作者: Nicolle M. Linnerth , Megan D. Siwicky , Craig I. Campbell , Katrina L.M. Watson , James J. Petrik
DOI: 10.1593/NEO.09310
关键词: Cancer research 、 Mammary tumor 、 Insulin-Like Growth Factor Receptor 、 Growth factor receptor 、 Carcinogenesis 、 Transgenic Model 、 Mouse mammary tumor virus 、 Biology 、 Genetically modified mouse 、 Alveolar cells
摘要: Despite the type I insulin-like growth factor receptor (IGF-IR) being highly expressed in more than 80% of human lung tumors, a transgenic model IGF-IR overexpression has not been created. We produced two novel mouse models which is overexpressed either II alveolar cells (surfactant protein C [SPC]-IGFIR) or Clara (CCSP-IGFIR) doxycycline-inducible manner. Overexpression cell caused multifocal adenomatous hyperplasia with papillary and solid adenomas. These tumors thyroid transcription 1 Kruppel-like 5 most tumor cells. Similar to our previous work that developed mammary virus-IGF-II mice, develop SPC-IGFIR CCSP-IGFIR mice high levels cyclic adenosine monophosphate response element binding was localized primarily nucleus. Although elevated expression can initiate development, become independent signaling as down-regulation established regression some, but all, tumors. findings implicate an important initiator tumorigenesis suggest be used further understanding cancer role plays this disease.