作者: Kate D. Sutherland , Natalie Proost , Inge Brouns , Dirk Adriaensen , Ji-Ying Song
DOI: 10.1016/J.CCR.2011.04.019
关键词:
摘要: Small cell lung cancer (SCLC) is one of the most lethal human malignancies. To investigate cellular origin(s) this cancer, we assessed effect Trp53 and Rb1 inactivation in distinct types adult using adenoviral vectors that target Cre recombinase to Clara, neuroendocrine (NE), alveolar type 2 (SPC-expressing) cells. Using these type-restricted Adeno-Cre viruses, show loss can efficiently transform NE SPC-expressing cells leading SCLC, albeit at a lesser efficiency. In contrast, Clara were largely resistant transformation. The results indicate although serve as predominant origin SCLC subset are also endowed with ability.