Cancer stem cells - old concepts, new insights

被引:274
作者
Vermeulen, L. [1 ]
Sprick, M. R. [1 ]
Kemper, K. [1 ]
Stassi, G. [2 ]
Medema, J. P. [1 ]
机构
[1] Acad Med Ctr, LEXOR, Ctr Expt Mol Med, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Palermo, Dept Surg & Oncol Sci, Cellular & Mol Pathophysiol Lab, Palermo, Italy
关键词
cancer; cancer stem cell; tumor initiating cells; stem cells; differentiation; epigenetics;
D O I
10.1038/cdd.2008.20
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cancer has long been viewed as an exclusively genetic disorder. The model of carcinogenesis, postulated by Nowell and Vogelstein, describes the formation of a tumor by the sequential accumulation of mutations in oncogenes and tumor suppressor genes. In this model, tumors are thought to consist of a heterogeneous population of cells that continue to acquire new mutations, resulting in a highly dynamic process, with clones that out compete others due to increased proliferative or survival capacity. However, novel insights in cancer stem cell research suggest another layer of complexity in the process of malignant transformation and preservation. It has been reported that only a small fraction of the cancer cells in a malignancy have the capacity to propagate the tumor upon transplantation into immuno-compromised mice. Those cells are termed 'cancer stem cells' (CSC) and can be selected based on the expression of cell surface markers associated with immature cell types. In this review, we will critically discuss these novel insights in CSC-related research. Where possible we integrate these results within the genetic model of cancer and illustrate that the CSC model can be considered an extension of the classic genetic model rather than a contradictory theory. Finally, we discuss some of the most controversial issues in this field.
引用
收藏
页码:947 / 958
页数:12
相关论文
共 121 条
[1]  
Abraham BK, 2005, CLIN CANCER RES, V11, P1154
[2]   Therapeutic implications of cancer stem cells [J].
Al-Hajj, M ;
Becker, MW ;
Wichal, M ;
Weissman, I ;
Clarke, MF .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2004, 14 (01) :43-47
[3]   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
[4]   Most early disseminated cancer cells detected in bone marrow of breast cancer patients have a putative breast cancer stem cell phenotype [J].
Balic, Marija ;
Lin, Henry ;
Young, Lillian ;
Hawes, Debra ;
Giuliano, Armando ;
McNamara, George ;
Datar, Ram H. ;
Cote, Richard J. .
CLINICAL CANCER RESEARCH, 2006, 12 (19) :5615-5621
[5]   Glioma stem cells promote radioresistance by preferential activation of the DNA damage response [J].
Bao, Shideng ;
Wu, Qiulian ;
McLendon, Roger E. ;
Hao, Yueling ;
Shi, Qing ;
Hjelmeland, Anita B. ;
Dewhirst, Mark W. ;
Bigner, Darell D. ;
Rich, Jeremy N. .
NATURE, 2006, 444 (7120) :756-760
[6]   Oligodendrocyte-type-2 astrocyte (O-2A) progenitor cells transformed with c-myc and H-ras form high-grade glioma after stereotactic injection into the rat brain [J].
Barnett, SC ;
Robertson, L ;
Graham, D ;
Allan, D ;
Rampling, R .
CARCINOGENESIS, 1998, 19 (09) :1529-1537
[7]   Context, tissue plasticity, and cancer: Are tumor stem cells also regulated by the microenvironment? [J].
Bissell, MJ ;
LaBarge, MA .
CANCER CELL, 2005, 7 (01) :17-23
[8]   Turning brain into blood: A hematopoietic fate adopted by adult neural stem cells in vivo [J].
Bjornson, CRR ;
Rietze, RL ;
Reynolds, BA ;
Magli, MC ;
Vescovi, AL .
SCIENCE, 1999, 283 (5401) :534-537
[9]   Epithelial stem cells: Turning over new leaves [J].
Blanpain, Cedric ;
Horsley, Valerie ;
Fuchs, Elaine .
CELL, 2007, 128 (03) :445-458
[10]   The evolving concept of a stem cell: Entity or function? [J].
Blau, HM ;
Brazelton, TR ;
Weimann, JM .
CELL, 2001, 105 (07) :829-841