mTOR activation in immature cells of primary nasopharyngeal carcinoma and anti-tumor effect of rapamycin in vitro and in vivo

被引:22
|
作者
Yang, Chunguang [1 ]
Peng, Jianhua [1 ]
Jiang, WenJing [1 ]
Zhang, Yue [1 ]
Chen, Xiaoyun [1 ]
Wu, Xianmin [1 ]
Zhu, Yi [1 ]
Zhang, Huxiang [2 ]
Chen, Jianfu [1 ]
Wang, Jixian [4 ]
Cho, William C. S. [3 ]
Jin, Kunlin [1 ,4 ]
机构
[1] Wenzhou Med Coll, Affiliated Hosp 1, Dept Otolaryngol, Wenzhou 325000, Zhejiang, Peoples R China
[2] Wenzhou Med Coll, Affiliated Hosp 1, Dept Pathol, Wenzhou 325000, Zhejiang, Peoples R China
[3] Queen Elizabeth Hosp, Dept Clin Oncol, Kowloon, Hong Kong, Peoples R China
[4] Univ North Texas Hlth Sci Ctr Ft Worth, Dept Pharmacol & Neurosci, Ft Worth, TX 76107 USA
关键词
Cancer stem cells; Nasopharyngeal carcinoma; mTOR signaling; Rapamycin; GROWTH-FACTOR RECEPTOR; BREAST-CANCER; RIBOSOMAL-PROTEIN; SIGNALING PATHWAY; STEM-CELLS; EXPRESSION; IDENTIFICATION; MARKER; PHOSPHORYLATION; RESISTANCE;
D O I
10.1016/j.canlet.2013.08.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:186 / 194
页数:9
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