Molecular Carcinogenesis. 2006 Apr 30; [Epub ahead of print] [Link]
Barbara Kroczynska *, Michele Carbone
Department of Pathology, Cardinal Bernardin Cancer Center, Loyola University Chicago, Maywood, Illinois
*Correspondence to Barbara Kroczynska, Department of Pathology, Cardinal Bernardin Cancer Center, Loyola University Chicago, 2160 South First Avenue, Maywood, IL 60153
The aim of this study was to test the possibility of using human antibodies to study the pathogenic mechanism of SV40 and asbestos in a hamster mesothelioma model. The cellular lysates from human and hamster primary mesothelial cells were tested by Western blot analysis. All of the antibodies we tested (HGF, Notch, VEGF, Sp1, p53, PP2A, p-ERK1, p-c-jun, Fra1, Fra2, MMP1, MMP9, NFkappaB p65, IkappaB, GAPDH) cross-reacted with their hamster counterparts. These data indicate that hamster mesothelioma model and more in general hamster experimental model, can be used for functional studies because many mouse, rabbit, and goat monoclonal antibodies prepared against human antigens cross-react with their hamster counterparts.
Keywords: asbestos, mesothelial cells, mesothelioma, SV40