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肿瘤拓扑异构酶 I 表达作为结直肠癌患者 CPT-11 化疗敏感性的生物学标志物。

Topoisomerase I expression in tumors as a biological marker for CPT-11 chemosensitivity in patients with colorectal cancer.

机构信息

Department of Surgery, Division of Surgical Oncology, School of Medicine, Tottori University, 36-1 Nishi-cho, Yonago, 683-8504, Japan.

出版信息

Surg Today. 2011 Sep;41(9):1196-9. doi: 10.1007/s00595-011-4546-7. Epub 2011 Aug 26.

DOI:10.1007/s00595-011-4546-7
PMID:21874414
Abstract

Irinotecan (CPT-11) is used as a first- and second-line chemotherapy for advanced or recurrent colorectal cancer (CRC). However, only 20%-30% of patients show an objective response to CPT-11 and the drug has severe toxicities, such as delayed-onset diarrhea, neutropenia, nausea, and vomiting. It is important to select patients who will demonstrate sensitivity to CPT-11 treatment to avoid unnecessary drug toxicities and to introduce anticancer treatment benefits to CRC patients. DNA topoisomerase I (Topo I) is essential for vital cellular processes such as DNA replication, transcription, translation, recombination, and repair. This article reviews the possibility of assessing Topo I protein expression in tumors as a biological marker for CPT-11 treatment in CRC.

摘要

伊立替康(CPT-11)是一种用于治疗晚期或复发性结直肠癌(CRC)的一线和二线化疗药物。然而,只有 20%-30%的患者对 CPT-11 有客观反应,且该药物具有严重的毒性,如迟发性腹泻、中性粒细胞减少、恶心和呕吐。选择对 CPT-11 治疗敏感的患者非常重要,以避免不必要的药物毒性,并为 CRC 患者带来抗癌治疗的益处。DNA 拓扑异构酶 I(Topo I)对于 DNA 复制、转录、翻译、重组和修复等重要的细胞过程至关重要。本文综述了评估肿瘤中 Topo I 蛋白表达作为 CRC 中 CPT-11 治疗的生物学标志物的可能性。

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Aprataxin tumor levels predict response of colorectal cancer patients to irinotecan-based treatment.Aprataxin 肿瘤水平可预测结直肠癌患者对伊立替康为基础治疗的反应。
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