Division of Medical Oncology Beijing Chest Hospital, Capital Medical University Beijing China.
Division of Pathology Beijing Chest Hospital, Capital Medical University Beijing China.
Thorac Cancer. 2016 Jul;7(4):486-94. doi: 10.1111/1759-7714.12359. Epub 2016 May 11.
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.
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.
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).
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.
生物标志物可能有助于改善非小细胞肺癌(NSCLC)的预后。然而,拓扑异构酶 I(Topo I)对 NSCLC 的预后影响尚不清楚。我们评估了术后 NSCLC 患者肿瘤 Topo I 和胸苷酸合成酶(TS)蛋白表达的临床病理和预后意义。
纳入 115 例术后 NSCLC 患者。采用免疫组织化学法检测切除肿瘤中的 Topo I 和 TS 蛋白。分析 Topo I/TS 蛋白表达与患者临床病理特征和结局的相关性。
发现 57 例(49.6%)肿瘤中 Topo I 表达增加。高表达和低表达 Topo I 患者的肿瘤最大直径有显著差异(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相关(P=0.037)。低表达 Topo I 的患者总生存期(OS)明显长于高表达者(P=0.004)。Topo I 表达与 OS 的相关性在鳞状细胞癌患者(P=0.030)和病理肿瘤淋巴结转移分期 I 患者(P=0.027)中得到证实。肿瘤组织中 Topo I 表达与 TS 表达呈正相关(R=0.251,P=0.007)。
低表达 Topo I 是术后 NSCLC 患者 OS 更长的独立预后因素,尤其在鳞状细胞癌患者中。切除肿瘤组织中 TS 和 Topo I 的表达存在相关性。