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Small cell lung cancer (SCLC) is a highly aggressive human tumor with a more
than 95% mortality rate. Its ontogeny and molecular pathogenesis remains poorly
understood. We established a mouse model for neuroendocrine (NE) lung tumors by
conditional inactivation of Rb1 and Trp53 in mouse lung epithelial cells. Mice
carrying conditional alleles for both Rb1 and Trp53 developed with high
incidence aggressive lung tumors with striking morphologic and immunophenotypic
similarities to SCLC. Most of these tumors, which we designate MSCLC (murine
small cell lung carcinoma), diffusely spread through the lung and gave rise to
extrapulmonary metastases. In our model, inactivation of both Rb1 and p53 was a
prerequisite for the pathogenesis of SCLC.