immune system
• in the liver of DEN-treated mice
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• in the liver and peripheral blood of DEN-treated mice
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neoplasm
• DEN-treated mice develop smaller hepatocellular carcinoma with greater latency compared with wild-type mice
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• in DEN-treated mice
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homeostasis/metabolism
• DEN-treated mice develop smaller hepatocellular carcinoma with greater latency compared with wild-type mice
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• during early tumor promotion, diethylnitrosamine (DEN)-treated mice exhibit reduced liver damage and compensatory proliferation compared with wild-type mice
• however, adoptive transfer of wild-type Kupffer cells reverses unresponsiveness to DEN-induced liver injury
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hematopoietic system
• in the liver of DEN-treated mice
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• in the liver and peripheral blood of DEN-treated mice
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