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Article type: Research Article
Authors: Molnar, Bela | Floro, Lajos | Sipos, Ferenc | Toth, Bernadett | Sreter, Lydia | Tulassay, Zsolt
Affiliations: II. Department of Medicine, Semmelweis University, 1088 Budapest, Hungary
Note: [] Corresponding author: Bela Molnar, M.D., Ph.D, II. Department of Medicine, Szentkirályi Str. 46, 1088 Budapest, Hungary. Tel.: +36 209 581499; Fax: +36 1 2660816; E-mail: mb@bel2.sote.hu
Abstract: Aims: Cytokeratin(CK) based real-time RT-PCR assays (QRT-PCR) are now available for peripheral blood circulating tumor cell (CTC) evaluations in colorectal cancer(CRC) patients. Results are non-existent for the application of these techniques to the determination of progression and therapy response in Dukes stage D CRC patients. Patients and methods: Each month 30~ml peripheral blood of 30 Dukes D patients (17 with progression) were drawn. CEA, CA19-9, CA72-A and TPA-M determinations were made. CK20, thymidilate synthase(TS) QRT-PCR was performed, as well. Buffy coat was used for immunmagnetic cancer cell isolation and CTC counting. Correlation between elevated CTC and macroscopic progression within 3 months was determined by Chi^{2} test. Results: Microscopic CTC single cell, doublet, cluster number were found in correlation with CK20 QRT-PCR results (p< 0.01). There was a significant increase in microscopic CTC number, CK20 and decrease in TS QRT-PCR levels (p< 0.05) in the peripheral blood of the non-responder as compared to responder patients. Elevation of the CTC was in significant correlation with macroscopic progression of the disease in 3 months (p< 0.01). Conclusions: CTC number reflects the chemotherapeutic sensitivity of CRC patients. Elevation of circulating tumor cell number in peripheral blood is in correlation with macroscopic progression.
Keywords: Circulating tumor cells, colorectal cancer, CK-20 RT-PCR, microscopic counting, progression
Journal: Disease Markers, vol. 24, no. 3, pp. 141-150, 2008
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