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      Preclinical evaluation of CPT-11 and its active metabolite SN-38.

      Seminars in Oncology
      Animals, Antineoplastic Agents, Phytogenic, pharmacology, Camptothecin, administration & dosage, analogs & derivatives, toxicity, DNA Damage, Drug Resistance, Enzyme Inhibitors, Humans, Neoplasms, Experimental, drug therapy, Topoisomerase I Inhibitors

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          Abstract

          CPT-11 (irinotecan) is a water-soluble analogue of camptothecin (CPT), an antitumor drug extracted from the Chinese tree Camptotheca acuminata. SN-38 is an active metabolite of CPT-11 that contributes significantly to its activity. The antitumor effects of CPT-11 and SN-38 are exerted through a novel mechanism of action; inhibition of DNA topoisomerase I. CPT-11 and its metabolite have demonstrated potent inhibitory activity against a variety of cancer cell lines in vitro and against several murine and human tumors grafted in mice in vivo, including those that express multidrug resistance. CPT-11 has also shown synergistic activity in combination with 5-fluorouracil and cisplatin in vitro. No irreversible or unusual toxicities were observed with CPT-11 in animal toxicity studies. In summary, the preclinical profile of CPT-11 confirmed this drug to be an attractive candidate for clinical development.

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