Intravital Microscopic Characterization of Suramin Effects in an Orthotopic Immunocompetent Rat Model of Pancreatic Cancer
Autor: | Hubert G. Hotz, Heinz J. Buhr, Birgit Hotz |
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Rok vydání: | 2008 |
Předmět: |
Pathology
medicine.medical_specialty Suramin Rat model Angiogenesis Inhibitors Antineoplastic Agents Vascular permeability Microcirculation Capillary Permeability Cell Line Tumor Pancreatic cancer Tumor Cells Cultured Animals Medicine Tumor growth Cell Proliferation Microscopy Video business.industry Cell growth Gastroenterology medicine.disease Rats Pancreatic Neoplasms Rats Inbred Lew Surgery business Neoplasm Transplantation Intravital microscopy Carcinoma Pancreatic Ductal medicine.drug |
Zdroj: | Journal of Gastrointestinal Surgery. 12:900-906 |
ISSN: | 1873-4626 1091-255X |
DOI: | 10.1007/s11605-008-0507-x |
Popis: | We investigated the effect of suramin on tumor growth and spread in an immunocompetent, orthotopic rat model of pancreatic cancer and analyzed the tumor vasculature by intravital microscopy.In vitro, rat ductal pancreatic cancer cells (DSL-6A) were incubated with suramin (10-800 microg/ml), and cell proliferation was assessed. In vivo, DSL-6A tumors were induced in the pancreas of Lewis rats. Animals received suramin (60 mg/kg, weekly i.p.) or the vehicle (controls). Treatment started after 3 days. Intravital microscopy after 1, 4, and 8 weeks quantified diameter, density, and permeability of tumor vessels. Primary tumor volume, local infiltration, and metastatic spread were determined at autopsy. Microvessel density was analyzed by immunohistochemistry.In vitro, proliferation was inhibited by suramin up to 95%. In vivo, all controls developed extensive tumor growth and spread. No tumor was detectable in half of the suramin-treated animals after 8 weeks; tumor dissemination was almost completely depressed. Suramin therapy resulted in a complete regression of tumor macrovessels and a significant reduction of microvessel density.Suramin significantly reduces primary tumor growth and dissemination in a clinically relevant rat model of pancreatic cancer and seems to play an important role for the inhibition of tumor angiogenesis. |
Databáze: | OpenAIRE |
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