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Caption | Fen1tm3.1Bhsh/Fen1tm3.1Bhsh (ED) mice are highly susceptible to cancers as a result of their mutator phenotype and chronic inflammation. (a) Chronic inflammation and tumorigenesis in the lung. Top, disease incidence at specific life stages (timeline in months) of wild-type (WT), Fen1tm3.1Bhsh/Fen1+ (ED/+) and Fen1tm3.1Bhsh/Fen1tm3.1Bhsh (ED/ED) mice. Below, histology (H&E) of normal lung, lung with chronic inflammation, adenoma and adenocarcinoma in homozygous mutant mice. The occurrence of chronic pulmonary inflammation was evaluated in the mouse population at 9-12 months. None of the mice had lung tumors at that time. *P = 0.14 and **P = 0.011, two-tailed Fisher's exact test. The percentage incidence of pulmonary neoplasia is as compared to that in mice at ages 14-20 months. Scale bar, 100 um. | ||||
Copyright | This image is from Zheng L, Nat Med 2007 Jul;13(7):812-9 and is displayed with the permission of The Nature Publishing Group who owns the Copyright. J:231218 | ||||
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Associated Genotypes |
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 12/10/2024 MGI 6.24 |
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