• Anti-cancer drugs · Mar 2006

    Anti-tumor activity of Titanocene Y in xenografted Caki-1 tumors in mice.

    • Iduna Fichtner, Clara Pampillón, Nigel J Sweeney, Katja Strohfeldt, and Matthias Tacke.
    • aMax Delbrück Center for Molecular Medicine, Berlin, Germany.
    • Anticancer Drugs. 2006 Mar 1; 17 (3): 333-6.

    AbstractThe benzyl-substituted unbridged titanocene bis-[(p-methoxybenzyl)cyclopentadienyl] titanium(IV) dichloride (Titanocene Y) was tested in vitro against human renal cancer cells (Caki-1), in which it showed an IC50 value of 36 x 10 mol/l. Titanocene Y was then given in vivo in doses of 10, 20, 30, 40 and 50 mg/kg on 5 consecutive days to Caki-1-bearing mice, and it showed concentration-dependent and statistically significant tumor growth reduction with respect to a solvent-treated control cohort. The maximum tolerable dose of Titanocene Y was determined to be 40 mg/kg and it showed significantly better tumor volume growth reduction than cisplatin given at a dose of 2 mg/kg. This superior activity of Titanocene Y with respect to cisplatin will hopefully lead to clinical tests against metastatic renal cell cancer in the near future.

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