Journal
CARCINOGENESIS
Volume 22, Issue 11, Pages 1843-1851Publisher
OXFORD UNIV PRESS
DOI: 10.1093/carcin/22.11.1843
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Rodents exposed to peroxisome proliferator xenobiotics respond with marked increases in hepatocellular replication and growth that results in tumor formation. Recently, tumor necrosis factor-alpha (TNF alpha) was proposed as the central mediator of this maladaptive response. To define the role of TNF alpha signaling in hepatocellular growth induced by peroxisome proliferators we administered three daily gavage doses of the potent peroxisome proliferator, Wy-14 643, to mice nullizygous for TNF-receptor I (TNFR1), TNFR2, or both receptors. We demonstrate here that regardless of genotype the mice responded with almost identical increases in liver to body weight ratios and hepatocyte proliferation. Lacking evidence that TNF alpha signaling mediates these effects, we then examined the possible contribution of alternative cytokine pathways. Semi-quantitative, reverse transcriptase polymerase chain reaction analysis revealed that wild type mice acutely exposed to Wy-14 643 had increased hepatic expression of Il1 beta, Il1r1, Hnf4, and Stat3 genes. Moreover, hepatic adenomas from mice chronically exposed to Wy-14 643 had increased expression of Il1 beta, Il1r1, Il6, and Ppary1. Expression of Il1 alpha, Tnf alpha, Tnfr1, Tnfr2, Ppar alpha, or C/ebp alpha was not altered by acute Wy-14 643 exposure or in adenomas induced by Wy-14643. These data suggest that the hepatic mitogenesis and carcinogenesis associated with peroxisome proliferator exposure is not mediated via TNFa but instead may involve an alternative pathway requiring IL1 beta and IL6.
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