| Literature DB >> 32535722 |
José Alberto Carlos-Escalante1, Liliana Gómez-Flores-Ramos2, Xiaopeng Bian3, Alexander Perdomo-Pantoja4, Kelvin César de Andrade5, Sonia Iliana Mejía-Pérez6,7, Bernardo Cacho-Díaz8, Rodrigo González-Barrios9, Nancy Reynoso-Noverón9, Ernesto Soto-Reyes10, Thalía Estefanía Sánchez-Correa7, Lissania Guerra-Calderas10, Chunhua Yan3, Qingrong Chen3, Clementina Castro-Hernández11, Silvia Vidal-Millán12, Lucía Taja-Chayeb9, Olga Gutiérrez9, Rosa María Álvarez-Gómez12, Juan Luis Gómez-Amador7, Patricia Ostrosky-Wegman13, Alejandro Mohar-Betancourt11, Luis Alonso Herrera-Montalvo11,14, Teresa Corona15, Daoud Meerzaman3, Talia Wegman-Ostrosky16.
Abstract
Astrocytoma is the most common type of primary brain tumor. The risk factors for astrocytoma are poorly understood; however, germline genetic variants account for 25% of the risk of developing gliomas. In this study, we assessed the risk of astrocytoma associated with variants in AGT, known by its role in angiogenesis, TP53, a well-known tumor suppressor and the DNA repair gene MGMT in a Mexican population. A case-control study was performed in 49 adult Mexican patients with grade II-IV astrocytoma. Sequencing of exons and untranslated regions of AGT, MGMT, and TP53 from was carried in an Ion Torrent platform. Individuals with Mexican Ancestry from the 1000 Genomes Project were used as controls. Variants found in our cohort were then assessed in a The Cancer Genome Atlas astrocytoma pan-ethnic validation cohort. Variants rs1926723 located in AGT (OR 2.74, 1.40-5.36 95% CI), rs7896488 in MGMT (OR 3.43, 1.17-10.10 95% CI), and rs4968187 in TP53 (OR 2.48, 1.26-4.88 95% CI) were significantly associated with the risk of astrocytoma after multiple-testing correction. This is the first study where the AGT rs1926723 variant, TP53 rs4968187, and MGMT rs7896488 were found to be associated with the risk of developing an astrocytoma.Entities:
Keywords: Astrocytoma; Germline genetic variant; Mexican population; Risk
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Year: 2020 PMID: 32535722 DOI: 10.1007/s10571-020-00901-7
Source DB: PubMed Journal: Cell Mol Neurobiol ISSN: 0272-4340 Impact factor: 5.046