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Topoisomerase II|[alpha]| mRNA and protein expression in ovarian carcinoma: correlation with clinicopathological factors and prognosis

机译:拓扑异构酶II |α|卵巢癌中mRNA和蛋白表达与临床病理因素及预后的关系

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Topoisomerase IIα (Top IIα) is a nuclear enzyme that plays a central role in DNA metabolism, and is a molecular target for a variety of chemotherapeutic agents. Top IIα has recently gained attention as a biomarker for therapy response and patient survival. In this study, we attempted to assess the feasibility of measuring Top IIα gene expression in RNA, isolated from archival formalin-fixed paraffin-embedded tissue specimens, which are used routinely in pathology laboratories. We have employed a new technique on the basis of magnetic particles’ separation and purification of nucleic acids, and evaluated both protein and mRNA expressions from the same routinely processed tissue blocks. We investigated the expression of Top IIα mRNA and protein by real-time reverse transcription polymerase chain reaction and immunohistochemistry, in a cohort of 133 primary ovarian carcinomas, and evaluated the association between Top IIα expression and clincopathological variables as well as patient outcome. Elevated Top IIα mRNA expression was observed in high-grade tumors (P=0.003) and advanced stage disease (P=0.011). In univariate Kaplan–Meier analysis, patients with higher expression of Top IIα nuclear protein had a significantly decreased overall survival (P=0.045). Interestingly, we detected cytoplasmic protein expression of Top IIα in a subset of samples. Cytoplasmic expression of Top IIα was associated with the expression of chromosomal region maintenance/exportin 1 (CRM1)—a nuclear export protein (P=0.008). Our study suggests that Top IIα overexpression is involved in the progression of ovarian cancer in a subset of the patients. Our results encourage the further evaluation of the prognostic and predictive values of Top IIα expression in ovarian carcinoma, which might help to assess the patients’ risk profile, and the planning of an individualized therapy.
机译:拓扑异构酶IIα(TopIIα)是一种核酶,在DNA代谢中起着核心作用,并且是多种化学治疗剂的分子靶标。最近,TopIIα作为治疗反应和患者生存的生物标志物已引起关注。在这项研究中,我们尝试评估测量RNA中TopIIα基因表达的可行性,该基因是从档案福尔马林固定的石蜡包埋的组织标本中分离的,这些标本通常在病理实验室中使用。我们基于磁性粒子的分离和核酸纯化采用了一项新技术,并评估了来自相同常规处理组织块的蛋白质和mRNA表达。我们通过实时逆转录聚合酶链反应和免疫组织化学,在133个原发性卵巢癌队列中研究了TopIIαmRNA和蛋白的表达,并评估了TopIIα表达与临床病理变量以及患者预后之间的关联。在高级肿瘤(P = 0.003)和晚期疾病(P = 0.011)中观察到TopIIαmRNA表达升高。在单变量Kaplan–Meier分析中,TopIIα核蛋白高表达患者的总生存期显着降低(P = 0.045)。有趣的是,我们在一部分样本中检测到了TopIIα的胞质蛋白表达。 TopIIα的胞质表达与染色体区域维持/输出蛋白1(CRM1)的表达有关-一种核输出蛋白(P = 0.008)。我们的研究表明,TopIIα过表达与部分患者的卵巢癌进展有关。我们的结果鼓励进一步评估卵巢癌中TopIIα表达的预后和预测价值,这可能有助于评估患者的风险状况,并制定个性化治疗方案。

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