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1.
Anticancer Res ; 35(9): 4757-64, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26254366

ABSTRACT

The purpose of the present study was to develop an advanced method of anti-angiogenic chemoembolization to target morphological vascular heterogeneity in tumors and further the therapeutic efficacy of cancer treatment. This new chemoembolization approach was designed using resorbable calcium-phosphate ceramic microspheres (CPMs), in a mixture of three different sizes, which were loaded with an anti-angiogenic agent to target the tumor vasculature in highly angiogenic solid tumors in humans in vivo. The human uterine carcinosarcoma cell line, FU-MMT-3, was used in this study because the tumor is highly aggressive and exhibits a poor response to radiotherapy and chemotherapeutic agents that are in current use. CPMs loaded with TNP-470, an anti-angiogenic agent, were injected into FU-MMT-3 xenografts in nude mice three times per week for 8 weeks. The treatment with TNP-470-loaded CPMs of three different diameters achieved a greater suppression of tumor growth in comparison to treatment with single-size TNP-470-loaded CPMs alone, and the control. Severe loss of body weight was not observed in any mice treated with any size of TNP-470-loaded CPMs. These results suggest that treatment with a mixture of differently-sized anti-angiogenic CPMs might be more effective than treatment with CPMs of a single size. This advanced chemoembolization method, which incorporated an anti-angiogenic agent to target the morphological vascular heterogeneity of tumors may contribute to effective treatment of locally advanced or recurrent solid tumors.


Subject(s)
Angiogenesis Inhibitors/therapeutic use , Calcium Phosphates/therapeutic use , Ceramics/therapeutic use , Chemoembolization, Therapeutic , Microspheres , Neoplasms/blood supply , Neovascularization, Pathologic/drug therapy , Animals , Antineoplastic Agents/therapeutic use , Crystallization , Cyclohexanes/pharmacology , Cyclohexanes/therapeutic use , Humans , Mice, Nude , Microscopy, Electron, Scanning , Neoplasms/drug therapy , Neoplasms/pathology , Neovascularization, Pathologic/pathology , O-(Chloroacetylcarbamoyl)fumagillol , Sesquiterpenes/pharmacology , Sesquiterpenes/therapeutic use , Xenograft Model Antitumor Assays
2.
Cancer Sci ; 101(4): 984-90, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20109162

ABSTRACT

The purpose of the present study was to develop a new method of chemoembolization to improve the therapeutic effectiveness and safety profile of cancer treatment. A chemoembolization approach was designed for human solid tumors using resorbable calcium-phosphate ceramic microspheres loaded with an agent anti-angiogenic to tumor vasculature in vivo. The human uterine sarcoma cell line FU-MMT-3 was used in this study because this tumor is aggressive and also exhibits a poor response to radiotherapy or any chemotherapy currently used. The calcium-phosphate ceramic microspheres loaded with TNP-470, an anti-angiogenic agent, were injected into FU-MMT-3 xenografts in nude mice three times per week for 8 weeks. The treatment using TNP-470-loaded microspheres suppressed tumor growth, compared to treatment with TNP-470 alone, microspheres alone, and the control. The mean tumor weight after treatment using TNP-470-loaded microspheres was significantly lower than that after treatment with microspheres alone. These ceramic microspheres were remarkably embolized in tumor microvessels as well as in the feeding arteries and a significant reduction of intratumoral vascularity was also demonstrated following treatment with TNP-470-loaded microspheres. Severe loss of body weight was not observed in any mice treated with the TNP-470-loaded microspheres, compared to treatment with TNP-470 alone. These results suggest that targeting tumor vasculature in human uterine sarcoma using calcium-phosphate microspheres might be more effective and safer than the treatment that employs anti-angiogenic agent alone. This new chemoembolization method incorporating an anti-angiogenic agent may contribute to the effective treatment of locally advanced or recurrent solid tumors.


Subject(s)
Angiogenesis Inhibitors/therapeutic use , Uterine Neoplasms , Animals , Antineoplastic Agents , Calcium Phosphates , Cell Line, Tumor , Ceramics , Cyclohexanes , Female , Humans , Mice , Mice, Nude , Microspheres , O-(Chloroacetylcarbamoyl)fumagillol , Sesquiterpenes , Uterine Neoplasms/blood supply , Uterine Neoplasms/drug therapy , Uterine Neoplasms/pathology , Xenograft Model Antitumor Assays
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