Cooperation of side population cells with CD133 to enrich cancer stem cells in a laryngeal cancer cell line

被引:3
作者
Wu, Chun-Ping [1 ]
Xie, Ming [1 ]
Zhou, Liang [1 ]
Tao, Lei [1 ]
Zhang, Ming [1 ]
Tian, Jie [2 ]
机构
[1] Fudan Univ, Dept Otolaryngol Head & Neck Surg, Affiliated Eye Ear Nose & Throat Hosp, Shanghai 200433, Peoples R China
[2] Fudan Univ, Res Ctr, Affiliated Eye Ear Nose & Throat Hosp, Shanghai 200433, Peoples R China
来源
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK | 2014年 / 36卷 / 09期
基金
中国国家自然科学基金;
关键词
side population cells; AC133; antigen; neoplastic stem cells; laryngeal neoplasms; human epithelial type-2 (Hep-2) cell line; INITIATING CELLS; IDENTIFICATION; EXPRESSION; MARKER;
D O I
10.1002/hed.23447
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background. The identification of cancer stem cells (CSCs) in laryngeal cancer remains a dilemma. Our previous studies identified CD133(+) subgroup and side population (SP) cells in the laryngeal cancer cell line, human epithelial type-2 (Hep-2). Although both cell types shared some tumor-initiating properties, they were heterogeneous. In this study, we further enriched CSCs from this cell line. Methods. We divided the SP cells into CD133(+) SP and CD133(-) SP cells by combining SP and CD133, and compared CSC-associated properties between the 2 subgroups. Results. SP cells contained CD133(+) SP and CD133(-) SP, and CD133(+) SP cells manifested preferential expression of self-renewal genes, higher capacity for proliferation, differentiation, and clone and spheroid formation, enhanced resistance to radiation and chemotherapy, and greater tumorigenicity compared with CD133(-) SP cells. Conclusion. The CD133(+) SP subpopulation is enriched in CSCs compared with the CD133(-) SP subgroup, suggesting that the combination of SP and CD133 can further purify CSCs in the Hep-2 cell line. (C) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:1279 / 1287
页数:9
相关论文
共 28 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]   The utility and limitations of glycosylated human CD133 epitopes in defining cancer stem cells [J].
Bidlingmaier, Scott ;
Zhu, Xiaodong ;
Liu, Bin .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2008, 86 (09) :1025-1032
[3]   Side Population is Not Necessary or Sufficient for a Cancer Stem Cell Phenotype in Glioblastoma Multiforme [J].
Broadley, Kate W. R. ;
Hunn, Martin K. ;
Farrand, Kathryn J. ;
Price, Kylie M. ;
Grasso, Carole ;
Miller, Rose J. ;
Hermans, Ian F. ;
McConnell, Melanie J. .
STEM CELLS, 2011, 29 (03) :452-461
[4]   Hematopoietic stem cells do not engraft with absolute efficiencies [J].
Camargo, FD ;
Chambers, SM ;
Drew, E ;
McNagny, KM ;
Goodell, MA .
BLOOD, 2006, 107 (02) :501-507
[5]   Distinct Hematopoietic Stem Cell Subtypes Are Differentially Regulated by TGF-β1 [J].
Challen, Grant A. ;
Boles, Nathan C. ;
Chambers, Stuart M. ;
Goodell, Margaret A. .
CELL STEM CELL, 2010, 6 (03) :265-278
[6]   How powerful is CD133 as a cancer stem cell marker in brain tumors? [J].
Cheng, Jin-Xiang ;
Liu, Bo-Lin ;
Zhang, Xiang .
CANCER TREATMENT REVIEWS, 2009, 35 (05) :403-408
[7]   The cancer stem cell: premises, promises and challenges [J].
Clevers, Hans .
NATURE MEDICINE, 2011, 17 (03) :313-319
[8]   CD133 is a temporary marker of cancer stem cells in small cell lung cancer, but not in non-small cell lung cancer [J].
Cui, Fei ;
Wang, Jian ;
Chen, Duan ;
Chen, Yi-Jiang .
ONCOLOGY REPORTS, 2011, 25 (03) :701-708
[9]   ABCG2: A potential marker of stem cells and novel target in stern cell and cancer therapy [J].
Ding, Xi-wei ;
Wu, Jun-hua ;
Jiang, Chun-ping .
LIFE SCIENCES, 2010, 86 (17-18) :631-637
[10]   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