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拓扑异构酶 I 表达与术后非小细胞肺癌患者的预后相关。

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

机构信息

Division of Medical Oncology Beijing Chest Hospital, Capital Medical University Beijing China.

Division of Pathology Beijing Chest Hospital, Capital Medical University Beijing China.

出版信息

Thorac Cancer. 2016 Jul;7(4):486-94. doi: 10.1111/1759-7714.12359. Epub 2016 May 11.

Abstract

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.

摘要

背景

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。

方法

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。

结果

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)。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d54c/4930970/3c6328caad04/TCA-7-486-g002.jpg

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