Cancer stem-like side population cells in the human nasopharyngeal carcinoma cell line CNE-2 possess epithelial mesenchymal transition properties in association with metastasis

被引:34
作者
Guo, Dan [1 ]
Xu, Ben-Ling [2 ]
Zhang, Xu-Hua [2 ]
Dong, Ming-Min [1 ]
机构
[1] Zhengzhou Univ, Dept Otolaryngol Head & Neck Surg, Affiliated Hosp 1, Zhengzhou 450052, Henan, Peoples R China
[2] Zhengzhou Univ, Dept Biotherapy, Lab Ctr, Affiliated Canc Hosp, Zhengzhou 450008, Henan, Peoples R China
关键词
nasopharyngeal carcinoma; cancer stem cells; epithelial-mesenchymal transition; metastasis; TRANSCRIPTIONAL REGULATION; PROSPECTIVE IDENTIFICATION; EXPRESSION; COMPLEX; NANOG; OCT4; HEAD;
D O I
10.3892/or.2012.1781
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
It has been recently reported that side population (SP) cells in nasopharyngeal carcinoma (NPC) cell lines display characteristics of cancer stem-like cells. However, the biological behavior and the significance of these cells for NPC progression remain unclear. In this study, we isolated SP cells from the NPC cell line CNE-2 by flow cytometry and investigated their biological characteristics. We discovered that SP cells had stronger colony forming abilities compared to the non-side population (NSP) cells, and observed that some SP cells looked more like the shape of mesenchymal cells when cultured in the common polyHEMA-coated flask. When checked by quantitative real-time PCR, the SP cells expressed higher levels of sternness-related genes Oct4, Sox2 and Nanog, and mesenchymal cell-related genes N-cadherin, vimentin and Snail, while they expressed lower levels of the epithelial cell-related gene, E-cadherin. Western blot and immunofluorescence staining methods further verified that SP cells expressed higher vimentin and expressed lower E-cadherin levels. Finally, Transwell invasion assay results indicated that the SP cells had higher invasive potential compared to NSP cells. Collectively, our data reveal that SP cells in the CNE-2 cell line not only possess the properties of cancer stem cells, but also have more mesenchymal cell characteristics which are associated with epithelial mesenchymal transition (EMT) and cancer cell invasion and metastasis. These findings are helpful for developing novel targets for effective clinical treatment of NPC.
引用
收藏
页码:241 / 247
页数:7
相关论文
共 30 条
[1]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[2]   Functional and molecular characterisation of mammary side population cells [J].
Alvi, Azra J. ;
Clayton, Helen ;
Joshi, Chirag ;
Enver, Tariq ;
Ashworth, Alan ;
Vivanco, Maria d M. ;
Dale, Trevor C. ;
Smalley, Matthew J. .
BREAST CANCER RESEARCH, 2002, 5 (01)
[3]   Core transcriptional regulatory circuitry in human embryonic stem cells [J].
Boyer, LA ;
Lee, TI ;
Cole, MF ;
Johnstone, SE ;
Levine, SS ;
Zucker, JR ;
Guenther, MG ;
Kumar, RM ;
Murray, HL ;
Jenner, RG ;
Gifford, DK ;
Melton, DA ;
Jaenisch, R ;
Young, RA .
CELL, 2005, 122 (06) :947-956
[4]  
Chao C, 2011, PLOS ONE, V6
[5]   Reciprocal transcriptional regulation of Pou5f1 and Sox2 via the Oct4/Sox2 complex in embryonic stem cells [J].
Chew, JL ;
Loh, YH ;
Zhang, WS ;
Chen, X ;
Tam, WL ;
Yeap, LS ;
Li, P ;
Ang, YS ;
Lim, B ;
Robson, P ;
Ng, HH .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (14) :6031-6046
[6]   Prospective identification of tumorigenic prostate cancer stem cells [J].
Collins, AT ;
Berry, PA ;
Hyde, C ;
Stower, MJ ;
Maitland, NJ .
CANCER RESEARCH, 2005, 65 (23) :10946-10951
[7]   Isolation and functional properties of murine hematopoietic stem cells that are replicating in vivo [J].
Goodell, MA ;
Brose, K ;
Paradis, G ;
Conner, AS ;
Mulligan, RC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (04) :1797-1806
[8]  
Hay ED, 1995, ACTA ANAT, V154, P8
[9]   Distinct populations of cancer stem cells determine tumor growth and metastatic activity in human pancreatic cancer [J].
Hermann, Patrick C. ;
Huber, Stephan L. ;
Herrler, Tanja ;
Aicher, Alexandra ;
Ellwart, Joachim W. ;
Guba, Markus ;
Bruns, Christiane J. ;
Heeschen, Christopher .
CELL STEM CELL, 2007, 1 (03) :313-323
[10]   Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method [J].
Livak, KJ ;
Schmittgen, TD .
METHODS, 2001, 25 (04) :402-408