低5-羟甲基胞嘧啶水平是局部晚期乳腺癌高组织学分级的独立预测因子

D. Prada, J. Díaz-Chávez, O. Peña-Curiel, Marissa Vargas Ramírez, E. Colicino, C. Villarreal-Garza, P. Cabrera-Galeana, T. Castro-Belio, N. Reynoso, M. Andonegui, G. Navarro, León Dcd, Y. Villaseñor, A. López-Saavedra, C. Arriaga-Canon, Cortés Cc, C. Caro, G. Am, E. Bargalló, Herrera La
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(standard deviation [SD]: 9,54 yrs.), tumors showed a mean diameter of 6.53 cm (SD: 3.06 cm) at diagnosis, most of the patients showed overweight or obesity (77.3%) and most of them were locally advanced stage (n=111). A statistically significant and negative correlation between 5hmC levels and age in ER/PR-negative tumors (β = -0.028, 95% confidence interval [95%CI]: -0.045, -0.010, p-value = 0.005) and in triple negative tumors (β = -0.023, 95%CI: -0.044, -0.001, p-value = 0.046) was observed using mixed effects linear models. We also observed a negative correlation between 5hmC levels and an increased levels of cell proliferation markers, including Ki67 (r = -0.16, p-value < 0.01) and minichromosome maintenance complex component 2 [MCM2] (r = -0.21, p-value = 0.03). 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引用次数: 0

摘要

背景:乳腺癌是世界范围内癌症死亡的主要原因。在墨西哥,大多数病例在当地被诊断为晚期,这与预后不良有关。最近的研究表明,5-羟甲基胞嘧啶(5hmC)水平可能是癌症预后的一个标志。然而,5hmC作为乳腺癌组织病理学改变的预测因子的作用尚未得到充分研究。结果:我们评估了来自乳腺癌患者的样本(N=141),平均年龄为50.12岁。(标准差[SD]: 9.54岁),诊断时肿瘤平均直径为6.53 cm (SD: 3.06 cm),多数患者表现为超重或肥胖(77.3%),多数为局部晚期(n=111)。在ER/ pr阴性肿瘤(β = -0.028, 95%可信区间[95% ci]: -0.045, -0.010, p值= 0.005)和三阴性肿瘤(β = -0.023, 95% ci: -0.044, -0.001, p值= 0.046)中,使用混合效应线性模型观察到5hmC水平与年龄呈统计学显著负相关(β = -0.028, 95%可信区间[95% ci]: -0.010, p值= 0.005)。我们还观察到5hmC水平与细胞增殖标志物Ki67 (r = -0.16, p值< 0.01)和微小染色体维持复合物组分2 [MCM2] (r = -0.21, p值= 0.03)水平升高呈负相关。最后,使用混合效应模型,我们确定5hmC水平是局部晚期乳腺癌患者晚期组织学分级的独立预测因子(β = -0.077, 95%CI -0.142, -0.011, p = 0.022)。我们没有观察到5hmC水平与完全病理反应或无复发生存相关的差异。结论:本研究提示低5hmC可能作为局部晚期乳腺癌患者不良组织病理学特征的潜在标志物,突出了其作为一种有用的临床生物标志物的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low 5-hydroxymethylcytosine level is an independent predictor of high histological grade in locally advanced breast cancer
Background: Breast cancer is a major cause of cancer mortality worldwide. In Mexico, most cases are diagnosed in locally advanced stages, which is associated with a poor prognosis. Recent studies have suggested that 5-hydroxymethylcytosine (5hmC) levels could be a prognostic marker in cancer. However, the role of 5hmC as a predictor of histopathological alterations in breast cancer have not been fully studied. Results: We evaluated samples from patients with breast cancer (N=141), with a mean age of 50.12 yrs. (standard deviation [SD]: 9,54 yrs.), tumors showed a mean diameter of 6.53 cm (SD: 3.06 cm) at diagnosis, most of the patients showed overweight or obesity (77.3%) and most of them were locally advanced stage (n=111). A statistically significant and negative correlation between 5hmC levels and age in ER/PR-negative tumors (β = -0.028, 95% confidence interval [95%CI]: -0.045, -0.010, p-value = 0.005) and in triple negative tumors (β = -0.023, 95%CI: -0.044, -0.001, p-value = 0.046) was observed using mixed effects linear models. We also observed a negative correlation between 5hmC levels and an increased levels of cell proliferation markers, including Ki67 (r = -0.16, p-value < 0.01) and minichromosome maintenance complex component 2 [MCM2] (r = -0.21, p-value = 0.03). Finally, and using mixed effects models, we determined that the 5hmC level was an independent predictor of advanced histological grade in locally advanced breast cancer patients (β = -0.077, 95%CI -0.142, -0.011, p = 0.022). We did not observe differences associated with complete pathological response or free-relapse survival according to 5hmC level. Conclusions: This study suggests that low 5hmC may serve as potential marker of adverse histopathological characteristics in locally advanced breast cancer patients, highlighting its potential as a useful clinical biomarker.
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