首页> 美国卫生研究院文献>International Journal of Clinical and Experimental Pathology >Low nuclear zinc finger and BTB domain containing 7A expression is an independent prognostic factor for recurrence-free survival in invasive ductal carcinoma of the breast
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Low nuclear zinc finger and BTB domain containing 7A expression is an independent prognostic factor for recurrence-free survival in invasive ductal carcinoma of the breast

机译:低核锌指和包含7A表达的BTB结构域是乳腺浸润性导管癌无复发生存的独立预后因素

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摘要

The role of zinc finger and BTB domain containing 7A (ZBTB7A) in oncogenesis has been shown to be context-dependent, participating in pro-oncogenic or oncosuppressive mechanisms by directly regulating gene transcription or by interacting with other regulatory proteins. Alterations in ZBTB7A expression have been associated with worse prognosis. We examined ZBTB7A protein expression in breast carcinoma tissue samples and analyzed its clinical and prognostic significance. Tissue microarray blocks from 196 cases of invasive ductal carcinoma (IDC) were immunostained and <65% positively stained tumor cell nuclei were defined as low ZBTB7A expression. Of 196 IDC cases, 120 (61.2%) showed low ZBTB7A expression. Low nuclear ZBTB7A expression was associated with larger tumor size, higher histological grade, estrogen receptor negativity, progesterone receptor negativity, triple negativity, and recurrence. Cytoplasmic ZBTB7A expression was not associated with any clinicopathological characteristics. In univariate survival analysis, nuclear ZBTB7A expression did not affect overall or recurrence-free survival. However, multivariate survival analysis revealed that ZBTB7A independently predicted recurrence-free survival of IDC patients. Reduced ZBTB7A expression is associated with aggressive oncogenic behavior of IDC. ZBTB7A expression may be a novel prognostic biomarker for predicting recurrence-free survival of IDC patients.
机译:锌指和含有7A的BTB结构域(ZBTB7A)在肿瘤发生中的作用已显示是上下文相关的,通过直接调节基因转录或与其他调节蛋白相互作用,参与促癌或抑癌机制。 ZBTB7A表达的改变与预后不良有关。我们检查了乳腺癌组织样品中ZBTB7A蛋白的表达,并分析了其临床和预后意义。对来自196例浸润性导管癌(IDC)的组织微阵列芯片进行了免疫染色,并且将<65%的阳性染色肿瘤细胞核定义为ZBTB7A低表达。在196例IDC病例中,有120例(61.2%)显示ZBTB7A低表达。 ZBTB7A低核表达与更大的肿瘤大小,更高的组织学等级,雌激素受体阴性,孕激素受体阴性,三阴性和复发有关。细胞质ZBTB7A表达与任何临床病理特征无关。在单变量生存分析中,核ZBTB7A表达不影响总体生存或无复发生存。但是,多变量生存分析显示ZBTB7A独立预测IDC患者的无复发生存。 ZBTB7A表达降低与IDC的侵袭性致癌行为有关。 ZBTB7A表达可能是预测IDC患者无复发生存的新型预后生物标志物。

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