ANO1 的表达与肺鳞癌中男性的生存率有关

Oluwadamilare I. Afolabi
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摘要

肺癌是癌症死亡的主要原因,其中肺鳞状细胞癌(LUSC)占很大比例。受分期、年龄和性别等临床病理因素的影响,肺鳞状细胞癌患者的预后差异很大,男性发病率较高,预后较女性差。因此,LUSC 预后建模和定制化治疗方法需要确定不同性别肿瘤和患者预后差异的生物机制。本研究利用《癌症基因组图谱》(TCGA)中的数据,描述了区分男性和女性乳腺癌的基因表达模式。具体来说,差异表达、生存和Cox回归分析评估了LUSC中ANO1(Anoctamin 1)表达和甲基化的预后价值。分析发现,与正常肺部和女性LUSC肿瘤中低得多的ANO1表达量相比,男性LUSC肿瘤亚群中的ANO1表达量明显过高。ANO1的高表达与男性患者的不良生存结果有关。ANO1基因体的高甲基化反映了基因表达,同样与生存率低有关。在多变量Cox回归分析中,ANO1的预后价值仍然显著,从而使其成为一个独立的预后生物标志物。ANO1在表达和预后价值上的明显性别差异表明了它在LUSC生存性别差异中的作用,突出了它作为生物标志物和性别特异性定制疗法靶点的潜力。
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ANO1 expression is associated with male survival in lung squamous cell carcinoma
Lung cancer is the leading cause of cancer deaths, with lung squamous cell carcinoma (LUSC) accounting for a substantial proportion of cases. LUSC exhibits significant variability in patient outcomes, influenced by clinicopathological factors such as stage, age, and sex, with men exhibiting higher rates of incidence and poorer outcomes compared to women. Therefore, prognosis modeling and customized approaches to LUSC therapy require the characterization of the biological mechanisms that differentiate tumors and patient outcomes across sexes. Using data from The Cancer Genome Atlas (TCGA), this study characterized gene expression patterns that distinguish male and female LUSC. Specifically, differential expression, survival, and Cox regression analyses assessed the prognostic value of ANO1 (Anoctamin 1) expression and methylation in LUSC. Analyses uncovered a significant overexpression of ANO1 in a subset of male LUSC tumors compared to a much lower expression in normal lung and female LUSC tumors. High ANO1 expression was associated with poor survival outcomes in male subjects. High ANO1 gene body methylation mirrored gene expression and was similarly associated with poor survival outcomes. ANO1’s prognostic value remained significant in a multivariate Cox regression analysis, establishing it as an independent prognostic biomarker. ANO1’s marked sex-specific differences in expression and prognostic value indicate its role in the sex disparity of LUSC survival, highlighting its potential as a biomarker and a target for sex-specific customized therapies.
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