Antitumor Activity of an Enzyme Prodrug Therapy Targeted to the Breast Tumor Vasculature
Brent D. Van Rite, John J. Krais, Mohamad Cherry, Vassilios I. Sikavitsas, Carla Kurkjian, Roger G. Harrison
Abstract
Brent D. Van Rite, John J. Krais, Mohamad Cherry, Vassilios I. Sikavitsas, Carla Kurkjian, Roger G. Harrison
Abstract
The L-methioninase-annexin V/selenomethionine enzyme prodrug system, designed to target the tumor vasculature and release the methylselenol anticancer drug in the tumor, was tested in mice with implanted MBA-MB-231 breast tumors. This therapy was able to cause a reduction in the size of the tumors during the treatment period. It was shown that L-methioninase-annexin V was uniformly bound at the blood vessel surface in the tumor and also that there was a substantial cutoff of blood flowing through the treated tumor, consistent with the therapy's design. This new approach for enzyme prodrug therapy of breast cancer appears promising.
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The L-methioninase-annexin V/selenomethionine enzyme prodrug system, designed to target the tumor vasculature and release the methylselenol anticancer drug in the tumor, was tested in mice with implanted MBA-MB-231 breast tumors. This therapy was able to cause a reduction in the size of the tumors during the treatment period. It was shown that L-methioninase-annexin V was uniformly bound at the blood vessel surface in the tumor and also that there was a substantial cutoff of blood flowing through the treated tumor, consistent with the therapy's design. This new approach for enzyme prodrug therapy of breast cancer appears promising.
Key concepts: Prodrug, Breast cancer, Annexin, Medicine, Enzyme, Cancer research, Pharmacology, Drug