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Landscape of Germline Genetic Variants in AGT, MGMT, and TP53 in Mexican Adult Patients with Astrocytoma.

José Alberto Carlos-EscalanteLiliana Gómez Flores-RamosXiaopeng BianAlexander Perdomo-PantojaKelvin César de AndradeSonia Iliana Mejía-PérezBernardo Cacho-DíazRodrigo González-BarriosNancy Reynoso NoverónErnesto Soto-ReyesThalía Estefanía Sánchez-CorreaLissania Guerra-CalderasChunhua YanQingrong ChenClementina Castro-HernándezSilvia Vidal-MillánLucía Taja-ChayebOlga GutiérrezRosa Maria ÁlvarezJuan Luis Gómez-AmadorPatricia Ostrosky-WegmanAlejandro Mohar BetancourtLuis Alonso Herrera-MontalvoTeresa CoronaDaoud MeerzamanTalia Wegman-Ostrosky
Published in: Cellular and molecular neurobiology (2020)
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.
Keyphrases
  • dna repair
  • copy number
  • dna damage
  • single cell
  • genome wide
  • endothelial cells
  • high grade
  • dna methylation
  • quality improvement
  • gene expression
  • young adults
  • squamous cell