Stem-like features of cancer cells on their way to metastasis

被引:37
作者
Gkountela, Sofia [1 ]
Aceto, Nicola [1 ]
机构
[1] Univ Basel, Dept Biomed, Canc Metastasis, Mattenstr 28, CH-4058 Basel, Switzerland
基金
瑞士国家科学基金会; 欧洲研究理事会;
关键词
Cancer metastasis; Circulating tumor cells; CTCs; CTC clusters; Stem-like features; CIRCULATING TUMOR-CELLS; PERIPHERAL-BLOOD; SELF-RENEWAL; LABEL-FREE; EXPRESSION; CAPTURE; IDENTIFICATION; MARKER; DEVICE; HETEROGENEITY;
D O I
10.1186/s13062-016-0135-4
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
More than 90 % of cancer-related deaths are due to the development of a systemic metastatic disease. Clearly, much remains to be understood about the biological principles that govern human cancer metastasis, aiming at the ambitious objective to decrease metastasis-related mortality in patients. For many years, research on metastasis has been conducted in great part on experimental mouse models, mainly because of the difficulties in sampling, longitudinal studies, and molecular interrogation of a human metastatic disease. However, recently, extraordinary advances in microfluidic technologies are allowing the isolation and characterization of human circulating tumor cells (CTCs) that escaped a primary tumor mass and are in the process of seeding a distant metastasis. Analysis of human CTCs has now revealed important features of cancer metastasis, such as the high metastatic potential of CTC-clusters compared to single CTCs, the dynamic expression of epithelial and mesenchymal markers on CTCs during treatment, and the possibility to culture CTCs from patients for a real-time and individualized testing of drug susceptibility. Nevertheless, several aspects of CTC biology remain unsolved, such as the characterization of the stem-like cell population among human CTCs. Here, we focus on describing the latest findings in the CTC field, and discuss them in the context of cancer stem cell biology. Defining the molecular features of those few metastasis-initiating, stem-like CTCs holds the exceptional promise to develop metastasis-tailored therapies for patients with cancer.
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页数:14
相关论文
共 87 条
[1]   Circulating Tumor Cell Clusters Are Oligoclonal Precursors of Breast Cancer Metastasis [J].
Aceto, Nicola ;
Bardia, Aditya ;
Miyamoto, David T. ;
Donaldson, Maria C. ;
Wittner, Ben S. ;
Spencer, Joel A. ;
Yu, Min ;
Pely, Adam ;
Engstrom, Amanda ;
Zhu, Huili ;
Brannigan, Brian W. ;
Kapur, Ravi ;
Stott, Shannon L. ;
Shioda, Toshi ;
Ramaswamy, Sridhar ;
Ting, David T. ;
Lin, Charles P. ;
Toner, Mehmet ;
Haber, Daniel A. ;
Maheswaran, Shyamala .
CELL, 2014, 158 (05) :1110-1122
[2]   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
[3]   Circulating Tumor Cells: Liquid Biopsy of Cancer [J].
Alix-Panabieres, Catherine ;
Pantel, Klaus .
CLINICAL CHEMISTRY, 2013, 59 (01) :110-118
[4]   Genetic variegation of clonal architecture and propagating cells in leukaemia [J].
Anderson, Kristina ;
Lutz, Christoph ;
van Delft, Frederik W. ;
Bateman, Caroline M. ;
Guo, Yanping ;
Colman, Susan M. ;
Kempski, Helena ;
Moorman, Anthony V. ;
Titley, Ian ;
Swansbury, John ;
Kearney, Lyndal ;
Enver, Tariq ;
Greaves, Mel .
NATURE, 2011, 469 (7330) :356-+
[5]  
[Anonymous], 2007, BIOL CANC
[6]   Circulating tumor cell enumeration by the CellSearch system: The clinician's guide to breast cancer treatment? [J].
Beije, Nick ;
Jager, Agnes ;
Sleijfer, Stefan .
CANCER TREATMENT REVIEWS, 2015, 41 (02) :144-150
[7]  
Bergman RA, 1996, ATLAS MICROSCOPIC AN
[8]   Embryonic transcription factors in human breast cancer [J].
Briegel, Karoline J. .
IUBMB LIFE, 2006, 58 (03) :123-132
[9]   Leukemia inhibitory factor (LIF) withdrawal activates mTOR signaling pathway in mouse embryonic stem cells through the MEK/ERK/TSC2 pathway [J].
Cherepkova, M. Y. ;
Sineva, G. S. ;
Pospelov, V. A. .
CELL DEATH & DISEASE, 2016, 7 :e2050-e2050
[10]  
Clarke Michael F, 2006, Cancer Res, V66, P9339, DOI 10.1158/0008-5472.CAN-06-3126