| Literature DB >> 21822053 |
Kwon-Sik Park1, Mei-Chih Liang, David M Raiser, Raffaella Zamponi, Rebecca R Roach, Stephen J Curtis, Zandra Walton, Bethany E Schaffer, Caitlin M Roake, Anne-Flore Zmoos, Christina Kriegel, Kwok-Kin Wong, Julien Sage, Carla F Kim.
Abstract
Small cell lung carcinoma (SCLC) is a neuroendocrine subtype of lung cancer that affects more than 200,000 people worldwide every year with a very high mortality rate. Here, we used a mouse genetics approach to characterize the cell of origin for SCLC; in this mouse model, tumors are initiated by the deletion of the Rb and p53 tumor suppressor genes in the lung epithelium of adult mice. We found that mouse SCLCs often arise in the lung epithelium, where neuroendocrine cells are located, and that the majority of early lesions were composed of proliferating neuroendocrine cells. In addition, mice in which Rb and p53 are deleted in a variety of non-neuroendocrine lung epithelial cells did not develop SCLC. These data indicate that SCLC likely arises from neuroendocrine cells in the lung.Entities:
Mesh:
Substances:
Year: 2011 PMID: 21822053 PMCID: PMC3219544 DOI: 10.4161/cc.10.16.17012
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534