Detection of colorectal cancer cells in peripheral blood by reverse-transcriptase polymerase chain reaction for cytokeratin 20

被引:0
|
作者
Wyld, DK
Selby, P
Perren, TJ
Jonas, SK
Allen-Mersh, TG
Wheeldon, J
Burchill, SA
机构
[1] St James Univ Hosp, ICRF Canc Med Res Unit, Leeds LS9 7TF, W Yorkshire, England
[2] St James Univ Hosp, Candlelighters Childrens Canc Res Lab, Leeds LS9 7TF, W Yorkshire, England
[3] Chelsea & Westminster Hosp, Imperial Coll Sch Med, Dept Surg, London, England
关键词
D O I
10.1002/(SICI)1097-0215(19980619)79:3<288::AID-IJC14>3.3.CO;2-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The staging of colorectal cancer currently depends an pathological examination of the surgical specimen and regional lymph nodes, accompanied by imaging tests such as computed tomography (CT) scanning. However, alternative molecular methods to detect circulating tumour cells in blood or bone marrow may provide additional information about the extent of disease and prognosis. We have previously reported the development of a reverse-transcriptase polymerase chain reaction (RT-PCR) for cytokeratin 20 (CK 20) mRNA to detect circulating epithelial tumour cells. In this study, we report on the application of this method for detecting circulating tumour cells in patients with colorectal cancer. Using this method, CK 20 mRNA was detected in 8/8 human colorectal cancer cell lines, in 8/9 biopsies from primary colorectal rumours and in 9/10 biopsies of liver metastasis in patients with metastatic colorectal cancer, suggesting that CK 20 may be a useful target for the detection of circulating tumour cells in this patient group. in spiking experiments, 10 cells were consistently identified in 2 ml of whale blood (1 x 10(6)-1 x 10(7) mononuclear cells). In 12/25 (48%) peripheral blood samples from patients with known metastatic colorectal cancer, CK 20 mRNA was detected. However, there was no correlation between the detection of CK 20 mRNA in the peripheral blood and disease progression and survival in this group Of patients. CK 20 mRNA was detected in 1/12 normal blood samples, which raises questions about the absolute specificity of CM 20 expression. (C) 1998 Wiley-Liss, Inc.
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页码:288 / 293
页数:6
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