Real-Time qPCR-Based Detection of Circulating Tumor Cells from Blood Samples of Adjuvant Breast Cancer Patients: A Preliminary Study

被引:8
作者
Andergassen, Ulrich [1 ]
Zebisch, Michael [1 ]
Koelbl, Alexandra C. [1 ]
Koenig, Alexander [1 ]
Heublein, Sabine [1 ]
Schroeder, Lennard [1 ]
Hutter, Stefan [1 ]
Friese, Klaus [1 ]
Jeschke, Udo [1 ]
机构
[1] Univ Munich, Dept Obstet & Gynecol, Maistr 11, D-80337 Munich, Germany
关键词
Circulating tumor cells; RT-qPCR; Cytokeratins; Adjuvant breast cancer; RNA-POSITIVE CELLS; EPITHELIAL-CELLS; MESSENGER-RNA; PERIPHERAL-BLOOD; BONE-MARROW; PCR ASSAY; EXPRESSION; CYTOKERATIN-19; QUANTIFICATION; PROGRESSION;
D O I
10.1159/000447041
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Circulating tumor cells (CTCs) are cells that detach from a primary tumor, circulate through the blood stream and lymphatic vessels, and are considered to be the main reason for remote metastasis. Due to their origin, tumor cells have different gene expression levels than the surrounding blood cells. Therefore, they might be detectable in blood samples from breast cancer patients by real-time quantitative polymerase chain reaction (RT-qPCR). Materials and Methods: Blood samples of healthy donors and adjuvant breast cancer patients were withdrawn and the cell fraction containing white blood cells and tumor cells was enriched by density gradient centrifugation. RNA was isolated and reverse transcribed to cDNA, which was then used in TaqMan real-time PCR against cytokeratin (CK)8, CK18 and CK19. 18S and GAPDH were used as controls. Results: All 3 CKs were, on average, found to be significantly higher expressed in adjuvant breast cancer samples compared to negative controls, probably due to the presence of CTCs. Unfortunately, gene expression levels could not be correlated to tumor characteristics. Conclusions: RT-qPCR could make up a new approach for the detection of CTCs from blood samples of breast cancer patients, but a correlation of the PCR data to gold standard methods in CTC detection would help to further improve the informative value of the qPCR results. (C) 2016 S. Karger GmbH, Freiburg
引用
收藏
页码:194 / 198
页数:5
相关论文
共 42 条
  • [1] Tumor cells circulate in the peripheral blood of all major carcinomas but not in healthy subjects or patients with nonmalignant diseases
    Allard, WJ
    Matera, J
    Miller, MC
    Repollet, M
    Connelly, MC
    Rao, C
    Tibbe, AGJ
    Uhr, JW
    Terstappen, LWMM
    [J]. CLINICAL CANCER RESEARCH, 2004, 10 (20) : 6897 - 6904
  • [2] Andergassen Ulrich, 2013, Cancers (Basel), V5, P1212, DOI 10.3390/cancers5041212
  • [3] Detection of Tumor Cell-Specific mRNA in the Peripheral Blood of Patients with Breast Cancer-Evaluation of Several Markers with Real-Time Reverse Transcription-PCR
    Andergassen, Ulrich
    Hofmann, Simone
    Koelbl, Alexandra C.
    Schindlbeck, Christian
    Neugebauer, Julia
    Hutter, Stefan
    Engelstaedter, Verena
    Ilmer, Matthias
    Friese, Klaus
    Jeschke, Udo
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2013, 14 (01): : 1093 - 1104
  • [4] Clinical relevance of circulating CK-19mRNA-positive tumour cells before front-line treatment in patients with metastatic breast cancer
    Androulakis, N.
    Agelaki, S.
    Perraki, M.
    Apostolaki, S.
    Bozionelou, V.
    Pallis, A.
    Kalbakis, K.
    Xyrafas, A.
    Mavroudis, D.
    Georgoulias, V.
    [J]. BRITISH JOURNAL OF CANCER, 2012, 106 (12) : 1917 - 1925
  • [5] Axillary sentinel lymph nodes can be falsely positive due to iatrogenic displacement and transport of benign epithelial cells in patients with breast carcinoma
    Bleiweiss, IJ
    Nagi, CS
    Jaffer, S
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (13) : 2013 - 2018
  • [6] Cytokeratin-positive cells in the bone marrow and survival of patients with stage I, II, or III breast cancer.
    Braun, S
    Pantel, K
    Muller, P
    Janni, W
    Hepp, F
    Kentenich, CRM
    Gastroph, S
    Wischnik, A
    Dimpfl, T
    Kindermann, G
    Riethmuller, G
    Schlimok, G
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (08) : 525 - 533
  • [7] A pooled analysis of bone marrow micrometastasis in breast cancer
    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
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (08) : 793 - 802
  • [8] MMP13 is potentially a new tumor marker for breast cancer diagnosis
    Chang, Hui-Jen
    Yang, Ming-Je
    Yang, Yu-Hsiang
    Hou, Ming-Feng
    Hsueh, Er-Jung
    Lin, Shiu-Ru
    [J]. ONCOLOGY REPORTS, 2009, 22 (05) : 1119 - 1127
  • [9] Circulating tumor cells, disease progression, and survival in metastatic breast cancer
    Cristofanilli, M
    Budd, GT
    Ellis, MJ
    Stopeck, A
    Matera, J
    Miller, MC
    Reuben, JM
    Doyle, GV
    Allard, WJ
    Terstappen, LWMM
    Hayes, DF
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (08) : 781 - 791
  • [10] Detection of cytokeratin-19 mRNA-positive cells in the peripheral blood and bone marrow of patients with operable breast cancer
    Daskalaki, A.
    Agelaki, S.
    Perraki, M.
    Apostolaki, S.
    Xenidis, N.
    Stathopoulos, E.
    Kontopodis, E.
    Hatzidaki, D.
    Mavroudis, D.
    Georgoulias, V.
    [J]. BRITISH JOURNAL OF CANCER, 2009, 101 (04) : 589 - 597