Circulating Tumor Cells: Liquid Biopsy of Cancer

被引:871
作者
Alix-Panabieres, Catherine [1 ,2 ,3 ]
Pantel, Klaus [4 ]
机构
[1] St Eloi Hosp, Univ Med Ctr, Inst Res Biotherapy, Lab Rare Human Circulating Cells, Montpellier, France
[2] Arnaud de Villeneuve Hosp, Lab Cell & Hormonal Biol, Univ Med Ctr, Montpellier, France
[3] Univ Inst Clin Res UM1 EA2415 Epidemiol Biostat &, Montpellier, France
[4] Univ Med Ctr Hamburg Eppendorf, Dept Tumor Biol, Ctr Med Expt, Univ Canc Ctr Hamburg, D-20246 Hamburg, Germany
关键词
BREAST-CANCER; MOLECULAR CHARACTERIZATION; PERIPHERAL-BLOOD; PROGRESSION; EXPRESSION; DISEASE; EMT;
D O I
10.1373/clinchem.2012.194258
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
BACKGROUND: The detection and molecular characterization of circulating tumor cells (CTCs) are one of the most active areas of translational cancer research, with >400 clinical studies having included CTCs as a biomarker. The aims of research on CTCs include (a) estimation of the risk for metastatic relapse or metastatic progression (prognostic information), (b) stratification and real-time monitoring of therapies, (c) identification of therapeutic targets and resistance mechanisms, and (d) understanding metastasis development in cancer patients. CONTENT: This review focuses on the technologies used for the enrichment and detection of CTCs. We outline and discuss the current technologies that are based on exploiting the physical and biological properties of CTCs. A number of innovative technologies to improve methods for CTC detection have recently been developed, including CTC microchips, filtration devices, quantitative reverse-transcription PCR assays, and automated microscopy systems. Molecular-characterization studies have indicated, however, that CTCs are very heterogeneous, a finding that underscores the need for multiplex approaches to capture all of the relevant CTC subsets. We therefore emphasize the current challenges of increasing the yield and detection of CTCs that have undergone an epithelial mesenchymal transition. Increasing assay analytical sensitivity may lead, however, to a decrease in analytical specificity (e.g., through the detection of circulating normal epithelial cells). SUMMARY: A considerable number of promising CTC-detection techniques have been developed in recent years. The analytical specificity and clinical utility of these methods must be demonstrated in large prospective multicenter studies to reach the high level of evidence required for their introduction into clinical practice. (C) 2012 American Association for Clinical Chemistry
引用
收藏
页码:110 / 118
页数:9
相关论文
共 45 条
[1]  
Agrawal B, 1998, CANCER RES, V58, P4079
[2]   Detection and characterization of putative metastatic precursor cells in cancer patients [J].
Alix-Panabieres, Catherine ;
Vendrell, Jean-Pierre ;
Pelle, Olivier ;
Rebillard, Xavier ;
Riethdorf, Sabine ;
Mueller, Volkmar ;
Fabbro, Michel ;
Pantel, Klaus .
CLINICAL CHEMISTRY, 2007, 53 (03) :537-539
[3]  
Alix-Panabieres Catherine, 2012, Recent Results Cancer Res, V195, P69, DOI 10.1007/978-3-642-28160-0_6
[4]   Circulating Tumor Cells and Circulating Tumor DNA [J].
Alix-Panabieres, Catherine ;
Schwarzenbach, Heidi ;
Pantel, Klaus .
ANNUAL REVIEW OF MEDICINE, VOL 63, 2012, 63 :199-215
[5]   Full-length cytokeratin-19 is released by human tumor cells: a potential role in metastatic progression of breast cancer [J].
Alix-Panabieres, Catherine ;
Vendrell, Jean-Pierre ;
Slijper, Monique ;
Pelle, Olivier ;
Barbotte, Eric ;
Mercier, Gregoire ;
Jacot, William ;
Fabbro, Michel ;
Pantel, Klaus .
BREAST CANCER RESEARCH, 2009, 11 (03)
[6]   Comparison of assay methods for detection of circulating tumor cells in metastatic breast cancer: AdnaGen AdnaTest BreastCancer Select/Detect™ versus Veridex CellSearch™ system [J].
Andreopoulou, E. ;
Yang, L. -Y. ;
Rangel, K. M. ;
Reuben, J. M. ;
Hsu, L. ;
Krishnamurthy, S. ;
Valero, V. ;
Fritsche, H. A. ;
Cristofanilli, M. .
INTERNATIONAL JOURNAL OF CANCER, 2012, 130 (07) :1590-1597
[7]   BRCA1 Loss Preexisting in Small Subpopulations of Prostate Cancer Is Associated with Advanced Disease and Metastatic Spread to Lymph Nodes and Peripheral Blood [J].
Bednarz, Natalia ;
Eltze, Elke ;
Semjonow, Axel ;
Rink, Michael ;
Andreas, Antje ;
Mulder, Lennart ;
Hannemann, Juliane ;
Fisch, Margit ;
Pantel, Klaus ;
Weier, Heinz-Ulrich G. ;
Bielawski, Krzysztof P. ;
Brandt, Burkhard .
CLINICAL CANCER RESEARCH, 2010, 16 (13) :3340-3348
[8]   Plasticity of disseminating cancer cells in patients with epithelial malignancies [J].
Bednarz-Knoll, Natalia ;
Alix-Panabieres, Catherine ;
Pantel, Klaus .
CANCER AND METASTASIS REVIEWS, 2012, 31 (3-4) :673-687
[9]   A pooled analysis of bone marrow micrometastasis in breast cancer [J].
Braun, S ;
Vogl, FD ;
Naume, B ;
Janni, W ;
Osborne, MP ;
Coombes, RC ;
Schlimok, G ;
Diel, IJ ;
Gerber, B ;
Gebauer, G ;
Pierga, JY ;
Marth, C ;
Oruzio, D ;
Wiedswang, G ;
Solomayer, EF ;
Kundt, G ;
Strobl, B ;
Fehm, T ;
Wong, GYC ;
Bliss, J ;
Vincent-Salomon, A ;
Pantel, K .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (08) :793-802
[10]   Circulating tumor cells, disease progression, and survival in metastatic breast cancer [J].
Cristofanilli, M ;
Budd, GT ;
Ellis, MJ ;
Stopeck, A ;
Matera, J ;
Miller, MC ;
Reuben, JM ;
Doyle, GV ;
Allard, WJ ;
Terstappen, LWMM ;
Hayes, DF .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (08) :781-791