PECEM (MD/PhD), Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Cátedras CONACYT- Instituto Nacional de Salud Pública, 62100, Cuernavaca, Morelos, Mexico.
Cell Mol Neurobiol. 2021 Aug;41(6):1285-1297. doi: 10.1007/s10571-020-00901-7. Epub 2020 Jun 13.
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.
星形细胞瘤是最常见的原发性脑肿瘤。星形细胞瘤的危险因素尚未完全明确;然而,种系遗传变异可导致 25%的胶质瘤发病风险。在这项研究中,我们评估了 AGT、已知在血管生成中起作用的 TP53、一种著名的肿瘤抑制基因和 DNA 修复基因 MGMT 中的变异与星形细胞瘤之间的关联,该研究在墨西哥人群中进行。我们进行了一项病例对照研究,纳入了 49 名患有 II-IV 级星形细胞瘤的成年墨西哥患者。在 Ion Torrent 平台上对 AGT、MGMT 和 TP53 的外显子和非翻译区进行了测序。使用 1000 基因组计划中的墨西哥裔个体作为对照。然后,在癌症基因组图谱泛种族星形细胞瘤验证队列中评估了我们队列中发现的变异。位于 AGT 的 rs1926723 变异(OR 2.74,1.40-5.36 95%CI)、MGMT 中的 rs7896488 变异(OR 3.43,1.17-10.10 95%CI)和 TP53 中的 rs4968187 变异(OR 2.48,1.26-4.88 95%CI)在经过多重检验校正后与星形细胞瘤风险显著相关。这是首次发现 AGT rs1926723 变异、TP53 rs4968187 变异和 MGMT rs7896488 变异与星形细胞瘤发病风险相关的研究。