TY - JOUR
T1 - In vitro tramsformation of rat bladder epithelium by 2-amino-4-(5-nitro-2-furyl)thiazole
AU - Mann, Angela M.
AU - Masui, Tsuneo
AU - Chlapowski, Frank J.
AU - Okamura, Takehiko
AU - Borgeson, Claudia D.
AU - Cohen, Samuel M.
N1 - Funding Information:
We gratefully acknowledge Mario Stevenson for helpful criticism, and the assistance of Ginni Philbrick and Deboraha Coleman in the preparation of this manuscript. This work was supported in part by USPHS grants CA32513, AM 32937 and CA36727 from the National Institutes of Health.
PY - 1991/3
Y1 - 1991/3
N2 - To establish a rat urinary bladder carcinogenesis model in vitro, primary rat bladder epithelial cells were grown in media containing 2-amino-4(5-nitro-2-furyl)thiazole (ANFT), the water-soluble metabolite of N-[4-(5-nitro-2-furyl)-2-thiazolyl]-formamide (FANFT), for 4 weeks followed by longterm (4-7 months) exposure to control medium, sodium saccharin (NaS), or urea. Another set of cultures were exposed to ANFT, NaS and urea simultaneously. Several phenotypic changes were observed in the chemically exposed cell cultures, namely differences in cell morphology, increased growth rate and the ability to grow on plastic instead of rattail collagen support. All of the chemically exposed cultures were anchorage independent except one of those treated with NaS. The ANFT-treated cells followed by control medium or urea and cells treated with ANFT, NaS and urea were tumorigenic when transplanted to nude mice, whereas NaS or ANFT followed by NaS treatment were not. The tumors were carcinomas and their epithelial differentiation was verified by strong positive staining for cytokeratin. These studies demonstrate the urothelial transforming capability of ANFT in cell culture without the necessity for a long exposure to a secondary chemical.
AB - To establish a rat urinary bladder carcinogenesis model in vitro, primary rat bladder epithelial cells were grown in media containing 2-amino-4(5-nitro-2-furyl)thiazole (ANFT), the water-soluble metabolite of N-[4-(5-nitro-2-furyl)-2-thiazolyl]-formamide (FANFT), for 4 weeks followed by longterm (4-7 months) exposure to control medium, sodium saccharin (NaS), or urea. Another set of cultures were exposed to ANFT, NaS and urea simultaneously. Several phenotypic changes were observed in the chemically exposed cell cultures, namely differences in cell morphology, increased growth rate and the ability to grow on plastic instead of rattail collagen support. All of the chemically exposed cultures were anchorage independent except one of those treated with NaS. The ANFT-treated cells followed by control medium or urea and cells treated with ANFT, NaS and urea were tumorigenic when transplanted to nude mice, whereas NaS or ANFT followed by NaS treatment were not. The tumors were carcinomas and their epithelial differentiation was verified by strong positive staining for cytokeratin. These studies demonstrate the urothelial transforming capability of ANFT in cell culture without the necessity for a long exposure to a secondary chemical.
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U2 - 10.1093/carcin/12.3.417
DO - 10.1093/carcin/12.3.417
M3 - Article
C2 - 2009588
AN - SCOPUS:0025760862
SN - 0143-3334
VL - 12
SP - 417
EP - 422
JO - Carcinogenesis
JF - Carcinogenesis
IS - 3
ER -