Author/Authors :
Yadegarazari, Reza hamadan university of medical sciences - research center for molecular medicine - department of genetics and molecular medicine, ايران , Hassanzadeh, Taghi hamadan university of medical sciences - research center for molecular medicine, ايران , Majlesi, Amir hamadan university of medical sciences - beheshti hospital - Department of Gastrointestinal Diseases, ايران , Keshvari, Amir tehran university of medical sciences tums - imam khomeini hospital - department of general surgery, تهران, ايران , Monsef Esfahani, Alireza hamadan university of medical sciences - Department of Pathology, ايران , Tootoonchi, Amirsasan hamadan university of medical sciences - research center for molecular medicine, ايران , Shabab, Nooshin hamadan university of medical sciences - research center for molecular medicine - department of genetics and molecular medicine, ايران , Saidijam, Massoud hamadan university of medical sciences - research center for molecular medicine - department of genetics and molecular medicine, ايران
Abstract :
Background: Efficient screening for detection of colorectal cancer (CRC) at earlier stages reduces its mortality. The purpose of this study was to investigate expression of carcinoembryonic antigen (CEA) and human telomerase reverse transcriptase (hTERT) mRNA in peripheral blood of CRC patients and to present strategies for early detection screen test. Methods: Twenty seven patients in non-metastatic stage and 27 healthy individuals were studied. Expression of CEA, hTERT mRNA and 18srRNA (18s subunit of ribosomal RNA, as reference gene) were determined based on real-time RT-PCR on 3 μg of total RNA from blood in 3 separate vials (1 μg per vial). Results: Positive expression rate of CEA mRNA (78%) and hTERT mRNA (81%) were higher in patient group (P 0.001). These rates were meaningfully higher than the results of individual vials containing only 1 μg of total RNA. Difference between Ct values of markers with 18srRNA (ΔCt) was higher in healthy group than patient one. Therefore, a ΔCt cut-off value was determined for distinguishing between true- and false-positive results. Concurrent expression of both markers was found in 67% of the patients, which was higher than healthy cases (11%). Combination of concurrent marker expression with cut-off point strategy increased specificity to 100%. Conclusion: These results showed that concurrent evaluation of marker expression and performing the test on 3 μg of samples in 3 separate vials may increase specificity and sensitivity of real-time RT-PCR for early detection of non-metastatic CRC. However, more investigations with larger numbers of samples are needed to verify these results.
