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      Antitumor activity of TZT-1027 (Soblidotin).

      Anticancer research
      ATP-Binding Cassette Transporters, biosynthesis, metabolism, Animals, Antineoplastic Agents, pharmacokinetics, pharmacology, Cell Death, drug effects, physiology, Cell Growth Processes, Cell Line, Tumor, Colonic Neoplasms, drug therapy, pathology, DNA Fragmentation, Drug Resistance, Multiple, Drug Resistance, Neoplasm, Drug Screening Assays, Antitumor, Fibrosarcoma, Humans, Male, Mice, Mice, Inbred BALB C, Multidrug Resistance-Associated Proteins, Neoplasm Proteins, Oligopeptides, P-Glycoprotein, Xenograft Model Antitumor Assays

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          Abstract

          TZT-1027 (Soblidotin), a newly synthesized dolastatin 10 derivative that depolymerizes microtubules, has potent antitumor activity. Cell-killing kinetic analysis was performed by the colony-forming assay and the kinetics of TZT-1027 were compared with those of neocarzinostatin, adriamycin and vincristine, known to be typical concentration-, AUC- and time-dependent agents, respectively. DNA fragmentation was detectable by electrophoresis, cytotoxicity was evaluated by MTT assay and antitumor activity was examined by measuring the tumor weight after treatment. TZT-1027 exhibited its cytocidal and apoptosis-inducing activity in a time-dependent manner. Its growth-inhibitory effect was less affected by overexpression of P-glycoprotein than that of other tubulin inhibitors and was not affected by the overexpression of breast cancer resistance protein or multidrug resistance-associated protein. TZT-1027 exhibited potent antitumor activities in an in vivo tumor model in which vincristine and docetaxel failed to show effectiveness. Because its growth-inhibitory and antitumor activities were superior to those of the other drugs tested, including the tubulin inhibitors paclitaxel, docetaxel and vincristine, TZT-1027 should be useful in the chemotherapy of tumors that are not responsive to other tubulin inhibitors.

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