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拓扑异构酶 1 和羧酸酯酶 2 的表达与转移性结直肠癌对伊立替康治疗的反应相关。

Expression of Topoisomerase 1 and carboxylesterase 2 correlates with irinotecan treatment response in metastatic colorectal cancer.

机构信息

a Department of Medical Oncology , The Fourth Affiliated Hospital of Guangxi Medical University , Liuzhou , Guangxi , China.

出版信息

Cancer Biol Ther. 2018 Mar 4;19(3):153-159. doi: 10.1080/15384047.2017.1414754. Epub 2018 Jan 16.

Abstract

Topoisomerase 1 (TOPO-1) and carboxylesterase 2 (CES-2) are found to play crucial roles in the pathogenesis of various cancers. The prognostic role of TOPO-1 and CES-2 in patients with metastatic colorectal cancer (mCRC) who underwent irinotecan chemotherapy was largely unknown. In the current study, we assessed the expression of TOPO-1 and CES-2 in mCRC and analyzed its potential relevance to irinotecan based therapy. A total of 98 patients with mCRC were included in this study. The expression of TOPO-1 and CES-2 in mCRC tissues was evaluated by immunohistochemistry. For TOPO-1, 46 patients showed high expression and 52 patients showed low expression. For CES-2, 53 patients showed high expression and 45 patients showed low expression. The correlation between TOPO-1 or CES-2 expression and clinicopathological characteristics of mCRC patients was analyzed. Neither TOPO-1 nor CES-2 had significant correlation with age, gender, tumor site, tumor grade and metastatic sites in mCRC patients. However, high expression of CES-2 but not TOP-1 was positively correlated with better curative effect. Kaplan-Meier and log-rank test were applied to assess the correlation between progression-free survival (PFS)/overall survival (OS) and TOPO-1 or CES-2 expression in mCRC patients. High expression of TOPO-1 and CES-2 are correlated with longer PFS and OS. In summary, our findings suggest that TOPO-1 and CES-2 may play important roles irinotecan sensitivity in mCRC patients. Evaluation of expression of TOPO-1 and CES-2 may provide preliminary clinical evidence for the management of irinotecan-based therapy in mCRC patients.

摘要

拓扑异构酶 1(TOPO-1)和羧酸酯酶 2(CES-2)被发现在各种癌症的发病机制中起着关键作用。TOPO-1 和 CES-2 在接受伊立替康化疗的转移性结直肠癌(mCRC)患者中的预后作用在很大程度上尚不清楚。在本研究中,我们评估了 mCRC 中 TOPO-1 和 CES-2 的表达,并分析了其与伊立替康为基础的治疗的潜在相关性。本研究共纳入 98 例 mCRC 患者。采用免疫组织化学法检测 mCRC 组织中 TOPO-1 和 CES-2 的表达。TOPO-1 中,46 例患者高表达,52 例患者低表达。CES-2 中,53 例患者高表达,45 例患者低表达。分析 TOPO-1 或 CES-2 表达与 mCRC 患者临床病理特征的相关性。TOPO-1 或 CES-2 的表达与 mCRC 患者的年龄、性别、肿瘤部位、肿瘤分级和转移部位均无显著相关性。然而,CES-2 的高表达而非 TOPO-1 的高表达与更好的疗效呈正相关。Kaplan-Meier 和对数秩检验用于评估 mCRC 患者无进展生存期(PFS)/总生存期(OS)与 TOPO-1 或 CES-2 表达之间的相关性。TOPO-1 和 CES-2 的高表达与更长的 PFS 和 OS 相关。总之,我们的研究结果表明,TOPO-1 和 CES-2 可能在 mCRC 患者对伊立替康的敏感性中发挥重要作用。TOPO-1 和 CES-2 的表达评估可能为 mCRC 患者伊立替康为基础的治疗管理提供初步的临床证据。

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