Detection of disseminated tumor cells in peripheral blood

被引:244
作者
Zieglschmid, V [1 ]
Hollmann, C [1 ]
Böcher, O [1 ]
机构
[1] AdnaGen AG, D-30853 Hannover, Germany
关键词
cancer; clinical significance; epithelial cancer cells; gene expression; immunomagnetic selection; multiple tumorr markers;
D O I
10.1080/10408360590913696
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
Metastases are the major cause of cancer-related deaths in patients with solid epithelial malignancies, such as breast, colorectal, and prostate carcinomas. Hematogenous spreading of tumor cells from a primary tumor can be considered as a crucial step ill the metastasis cascade leading eventually to the formation of clinically manifest metastases. Consequently, as shown in recent studies, the detection of disseminated tumor cells in peripheral blood might be of clinical relevance with respect to individual patient prognosis and staging or monitoring of therapy. However, the rarity of disseminated tumor cells in peripheral blood renders the application of sensitive techniques mandatory for their detection. The emergence of highly sophisticated reverse transcriptase-polymerase chain reaction (RT-PCR) assays, combining a preanalytical enrichment step with the assessment of multiple molecular tumor markers expressed in disseminated tumor cells, provides a powerful tool in detecting disseminated tumor cells with high sensitivity and specificity. This review will discuss currently used tumor markers as well as experimental means to enhance the sensitivity and specificity of RT-PCR assays to detect disseminated tumor cells in the peripheral blood of patients with breast, colorectal, and prostate cancers, and their clinical relevance assessed in recent studies.
引用
收藏
页码:155 / 196
页数:42
相关论文
共 220 条
[91]  
2-R
[92]  
Jarrard JA, 1998, CANCER RES, V58, P5582
[93]   Molecular detection of micro-metastasis in breast cancer [J].
Jiang, WG ;
Martin, TA ;
Mansel, RE .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2002, 43 (01) :13-31
[94]   Detection of micrometastasis by cytokeratin 20 RT-PCR is limited due to stable background transcription in granulocytes [J].
Jung, R ;
Petersen, K ;
Krüger, W ;
Wolf, M ;
Wagener, C ;
Zander, A ;
Neumaier, M .
BRITISH JOURNAL OF CANCER, 1999, 81 (05) :870-873
[95]   Specificity of reverse transcriptase polymerase chain reaction assays designed for the detection of circulating cancer cells is influenced by cytokines in vivo and in vitro [J].
Jung, R ;
Krüger, W ;
Hosch, S ;
Holweg, M ;
Kröger, N ;
Gutensohn, K ;
Wagener, C ;
Neumaier, M ;
Zander, AR .
BRITISH JOURNAL OF CANCER, 1998, 78 (09) :1194-1198
[96]   RT-PCR amplification of CK19 mRNA in the blood of breast cancer patients: correlation with established prognostic parameters [J].
Kahn, HJ ;
Yang, LY ;
Blondal, J ;
Lickley, L ;
Holloway, C ;
Hanna, W ;
Narod, S ;
McCready, DR ;
Seth, A ;
Marks, A ;
Marks, A .
BREAST CANCER RESEARCH AND TREATMENT, 2000, 60 (02) :143-151
[97]   Prognostic significance of reverse transcriptase polymerase chain reaction for prostate-specific antigen in men with hormone-refractory prostate cancer [J].
Kantoff, PW ;
Halabi, S ;
Farmer, DA ;
Hayes, DF ;
Vogelzang, NA ;
Small, EJ .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (12) :3025-3028
[98]  
Kantor A.B., 1998, CELL SEP METHODS APP, V1, P153
[99]   Haematogenous cytokeratin 20 mRNA as a predictive marker for recurrence in oral cancer patients [J].
Kawamata, H ;
Uchida, D ;
Nakashiro, K ;
Hino, S ;
Omotehara, F ;
Yoshida, H ;
Sato, R .
BRITISH JOURNAL OF CANCER, 1999, 80 (3-4) :448-452
[100]   Use of magnetic enrichment for detection of carcinoma cells in fluid specimens [J].
Kielhorn, E ;
Schofield, K ;
Rimm, DL .
CANCER, 2002, 94 (01) :205-211