The development of successful models for the initiation and characterization of in vitro transformed epithelial cells is needed since the majority of cancers are of epithelial cell origin. The choice of colon epithelium is based on a number of factors. Large bowel cancer currently represents the highest incidence of all visceral human neoplastic diseases in the United States. However, few in vitro studies have been done using colon or other gastrointestinal epithelia, since no good method to culture these cells was available. Our recent, exciting success in culturing human colon epithelium now allows us to pursue the much-needed in vitro transformation experiments which may help elucidate the mechanism(s) of oncogenesis.
The specific aims of these studies are: (i) to transform human colon epithelial cells with chemical (azoxy-methane) and viral (""""""""oncogene"""""""") carcinogens, (ii) to clone the transformants, then select and propagate stock cultures of several clones for characterization studies, and (iii) to compare characteristics displayed by in vitro transformed cells with normal cells and human colon cancer cells as a prelude to elucidating mechanisms of oncogenesis. Morphology, growth, cytogenetics, viral oncogene expression and cell surface and ionic changes will be assessed. These analyses should determine if specific features associated with colon cancer (e.g., induction of embryonic antigens such as CEA, changes in lectin binding, or expression of the 19-9 gylcolipid colon tumor antigen) occur upon cell transformation or are possibly a later event during cancer progression. The proposed research will also contribute to a better understanding of growth regulation and differentiation of human colon epithelial cells. Such information will provide a foundation for designing biologically relevant approaches to colon cancer diagnosis and therapy.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Unknown (R23)
Project #
1R23CA035933-01A2
Application #
3446493
Study Section
Chemical Pathology Study Section (CPA)
Project Start
1985-01-01
Project End
1987-12-31
Budget Start
1985-01-01
Budget End
1985-12-31
Support Year
1
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Texas Health Science Center San Antonio
Department
Type
Schools of Medicine
DUNS #
800772162
City
San Antonio
State
TX
Country
United States
Zip Code
78229
Moyer, M P; Konyecsni, W M; Stauffer, J S et al. (1988) Colon cell transformation as an in vitro model of premalignancy. Prog Clin Biol Res 279:363-72
Moyer, M P; Aust, J B (1987) Phenotypic changes and gene expression in human colon mucosal epithelial cells upon transfection of a SV40 DNA-gpt recombinant. In Vitro Cell Dev Biol 23:141-6
Moyer, M P; Dixon, P S; Rothman, S W et al. (1987) Cytotoxicity of Shiga toxin for primary cultures of human colonic and ileal epithelial cells. Infect Immun 55:1533-5
Moyer, M P; Armstrong, A; Aust, J B et al. (1986) Effects of gastrin, glutamine, and somatostatin on the in vitro growth of normal and malignant human gastric mucosal cells. Arch Surg 121:285-8
Moyer, M P; Aust, J B; Dixon, P S et al. (1985) Glucagon enhances growth of cultured human colorectal cancer cells in vitro. Am J Surg 150:676-9