Mechanisms of Disease: cancer stem cells - targeting the evil twin

被引:150
作者
Trumpp, Andreas [1 ]
Wiestler, Otmar D. [2 ]
机构
[1] EPFL, Swiss Inst Expt Canc Res, Genet & Stem Cell Lab, Sch Life Sci, CH-1066 Epalinges, Switzerland
[2] German Canc Res Ctr, D-6900 Heidelberg, Germany
来源
NATURE CLINICAL PRACTICE ONCOLOGY | 2008年 / 5卷 / 06期
关键词
cancer-initiating cell; chemotherapy; multidrug resistance; self-renewal; stem-cell niche;
D O I
10.1038/ncponc1110
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Classical antineoplastic treatments such as chemotherapy or radiation can efficiently eradicate the majority of proliferating and genetically unstable malignant cells within neoplastic lesions. There is increasing evidence, however, that these regimens frequently fail to eliminate a minor subpopulation of resistant tumor cells that have distinct features of somatic stem cells. These serve as a reservoir for disease recurrence, and are the origin of metastatic growth. These so-called cancer stem cells (CSCs) or cancer-initiating cells represent often a rare, highly self-renewing population within the tumor mass, which is thought to be the only one required for both initiation and maintenance of disease. Tumor-cell populations enriched for CSC activity were originally identified in leukemias, but have now also been uncovered in a number of solid cancers. Their marked resistance towards classical antitumor regimens is mediated by the combination of several critical features, including relative dormancy, efficient DNA repair, high expression of multidrug-resistance-type membrane transporters and protection by a hypoxic niche environment. We review the concept of CSCs with particular emphasis on the mechanism of therapy resistance, and discuss potential future therapeutic interventions with the goal of specifically eliminating CSCs in a clinical setting.
引用
收藏
页码:337 / 347
页数:11
相关论文
共 100 条
[1]  
Abraham BK, 2005, CLIN CANCER RES, V11, P1154
[2]   Models, mechanisms and clinical evidence for cancer dormancy [J].
Aguirre-Ghiso, Julio A. .
NATURE REVIEWS CANCER, 2007, 7 (11) :834-846
[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]   Tissue repair and stem cell renewal in carcinogenesis [J].
Beachy, PA ;
Karhadkar, SS ;
Berman, DM .
NATURE, 2004, 432 (7015) :324-331
[6]   Persistence of malignant hematopoietic progenitors in chronic myelogenous leukemia patients in complete cytogenetic remission following imatinib mesylate treatment [J].
Bhatia, R ;
Holtz, M ;
Niu, N ;
Gray, R ;
Snyder, DS ;
Sawyers, CL ;
Arber, DA ;
Slovak, ML ;
Forman, SJ .
BLOOD, 2003, 101 (12) :4701-4707
[7]  
BIEDLER JL, 1970, CANCER RES, V30, P1174
[8]   Primitive acute myeloid leukemia cells with long-term proliferative ability in vitro and in vivo lack surface expression of c-kit (CD 117) [J].
Blair, A ;
Sutherland, HJ .
EXPERIMENTAL HEMATOLOGY, 2000, 28 (06) :660-671
[9]   Epithelial stem cells: Turning over new leaves [J].
Blanpain, Cedric ;
Horsley, Valerie ;
Fuchs, Elaine .
CELL, 2007, 128 (03) :445-458
[10]   Human acute myeloid leukemia is organized as a hierarchy that originates from a primitive hematopoietic cell [J].
Bonnet, D ;
Dick, JE .
NATURE MEDICINE, 1997, 3 (07) :730-737