cabral de Castro S-N, 32 Ander, Campina Grande, Paraiba - Brazil

^[2] Univ Sao Paulo, Dept Genet & Biol Evolut, Sao Paulo, SP - Brazil

^[3] Univ Estadual Paraiba UEPB, Dept Biol, Campina Grande, Paraiba - Brazil

• Tipo de documento: Artigo Científico
• Fonte: GENETICS AND MOLECULAR BIOLOGY; v. 45, n. 1 2022.
• Citações Web of Science: 0

Resumo

Admixed populations have not been examined in detail in cancer genetic studies. Here, we inferred the local ancestry of cancer-associated single nucleotide polymorphisms (SNPs) and haplotypes of a highly admixed Brazilian population. SNP array was used to genotype 73 unrelated individuals aged 80-102 years. Local ancestry inference was performed by merging genotyped regions with phase three data from the 1000 Genomes Project Consortium using RFmix. The average ancestry tract length was 9.12-81.71 megabases. Strong linkage disequilibrium was detected in 48 haplotypes containing 35 SNPs in 10 cancer driver genes. All together, 19 risk and eight protective alleles were identified in 23 out of 48 haplotypes. Homozygous individuals were mainly of European ancestry, whereas heterozygotes had at least one Native American and one African ancestry tract. Native-American ancestry for homozygous individuals with risk alleles for HNF1B, CDH1, and BRCA1 was inferred for the first time. Results indicated that analysis of SNP polymorphism in the present admixed population has a high potential to identify new ancestry-associated alleles and haplotypes that modify cancer susceptibility differentially in distinct human populations. Future case-control studies with populations with a complex history of admixture could help elucidate ancestry-associated biological differences in cancer incidence and therapeutic outcomes. (AU)

• Processo FAPESP: 14/50931-3 - INCT 2014 - Envelhecimento e Doenças Genéticas: Genômica e Metagenômica
• Beneficiário: Mayana Zatz
• Modalidade de apoio: Auxílio à Pesquisa - Temático
• Processo FAPESP: 13/08028-1 - CEGH-CEL - Centro de Estudos do Genoma Humano e de Células-Tronco
• Beneficiário: Mayana Zatz
• Modalidade de apoio: Auxílio à Pesquisa - Centros de Pesquisa, Inovação e Difusão - CEPIDs