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Caption | Drug treatment of mammary carcinomas in Eef1a1tm1(Kras*)Arge/Eef1a1+ Waptm1(cre)Arge/Wap+ mice. (A) Examples of gross anatomical examination of tumors that developed in mice carrying an activated Kras* oncogenic transgene (Eef1a1tm1(Kras*)Arge/Eef1a1+ Waptm1(cre)Arge/Wap+) after 3 weeks of treatment either with vehicle (V) or with picropodophyllin (P). (B) Histological examination of the tumors shows that in comparison with the controls (V), the PPP-treated tumors are dramatically smaller (P; dotted circles). (C) Compared with vehicle injections (V), administration of PPP for 3 days (P) increases ~9-fold the level of apoptosis detected in the pale component, as assayed by activated caspase 3 immunohistochemistry brown staining. (D) Comparison of the effects on the components of Kras*-induced carcinomas between PPP administration (P) and vehicle injections (V) for 3 weeks. The PPP treatment diminishes the size of pale cell tumors (dotted circles) and results in extensive keratinization and vacuolation (Inset) of the squamous component. The sarcomatous component remaining after treatment might be overestimated, because it exhibits variable degrees of degenerate changes that are difficult to quantitate, including replacement fibrosis (increased matrix and collagen deposition and proliferation of Fosl1-negative myofibroblasts). (Scale bar, 0.5 cm.) (Magnification: C, D, 400X; C Inset, D Inset, 100X.) | ||||||
Copyright | This image is from Klinakis A, Proc Natl Acad Sci U S A 2009 Feb 17;106(7):2359-64. Copyright 2009 National Academy of Sciences, U.S.A. J:146290 | ||||||
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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 11/12/2024 MGI 6.24 |
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