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Topoisomerase I expression is associated with prognosis in postoperative non‐small cell lung cancer patients

机译:拓扑异构酶I表达与术后非小细胞肺癌患者的预后相关

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Background Biomarkers may help to improve non-small cell lung cancer (NSCLC) prognosis. However, the prognostic effect of topoisomerase I (Topo I) on NSCLC is unknown. We evaluated the clinicopathologic and prognostic significance of tumor Topo I and thymidylate synthase (TS) protein expression in postoperative NSCLC patients. Methods One hundred and fifteen patients with postoperative NSCLC were enrolled. Topo I and TS protein were detected in removed tumors by immunohistochemistry. The correlations between Topo I/TS protein expression and clinicopathologic characters and outcomes of patients were analyzed. Results Increased expression of Topo I was found in 57 (49.6%) tumors. The largest diameter of the tumor was significantly different between patients with high and low Topo I expression ( P = 0.035). TS staining showed that 35 (30.4%) carcinomas were TS positive. The level of TS expression was correlated with tumor differentiation ( P = 0.037). Patients with low Topo I expression had significantly longer overall survival (OS) than those with high expression ( P = 0.004). The correlation between Topo I expression and OS was demonstrated among patients with squamous cell carcinoma ( P = 0.030) and patients in pathological tumor node metastasis stage I ( P = 0.027). Topo I expression was positively correlated with TS expression in tumor tissue (R = 0.251, P = 0.007). Conclusions Low Topo I expression is an independent favorable prognostic factor for longer OS in postoperative NSCLC patients, especially in squamous cell carcinoma. There is a correlation between the expression of TS and Topo I in removed tumor tissue.
机译:背景生物标志物可能有助于改善非小细胞肺癌(NSCLC)的预后。但是,拓扑异构酶I(Topo I)对NSCLC的预后作用尚不清楚。我们评估了术后NSCLC患者肿瘤Topo I和胸苷酸合酶(TS)蛋白表达的临床病理和预后意义。方法纳入115例术后NSCLC患者。通过免疫组织化学在切除的肿瘤中检测到Topo I和TS蛋白。分析了Topo I / TS蛋白表达与临床病理特征和患者预后之间的相关性。结果在57例(49.6%)肿瘤中发现了Topo I的表达增加。 Topo I高表达和低表达的患者的最大肿瘤直径显着不同(P = 0.035)。 TS染色显示35例(30.4%)癌为TS阳性。 TS表达水平与肿瘤分化程度相关(P = 0.037)。 Topo I表达低的患者的总生存期(OS)明显高于高表达的患者(P = 0.004)。在鳞状细胞癌患者(P = 0.030)和处于病理性肿瘤淋巴结转移I期的患者(P = 0.027)证明了Topo I表达与OS之间的相关性。肿瘤组织中Topo I的表达与TS表达呈正相关(R = 0.251,P = 0.007)。结论Topo I低表达是NSCLC术后尤其是鳞状细胞癌患者较长OS的独立预后因素。在切除的肿瘤组织中TS和Topo I的表达之间存在相关性。

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