mortality/aging
• mice are resistant to LPS/D-galactosamine lethality
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• in mice treated with AOM/DSS
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digestive/alimentary system
• in mice treated with AOM/DSS
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• decreased in mice treated with AOM/DSS
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• increased in mice treated with AOM/DSS
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• high-grade dysplasia in mice treated with AOM/DSS
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• decreased colon length in mice treated with AOM/DSS
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neoplasm
• increased number and size of macroscopically visible tumors in mice treated with AOM/DSS
• however, treatment with only AOM does not alter tumor formation and inhibition of c-Met activation alleviates tumor promotion
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• increased number of macroscopically visible tumors in mice treated with AOM/DSS
• however, treatment with only AOM does not alter tumor formation
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cardiovascular system
• in mice treated with AOM/DSS
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growth/size/body
• in mice treated with AOM/DSS
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homeostasis/metabolism
• mice are resistant to LPS/D-galactosamine lethality
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• in mice treated with AOM/DSS
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• mice treated with AOM/DSS exhibit increased weight loss, decreased survival, increased disease index (diarrhea and rectal bleeding scores), high-grade colon dysplasia, decreased colon length and increased size and number of macroscopically visible tumors compared with wild-type mice
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• increased number and size of macroscopically visible tumors in mice treated with AOM/DSS
• however, treatment with only AOM does not alter tumor formation and inhibition of c-Met activation alleviates tumor promotion
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immune system
• in peritoneal macrophages tested with LPS
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cellular
• decreased in mice treated with AOM/DSS
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• increased in mice treated with AOM/DSS
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