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Merck

Dual-action combination therapy enhances angiogenesis while reducing tumor growth and spread.

Cancer cell (2015-01-15)
Ping-Pui Wong, Fevzi Demircioglu, Essam Ghazaly, Wasfi Alrawashdeh, Michael R L Stratford, Cheryl L Scudamore, Biancastella Cereser, Tatjana Crnogorac-Jurcevic, Stuart McDonald, George Elia, Thorsten Hagemann, Hemant M Kocher, Kairbaan M Hodivala-Dilke
ZUSAMMENFASSUNG

Increasing chemotherapy delivery to tumors, while enhancing drug uptake and reducing side effects, is a primary goal of cancer research. In mouse and human cancer models in vivo, we show that coadministration of low-dose Cilengitide and Verapamil increases tumor angiogenesis, leakiness, blood flow, and Gemcitabine delivery. This approach reduces tumor growth, metastasis, and minimizes side effects while extending survival. At a molecular level, this strategy alters Gemcitabine transporter and metabolizing enzyme expression levels, enhancing the potency of Gemcitabine within tumor cells in vivo and in vitro. Thus, the dual action of low-dose Cilengitide, in vessels and tumor cells, improves chemotherapy efficacy. Overall, our data demonstrate that vascular promotion therapy is a means to improve cancer treatment.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
(±)-Verapamil -hydrochlorid, ≥99% (titration), powder
Sigma-Aldrich
2′-Desoxycytidin, ≥99% (HPLC)
USP
Verapamil -hydrochlorid, United States Pharmacopeia (USP) Reference Standard
Supelco
Verapamil hydrochloride solution, 1.0 mg/mL in methanol (as free base), ampule of 1 mL, certified reference material, Cerilliant®
Supelco
(±)-Verapamil -hydrochlorid, Pharmaceutical Secondary Standard; Certified Reference Material
Verapamilhydrochlorid, European Pharmacopoeia (EP) Reference Standard