mRNA expression profiles in circulating tumor cells of metastatic colorectal cancer patients

被引:50
作者
Mostert, Bianca [1 ]
Sieuwerts, Anieta M. [1 ,2 ]
Bolt-de Vries, Joan [1 ]
Kraan, Jaco [1 ]
Lalmahomed, Zarina [3 ]
van Galen, Anne [1 ]
van der Spoel, Petra [1 ]
de Weerd, Vanja [1 ]
Ramirez-Moreno, Raquel [1 ]
Smid, Marcel [1 ,2 ]
Verhoef, Cornelis [3 ]
IJzermans, Jan N. M. [3 ]
Gratama, Jan W. [1 ]
Sleijfer, Stefan [1 ,2 ]
Foekens, John A. [1 ]
Martens, John W. M. [1 ,2 ]
机构
[1] Erasmus Univ, Med Ctr, Erasmus MC Canc Inst, Dept Med Oncol, Rotterdam, Netherlands
[2] Erasmus Univ, Med Ctr, Erasmus MC Canc Inst, Canc Genom Netherlands, Rotterdam, Netherlands
[3] Erasmus Univ, Med Ctr, Dept Surg, Rotterdam, Netherlands
关键词
Circulating tumor cells; Metastatic colorectal cancer; Liver resection; Gene expression; Real-time PCR; ACID-BINDING PROTEIN; HEPATIC RESECTION; MICROSATELLITE INSTABILITY; PERIPHERAL-BLOOD; LIVER METASTASES; RECTAL-CANCER; SURVIVAL; BREAST; COLON; GENE;
D O I
10.1016/j.molonc.2015.01.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: The molecular characterization of circulating tumor cells (CTCs) is a promising tool for the repeated and non-invasive evaluation of predictive and prognostic factors. Challenges associated with CTC characterization using the only FDA approved method for CTC enumeration, the CellSearch technique, include the presence of an excess of leukocytes in CTC-enriched blood fractions. Here we aimed to identify colorectal tumor-specific gene expression levels in the blood of patients with and without detectable CTCs according to CellSearch criteria. Materials and methods: Blood of 30 healthy donors (HDs) and 142 metastatic colorectal cancer (mCRC) patients was subjected to CellSearch CTC enumeration and isolation. In all samples, 95 mRNAs were measured by reverse transcriptase quantitative PCR (RT-qPCR). HD blood samples and patient samples with three or more CTCs were compared to identify CTC-specific mRNAs. Patient samples without detectable CTCs were separately analyzed. Results: Thirty-four CTC-specific mRNAs were higher expressed in patients with >= 3 CTCs compared with HDs (Mann Whitney U-test P < 0.05). Among patients without detectable CTCs, a HD-unlike subgroup was identified which could be distinguished from HDs by the expression of epithelial genes such as KRT19, KRT20 and AGR2. Also, in an independent patient set, a similar HD-unlike group could be identified among the patients without detectable CTCs according to the CellSearch system. Conclusion: Extensive molecular characterization of colorectal CTCs is feasible and a subgroup of patients without detectable CTCs according to CellSearch criteria bears circulating tumor load, which may have clinical consequences. This CTC-specific gene panel for mCRC patients may enable the exploration of CTC characterization as a novel means to further individualize cancer treatment. (C) 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:920 / 932
页数:13
相关论文
共 60 条
[1]  
Abdalla EK, 2004, ANN SURG, V239, P818, DOI 10.1097/01.sla.0000128305.90650.71
[2]   Is hepatic resection justified after chemotherapy in patients with colorectal liver metastases and lymph node involvement? [J].
Adam, Rene ;
de Haas, Robbert J. ;
Wicherts, Dennis A. ;
Aloia, Thomas A. ;
Delvart, Valerie ;
Azoulay, Daniel ;
Bismuth, Henri ;
Castaing, Denis .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (22) :3672-3680
[3]   Circulating Tumor Cells: Liquid Biopsy of Cancer [J].
Alix-Panabieres, Catherine ;
Pantel, Klaus .
CLINICAL CHEMISTRY, 2013, 59 (01) :110-118
[4]   Circulating Tumor Cell Analysis: Technical and Statistical Considerations for Application to the Clinic [J].
Allan, Alison L. ;
Keeney, Andmichael .
JOURNAL OF ONCOLOGY, 2010, 2010
[5]   REG1A expression is a prognostic marker in colorectal cancer and associated with peritoneal carcinomatosis [J].
Astrosini, Christian ;
Roeefzaad, Claudia ;
Dai, Yi-Yang ;
Dieckgraefe, Brian K. ;
Joens, Thomas ;
Kemmner, Wolfgang .
INTERNATIONAL JOURNAL OF CANCER, 2008, 123 (02) :409-413
[6]   Characterization of ERG, AR and PTEN Gene Status in Circulating Tumor Cells from Patients with Castration-Resistant Prostate Cancer [J].
Attard, Gerhardt ;
Swermenhuis, Joost F. ;
Olmos, David ;
Reid, Alison H. M. ;
Vickers, Elaine ;
A'Hern, Roger ;
Levink, Rianne ;
Coumans, Frank ;
Moreira, Joana ;
Riisnaes, Ruth ;
Oommen, Nikhil Babu ;
Hawche, George ;
Jameson, Charles ;
Thompson, Emilda ;
Sipkema, Ronald ;
Carden, Craig P. ;
Parker, Christopher ;
Dearnaley, David ;
Kaye, Stan B. ;
Cooper, Colin S. ;
Molina, Arturo ;
Cox, Michael E. ;
Terstappen, Leon W. M. M. ;
de Bono, Johann S. .
CANCER RESEARCH, 2009, 69 (07) :2912-2918
[7]   Is the Clinical Risk Score for Patients with Colorectal Liver Metastases Still Useable in the Era of Effective Neoadjuvant Chemotherapy? [J].
Ayez, Ninos ;
Lalmahomed, Zarina S. ;
van der Pool, Anne E. M. ;
Vergouwe, Yvonne ;
van Montfort, Kees ;
de Jonge, Jeroen ;
Eggermont, Alexander M. M. ;
IJzermans, Jan N. M. ;
Verhoef, Cornelis .
ANNALS OF SURGICAL ONCOLOGY, 2011, 18 (10) :2757-2763
[8]   Prevalence and Heterogeneity of KRAS, BRAF, and PIK3CA Mutations in Primary Colorectal Adenocarcinomas and Their Corresponding Metastases [J].
Baldus, Stephan E. ;
Schaefer, Karl-L. ;
Engers, Rainer ;
Hartleb, Dinah ;
Stoecklein, Nikolas H. ;
Gabbert, Helmut E. .
CLINICAL CANCER RESEARCH, 2010, 16 (03) :790-799
[9]   LIVER-INTESTINE CADHERIN - MOLECULAR-CLONING AND CHARACTERIZATION OF A NOVEL CA2+-DEPENDENT CELL-ADHESION MOLECULE EXPRESSED IN LIVER AND INTESTINE [J].
BERNDORFF, D ;
GESSNER, R ;
KREFT, B ;
SCHNOY, N ;
LAJOUSPETTER, AM ;
LOCH, N ;
REUTTER, W ;
HORTSCH, M ;
TAUBER, R .
JOURNAL OF CELL BIOLOGY, 1994, 125 (06) :1353-1369
[10]   High Survival Rate After Two-Stage Resection of Advanced Colorectal Liver Metastases: Response-Based Selection and Complete Resection Define Outcome [J].
Brouquet, Antoine ;
Abdalla, Eddie K. ;
Kopetz, Scott ;
Garrett, Christopher R. ;
Overman, Michael J. ;
Eng, Cathy ;
Andreou, Andreas ;
Loyer, Evelyne M. ;
Madoff, David C. ;
Curley, Steven A. ;
Vauthey, Jean-Nicolas .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (08) :1083-1090