作者: Jiang Cao , Li Li , Chong Chen , Chao Lv , Fanjing Meng
DOI: 10.1016/J.LEUKRES.2013.04.021
关键词:
摘要: NANOG is critical for maintaining the self-renewal and proliferative properties of embryonic stem cells. Here we found that cultured T-cell acute lymphoblastic leukemia (T-ALL) cells, as well human primary T-ALL express a functional variant NANOG. mRNA derived predominantly from retrogene locus termed NANOGP8. Furthermore, showed RNA interference-mediated knockdown inhibited cell proliferation, reduced self-renewal, promoted apoptosis arrested cycle through p53-mediated pathway in leukemic These findings demonstrate oncogenic potential this pluripotent gene