PI3K/AKT/mTOR通路
鼻咽癌
SOX2
癌症研究
体内
干细胞
生物
细胞生长
胚胎干细胞
癌症干细胞
细胞生物学
信号转导
医学
内科学
生物化学
生物技术
基因
放射治疗
遗传学
作者
Chunguang Yang,Jianhua Peng,WenJing Jiang,Yue Zhang,Xiaoyun Chen,Xianmin Wu,Yi Zhu,Huxiang Zhang,Jian‐Fu Chen,Jixian Wang,William C. Cho,Kunlin Jin
出处
期刊:Cancer Letters
[Elsevier]
日期:2013-08-07
卷期号:341 (2): 186-194
被引量:19
标识
DOI:10.1016/j.canlet.2013.08.004
摘要
The mammalian target of rapamycin (mTOR) signaling is a key pathway in the progression of different cancers and in the homeostasis of stem cells. Here, we investigated the link between mTOR signaling and cancer stem cells (CSCs) in nasopharyngeal carcinoma (NPC). We found that human primary NPC expressed embryonic stem cell (ESC) markers: CD133, SOX2 and OCT4 as well as pmTOR and pS6. Primary ESC-positive NPC cells could form secondary NPC in BALB/c nude mice. Rapamycin, an mTOR inhibitor, significantly suppressed ESC-positive NPC cell growth in vitro and tumor formation in vivo. Our findings suggest that mTOR signaling is activated in CSC-like cells and plays an important role in NPC growth.
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