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1.
Indian J Exp Biol ; 2000 Jun; 38(6): 554-8
Article in English | IMSEAR | ID: sea-60353

ABSTRACT

Damage induction to tumour target cells (P815) by direct electric current (DC) was investigated. A 6 min treatment of P815 cells with DC generated decreased levels of cell viability and proliferation. The ultrastructural analysis of DC-treated cells revealed the presence of blebs, loss of cell surface filopodia, and ruptures in cell membrane. Mitochondrial alterations, swelling of cells, cytoplasmic matrix rarefaction, and cellular debri formation were also observed. The study shows that tumoural target cells can be damaged by direct electric current and this approach may provide means to understand the mechanism of tumour regression induced by electrochemical therapy.


Subject(s)
Animals , Cell Death , Cell Division , Electric Stimulation Therapy , Electricity , Mast-Cell Sarcoma/pathology , Mice , Microscopy, Electron , Tumor Cells, Cultured/ultrastructure
2.
Article in English | IMSEAR | ID: sea-34157

ABSTRACT

Cholangiocarcinoma (CCA) is a relatively rare tumor that occurs primarily in tropical countries and particularly in those with a high incidence of liver fluke infection. A hamster model for a liver fluke-associated CCA has been described previously. In the present study, hamster cholangiocarcinoma cell lines were established and characterized in order to obtain information regarding diagnostically useful tumor marker which could shed light for a future investigation for human cholangiocarcinoma. Two related cell lines, one from the original intrahepatic bile duct tumor and one from an allotransplanted tumor, were established. The established cell lines were found to have population doubling times of 31 and 26 hours respectively, and were maintained in Ham's F12 medium supplemented with 10% fetal bovine serum for over 80 passages. The cell monolayers were subjected to scanning and transmission electron microscopic study and found to have ultrastructural characteristics, including cytoplasmic lumens, consistent with those of adenocarcinoma cells of epithelial origin. An immunoperoxidase study using monoclonal antibodies (MAbs) specific for tumor antigens showed the cytoplasm and membrane of both cell lines to be positive. These antigens were also secreted in soluble form into the culture medium, judging from polyacrylamide gel electrophoresis in the presence of SDS and from immunoblot analyses. Different lines of evidence presented suggested that a 200 kDa glycoprotein produced and secreted by the tumor cell lines could be considered a cholangiocarcinoma-associated marker which has diagnostic potential.


Subject(s)
Animals , Antigens, Neoplasm/analysis , Bile Duct Neoplasms/immunology , Cholangiocarcinoma/immunology , Cricetinae , Disease Models, Animal , Liver Diseases, Parasitic/complications , Mesocricetus , Opisthorchiasis/complications , Thailand , Tumor Cells, Cultured/ultrastructure , Biomarkers, Tumor/analysis
4.
Indian J Exp Biol ; 1990 Dec; 28(12): 1101-6
Article in English | IMSEAR | ID: sea-56128

ABSTRACT

Properties of a transplantable rat histiocytoma which behaves like a macrophage-like cell, have been described. The AK-5 grows as ascites as well as solid subcutaneous tumor. The ascites from one animal can give between 10(8) and 10(9) cells whereas the subcutaneous tumor grows between 20 and 40 cm3 size. These cells possess various degradative enzymes, macrophage markers and glucocorticoid receptors. Beside histopathology the surface topography and ultrastructure of these cells are described.


Subject(s)
Animals , Cell Division , Female , Histiocytoma, Benign Fibrous/ultrastructure , Macrophages/ultrastructure , Male , Rats , Rats, Inbred Strains , Tumor Cells, Cultured/ultrastructure
5.
Acta cient. venez ; 40(4): 246-50, 1989. ilus, tab
Article in Spanish | LILACS | ID: lil-86870

ABSTRACT

Cell membranes of carcinosarcoma-256 ascites cells were isolated by the Zn++ method. Neutral sugars, sialic acid, fucose and N-Acetylhexosamines were determined in the cell membrane fraction. Cells were agglutinated by wheat germ agglutinin, Concanavalin A, and the lectins from Phaseolus vulgaris and Glycine max. No agglutination was observed with peanut lectin (Arachis hypogaea). Gel electrophoresis under dissociting conditions revealed more than 40 bands in the membrane fraction after silver staining. Only 2 bands were evident with PAS stainig


Subject(s)
Rats , Animals , Female , Ascitic Fluid/cytology , Carcinoma 256, Walker/ultrastructure , Cell Fractionation/methods , Tumor Cells, Cultured/ultrastructure , Cell Membrane/ultrastructure , Electrophoresis, Polyacrylamide Gel , Rats, Sprague-Dawley
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