Abstract | BACKGROUND/AIM:
Titanocene dichloride held great promise as a chemotherapeutic compound in pre-clinical studies. However, subsequent clinical trials revealed hepatoxicity and nephrotoxicity, which limited its use in clinical applications. Therefore, we used steroid pendant groups to improve the targeting of titanocene in MCF-7 breast cancer cells, and demonstrated a 10-fold lower effective dose compared to titanocene in in vitro assays. The aim of the present study was to test the efficacy of a titanocene functionalized with pregnenolone (Ti-Preg) in an in vivo breast cancer model. MATERIALS AND METHODS: Xenografts from the MCF7 breast cancer cell line were implanted into athymic nu/nu mice to evaluate the potential of Ti-Preg as an anti- breast cancer agent. RESULTS: Ti-Preg demonstrated significant inhibition of MCF-7 tumor growth when compared to vehicle and to titanocene controls. CONCLUSION:
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Authors | Gladiany Ramos, Yaliz Loperena, Giovanni Ortiz, Fiorella Reyes, Ada Szeto, Jose Vera, Javier Velez, Jessica Morales, Deborah Morrero, Linnette Castillo, Surangani Dharmawardhane, Enrique Melendez, A Valance Washington |
Journal | Anticancer research
(Anticancer Res)
Vol. 34
Issue 4
Pg. 1609-15
(Apr 2014)
ISSN: 1791-7530 [Electronic] Greece |
PMID | 24692689
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- Antineoplastic Agents
- Organometallic Compounds
- Pregnenolone
- titanocene dichloride
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Topics |
- Animals
- Antineoplastic Agents
(administration & dosage, chemistry, pharmacology)
- Cell Line, Tumor
- Cell Proliferation
(drug effects)
- Drug Synergism
- Female
- Humans
- Kidney
(drug effects, pathology)
- Liver
(drug effects, pathology)
- MCF-7 Cells
- Mice
- Organometallic Compounds
(administration & dosage, chemistry, pharmacology)
- Pregnenolone
(administration & dosage, chemistry, pharmacology)
- Tumor Burden
(drug effects)
- Xenograft Model Antitumor Assays
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