transforming growth Factor α (TGF-α) has been shown to induce liver tumors within 1 year in transgenic male mice in which this potent mitogen is overexpressed. To determine more precisely how TGF-α participates in multistep tumorigenesis of the liver, genotoxic (diethylnitrosamine or di-methylnitrosamine) and nongenotoxic (phenobarbital) chemical carcinogens were administered independently to TGF-α transgenic mice [line MT42 on a Crl:CD-l(ICR)BR background]. TGF-α overexpression dramatically accelerated carcinogen-induced hepatocarcinogenesis in MT42 males but not females. Interestingly, all three chemical agents were found to enhance strongly both hepatic tumor formation and progression in TGF-α transgenic male mice. In this study 100%, 90%, and 78% of transgenic males exposed to diethylnitrosamine, dimethylnitrosamine or phenobarbital, respectively, developed tumors between 24 and 32 weeks of age. Moreover, approximately 70% of tumor-bearing transgenic mice from each treatment group had hepatocellular carcinomas; no malignant lesions were found in any carcinogen-treated or untreated nontransgenic mice or in untreated MT42 mice at this age. These results demonstrate that chemical agents as diverse as nitrosamines and phenobarbital act as cocarcinogens with TGF-α in the livers of these transgenic mice, indicating that TGF-α possesses the unique ability to complement both initiation and promotion in hepatocarcinogenesis. Furthermore, because carcinogen-induced malignant conversion was restricted to transgenic mice, constitutive TGF-α overexpression may promote liver tumor progression as well.
|Original language||English (US)|
|Number of pages||8|
|State||Published - Sep 1993|
ASJC Scopus subject areas
- Cancer Research