Tackling the cancer stem cells - what challenges do they pose?

被引:903
作者
Pattabiraman, Diwakar R. [1 ]
Weinberg, Robert A. [1 ,2 ,3 ]
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02142 USA
[3] MIT, Ludwig Ctr Mol Oncol, Cambridge, MA 02139 USA
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; ACUTE MYELOID-LEUKEMIA; TUMOR-ASSOCIATED MACROPHAGES; ALDEHYDE DEHYDROGENASE 1; SIDE POPULATION CELLS; GROWTH-FACTOR-BETA; KINASE-C-ALPHA; TGF-BETA; ENDOTHELIAL-CELLS; PROGENITOR CELLS;
D O I
10.1038/nrd4253
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Since their identification in 1994, cancer stem cells (CSCs) have been objects of intensive study. Their properties and mechanisms of formation have become a major focus of current cancer research, in part because of their enhanced ability to initiate and drive tumour growth and their intrinsic resistance to conventional therapeutics. The discovery that activation of the epithelial-to-mesenchymal transition (EMT) programme in carcinoma cells can give rise to cells with stem-like properties has provided one possible mechanism explaining how CSCs arise and presents a possible avenue for their therapeutic manipulation. Here we address recent developments in CSC research, focusing on carcinomas that are able to undergo EMT. We discuss the signalling pathways that create these cells, cell-intrinsic mechanisms that could be exploited for selective elimination or induction of their differentiation, and the role of the tumour microenvironment in sustaining them. Finally, we propose ways to use our current knowledge of the complex biology of CSCs to design novel therapies to eliminate them.
引用
收藏
页码:497 / 512
页数:16
相关论文
共 255 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]
WNT signalling pathways as therapeutic targets in cancer [J].
Anastas, Jamie N. ;
Moon, Randall T. .
NATURE REVIEWS CANCER, 2013, 13 (01) :11-26
[4]
PRECURSORS OF COLONY-FORMING CELLS IN HUMANS CAN BE DISTINGUISHED FROM COLONY-FORMING CELLS BY EXPRESSION OF THE CD33 AND CD34 ANTIGENS AND LIGHT SCATTER PROPERTIES [J].
ANDREWS, RG ;
SINGER, JW ;
BERNSTEIN, ID .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 169 (05) :1721-1731
[5]
The ins and Outs of the Epithelial to Mesenchymal Transition in Health and Disease [J].
Angela Nieto, M. .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 27, 2011, 27 :347-376
[6]
TGF-β Receptor Inhibitors Target the CD44high/Id1high Glioma-Initiating Cell Population in Human Glioblastoma [J].
Anido, Judit ;
Saez-Borderias, Andrea ;
Gonzalez-Junca, Alba ;
Rodon, Laura ;
Folch, Gerard ;
Carmona, Maria A. ;
Prieto-Sanchez, Rosa M. ;
Barba, Ignasi ;
Martinez-Saez, Elena ;
Prudkin, Ludmila ;
Cuartas, Isabel ;
Raventos, Carolina ;
Martinez-Ricarte, Francisco ;
Antonia Poca, M. ;
Garcia-Dorado, David ;
Lahn, Michael M. ;
Yingling, Jonathan M. ;
Rodon, Jordi ;
Sahuquillo, Juan ;
Baselga, Jose ;
Seoane, Joan .
CANCER CELL, 2010, 18 (06) :655-668
[7]
Slow proliferation as a biological feature of colorectal cancer metastasis [J].
Anjomshoaa, A. ;
Nasri, S. ;
Humar, B. ;
McCall, J. L. ;
Chatterjee, A. ;
Yoon, H-S ;
McNoe, L. ;
Black, M. A. ;
Reeve, A. E. .
BRITISH JOURNAL OF CANCER, 2009, 101 (05) :822-828
[8]
POLAR APOLAR COMPOUNDS INDUCE LEUKEMIA-CELL DIFFERENTIATION BY MODULATING CELL-SURFACE POTENTIAL [J].
ARCANGELI, A ;
CARLA, M ;
DELBENE, MR ;
BECCHETTI, A ;
WANKE, E ;
OLIVOTTO, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (12) :5858-5862
[9]
Avalos AM, 2002, BIOL RES, V35, P231
[10]
Phosphatidylinositol 3-kinase function is required for transforming growth factor β-mediated epithelial to mesenchymal transition and cell migration [J].
Bakin, AV ;
Tomlinson, AK ;
Bhowmick, NA ;
Moses, HL ;
Arteaga, CL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (47) :36803-36810