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Mutational Analysis of Oncogenic AKT1 Gene Associated with Breast Cancer Risk in the High Altitude Ecuadorian Mestizo Population

机译:高海拔厄瓜多尔混血儿人群致癌性AKT1基因突变与乳腺癌风险的突变分析

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摘要

Breast cancer is the leading cause of cancer-related death among women worldwide. AKT1 encodes the kinase B alpha protein. The rs121434592, rs12881616, rs11555432, rs11555431, rs2494732, and rs3803304 single nucleotide polymorphisms have been identified in the AKT1 kinase gene. Activated AKT1 phosphorylates downstream substrates regulating cell growth, metabolism, apoptosis, angiogenesis, and drug responses. It is essential to know how breast cancer risk is associated with histopathological and immunohistochemical characteristics and genotype polymorphisms in a high altitude Ecuadorian mestizo population. This is a retrospective case-control study. DNA was extracted from 185 healthy and 91 affected women who live 2,800 meters above sea level. Genotypes were determined by genomic sequencing. We found a possible association between the noncoding intronic variant rs3803304 and breast cancer risk development: GG (odds ratio [OR] = 5.2; 95% confidence interval [CI] = 1.3-20.9; P ≤ 0.05; Q > 0.05). Regarding pathologic characteristics, we found significant risk between estrogen receptor, progesterone receptor, and HER2 status and molecular subtypes (P ≤ 0.001; Q ≤ 0.05). On the other hand, we did not find risk between variants and histopathological characteristics. Despite the small sample size, we found that the intronic variant, AKT1 rs3803304, may act as a predictive biomarker in the risk of developing breast cancer in the high altitude Ecuadorian mestizo population.
机译:乳腺癌是全世界女性与癌症相关的死亡的主要原因。 AKT1编码激酶Bα蛋白。已在AKT1激酶基因中鉴定出rs121434592,rs12881616,rs11555432,rs11555431,rs2494732和rs3803304单核苷酸多态性。活化的AKT1磷酸化下游底物,调节细胞生长,代谢,凋亡,血管生成和药物反应。了解乳腺癌风险与高海拔厄瓜多尔混血儿群体的组织病理学和免疫组织化学特征以及基因型多态性之间的关系至关重要。这是一项回顾性病例对照研究。从海拔2800米的185名健康女性和91名受影响女性中提取DNA。通过基因组测序确定基因型。我们发现非编码内含子rs3803304与乳腺癌风险发展之间可能存在关联:GG(优势比[OR] = 5.2; 95%置信区间[CI] = 1.3-20.9; P≤0.05; Q> 0.05)。关于病理特征,我们发现雌激素受体,孕激素受体,HER2状态和分子亚型之间存在显着风险(P≤0.001; Q≤0.05)。另一方面,我们没有发现变异与组织病理学特征之间存在风险。尽管样本量很小,但我们发现内含子变体AKT1 rs3803304在高海拔的厄瓜多尔混血儿人群中可能作为罹患乳腺癌风险的预测性生物标志物。

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