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DNA methylation of leukocytes from sporadic breast cancer patients and healthy controls in Latin American population

ABSTRACT: DNA methylation of leukocytes from sporadic breast cancer patients and healthy controls in Latin American population

PROVIDER: PRJNA625303 | ENA |

REPOSITORIES: ENA

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DNA methylation of leukocytes from sporadic breast cancer patients and healthy controls in Latin American population

Project description:The study aimed to compare the DNA methylation differences between blood samples from sporadic breast cancer patients and healthy controls from a well-defined cohort in Uruguayan population. Infinium methylation arrays (450K Illumina) are used to identify genome-wide methylation differences between groups. The identified differently methylated CpG were further analyzed in an independent cohort of 80 breast cancer patients and 80 healthy controls.

2021-02-08 | GSE148663 | GEO

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Genomic Diversity in Sporadic Breast Cancer in a Latin American Population.

Project description:Among Latin American women, breast cancer incidences vary across populations. Uruguay and Argentina have the highest rates in South America, which are mainly attributed to strong, genetic European contributions. Most genetic variants associated with breast cancer were described in European populations. However, the vast majority of genetic contributors to breast cancer risk remain unknown. Here, we report the results of a candidate gene association study of sporadic breast cancer in 176 cases and 183 controls in the Uruguayan population. We analyzed 141 variants from 98 loci that have been associated with overall breast cancer risk in European populations. We found weak evidence for the association of risk variants rs294174 (ESR1), rs16886165 (MAP3K1), rs2214681 (CNTNAP2), rs4237855 (VDR), rs9594579 (RANKL), rs8183919 (PTGIS), rs2981582 (FGFR2), and rs1799950 (BRCA1) with sporadic breast cancer. These results provide useful insight into the genetic susceptibility to sporadic breast cancer in the Uruguayan population and support the use of genetic risk scores for individualized screening and prevention.

| S-EPMC7716199 | biostudies-literature

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