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本文引用的文献

1
Phase II study of irinotecan and etoposide in patients with metastatic non-small-cell lung cancer.伊立替康与依托泊苷治疗转移性非小细胞肺癌患者的II期研究。
J Clin Oncol. 1997 Jan;15(1):304-9. doi: 10.1200/JCO.1997.15.1.304.
2
Treatment of patients with small-cell lung cancer refractory to etoposide and cisplatin with the topoisomerase I poison topotecan.用拓扑异构酶I抑制剂托泊替康治疗对依托泊苷和顺铂难治的小细胞肺癌患者。
J Clin Oncol. 1996 Oct;14(10):2785-90. doi: 10.1200/JCO.1996.14.10.2785.
3
Current perspectives on camptothecins in cancer treatment.喜树碱类药物在癌症治疗中的当前观点。
Br J Cancer. 1996 Aug;74(3):327-38. doi: 10.1038/bjc.1996.362.
4
DNA topoisomerase I and II in cancer chemotherapy: update and perspectives.癌症化疗中的DNA拓扑异构酶I和II：最新进展与展望
Cancer Chemother Pharmacol. 1993;32(2):103-8. doi: 10.1007/BF00685611.
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Phase I study of CPT-11 and etoposide in patients with refractory solid tumors.
J Clin Oncol. 1993 Oct;11(10):2030-5. doi: 10.1200/JCO.1993.11.10.2030.
6
Phase I and pharmacologic study of irinotecan and etoposide with recombinant human granulocyte colony-stimulating factor support for advanced lung cancer.伊立替康和依托泊苷联合重组人粒细胞集落刺激因子用于晚期肺癌的I期和药理学研究
J Clin Oncol. 1994 Sep;12(9):1833-41. doi: 10.1200/JCO.1994.12.9.1833.
7
Adriamycin-induced DNA damage mediated by mammalian DNA topoisomerase II.阿霉素诱导的由哺乳动物DNA拓扑异构酶II介导的DNA损伤。
Science. 1984 Oct 26;226(4673):466-8. doi: 10.1126/science.6093249.
8
Intercalative antitumor drugs interfere with the breakage-reunion reaction of mammalian DNA topoisomerase II.嵌入型抗肿瘤药物会干扰哺乳动物DNA拓扑异构酶II的断裂-重连反应。
J Biol Chem. 1984 Jul 25;259(14):9182-7.
9
Phase II study of camptothecin (NSC-100880) in the treatment of advanced gastrointestinal cancer.喜树碱（NSC - 100880）治疗晚期胃肠道癌的II期研究
Cancer Chemother Rep. 1972 Feb;56(1):95-101.
10
Treatment of malignant melanoma with camptothecin (NSC-100880).喜树碱（NSC-100880）治疗恶性黑色素瘤
Cancer Chemother Rep. 1972 Feb;56(1):103-5.

Combined inhibition of topoisomerases I and II--is this a worthwhile/feasible strategy?

作者信息

Vasey P A, Kaye S B

出版信息

Br J Cancer. 1997;76(11):1395-7. doi: 10.1038/bjc.1997.568.

DOI:10.1038/bjc.1997.568
PMID:9400932
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2228166/
Abstract
摘要