RNA interference-mediated silencing of NANOG leads to reduced proliferation and self-renewal, cell cycle arrest and apoptosis in T-cell acute lymphoblastic leukemia cells via the p53 signaling pathway.

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

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