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本文引用的文献

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Epigenetic changes in histone acetylation underpin resistance to the topoisomerase I inhibitor irinotecan.组蛋白乙酰化的表观遗传变化是对拓扑异构酶I抑制剂伊立替康产生抗性的基础。
Nucleic Acids Res. 2017 Feb 17;45(3):1159-1176. doi: 10.1093/nar/gkw1026.
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Epidemiology of colorectal cancer.结直肠癌的流行病学
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The role of extracellular vesicles in mediating progression, metastasis and potential treatment of hepatocellular carcinoma.细胞外囊泡在介导肝细胞癌进展、转移及潜在治疗中的作用
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Molecular Diagnostics for Precision Medicine in Colorectal Cancer: Current Status and Future Perspective.结直肠癌精准医学中的分子诊断:现状与未来展望
Biomed Res Int. 2016;2016:9850690. doi: 10.1155/2016/9850690. Epub 2016 Sep 6.
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Outcomes after repeat hepatic resection for recurrent metastatic colorectal cancer: A population-based study.复发性转移性结直肠癌再次肝切除术后的结局:一项基于人群的研究。
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Response rates of hepatic arterial infusion pump therapy in patients with metastatic colorectal cancer liver metastases refractory to all standard chemotherapies.肝动脉灌注泵疗法对所有标准化疗均耐药的转移性结直肠癌肝转移患者的缓解率。
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Topoisomerase I expression is associated with prognosis in postoperative non-small cell lung cancer patients.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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8
Irinotecan chemotherapy combined with fluoropyrimidines versus irinotecan alone for overall survival and progression-free survival in patients with advanced and/or metastatic colorectal cancer.伊立替康化疗联合氟嘧啶与单纯伊立替康用于晚期和/或转移性结直肠癌患者的总生存期和无进展生存期的比较
Cochrane Database Syst Rev. 2016 Feb 12;2(2):CD008593. doi: 10.1002/14651858.CD008593.pub3.
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Cancer statistics, 2016.癌症统计数据,2016 年。
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10
Irinotecan, a key chemotherapeutic drug for metastatic colorectal cancer.伊立替康,一种用于转移性结直肠癌的关键化疗药物。
World J Gastroenterol. 2015 Nov 21;21(43):12234-48. doi: 10.3748/wjg.v21.i43.12234.

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.

DOI:10.1080/15384047.2017.1414754
PMID:29261002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5790385/
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。