Autor: |
Anthony Deally, Iduna Fichtner, Matthias Tacke, Wolfgang Walther, Megan Hogan |
Rok vydání: |
2013 |
Předmět: |
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Zdroj: |
Letters in Drug Design & Discovery. 10:375-381 |
ISSN: |
1570-1808 |
DOI: |
10.2174/1570180811310050002 |
Popis: |
The indole-substituted titanocene dichloride derivative Titanocene T, which is completely water-soluble and shows micromolar activity against the human renal cancer cells Caki-1, was tested in vivo an against xenografted human renal cell tumors in mice. Titanocene T was then given at 25 and 50 mg/kg, seven times every four days during three weeks to two groups (n=6) of Caki-1 tumor-bearing female NMRI: nu/nu mice, while the control group was treated with solvent only. At both doses Titanocene T induced a moderate to good tumor growth reduction with respect to the solvent-treated control group, with an optimal T/C value of 51% and 32% and showed neither mortality nor toxicity. Immunohistochemical analysis revealed that the expression of the proliferation marker Ki-67 was reduced in the high-dosage group. Furthermore, anti-angiogenic activity was identified by CD31 staining; the number of micro vessels in a defined tumor area decreased by 27% and 29% due to Titanocene T treatment. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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