## Abstract The detection of disseminated tumor cells in peripheral blood from colorectal cancer patients by RT‐PCR could be an attractive method for selecting patients for adjuvant therapy. We here report on real‐time RT‐PCR assays (LightCycler) to quantitate potential mRNA markers. We investigate
Detection of occult tumour cells in lymph nodes of colorectal cancer patients using real-time quantitative RT-PCR for CEA and CK20 mRNAS
✍ Scribed by Åke N.V. Öberg; Gudrun E. Lindmark; Anne C.E. Israelsson; Sten G. Hammarström; Marie-Louise K.C. Hammarström
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- French
- Weight
- 180 KB
- Volume
- 111
- Category
- Article
- ISSN
- 0020-7136
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✦ Synopsis
Abstract
The purpose of our study was to develop specific, sensitive, objective assays for early detection of disseminated tumour cells in patients with colorectal cancer (CRC). Carcinoembryonic antigen (CEA) and cytokeratin 20 (CK20) were chosen as markers because they are selectively expressed in epithelial cells with maintained expression in CRC. Real‐time quantitative RT‐PCR assays with RNA copy standards were constructed. Regional lymph nodes were collected from patients with CRC (n = 51) and benign intestinal disease (n = 10). Results were compared to routine histopathology and anti‐CEA immunohistochemistry. Lymph node levels of CEA and CK20 mRNA correlated strongly (p < 0.0001, r = 0.8). Lymph nodes from non‐CRC patients had <0.01 CEA and <0.001 CK20 mRNA copies/18S rRNA unit. Lymph nodes from 3/6 Dukes' A, 17/26 Dukes' B, 10/10 Dukes' C and 7/9 Dukes' D patients had CEA mRNA levels above cut‐off. Corresponding figures for CK20 mRNA were 3/6, 10/26, 9/10 and 5/9, respectively. CEA mRNA levels varied from 0.001 to 100 copies/18S rRNA unit in Dukes' A and B, and 50% of the Dukes' B patients had CEA mRNA levels within the range of Dukes' C patients. Three Dukes' B patients have died from CRC or developed distant metastases. All 3 had high CEA and CK20 mRNA levels. Determination of mRNA was superior to immunohistochemistry in showing CEA expression in lymph nodes. The present qRT‐PCR assay for CEA mRNA seems to be a superior tool to identify individuals with disseminated tumour cells. Future extended studies will establish the clinically most relevant cut‐off level. © 2004 Wiley‐Liss, Inc.
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