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Quantitative Assessment of hTERT mRNA Expression in Dysplastic Nodules of HBV-Related Hepatocarcinogenesis

Oh, Bong-Kyeong, Ph.D.1,*; Kim, Young-Joo, M.S.1,*; Park, Young Nyun, M.D., Ph.D.1,3; Choi, Jinsub, M.D.2; Kim, Kyung Sik, M.D., Ph.D.2; Park, Chanil, M.D., Ph.D.1,3

American Journal of Gastroenterology: April 2006 - Volume 101 - Issue 4 - p 831–838
ORIGINAL CONTRIBUTION: PATHOLOGY
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BACKGROUND Telomerase reverse transcriptase (hTERT) is the rate-limiting determinant of telomerase, which is critical for carcinogenesis. Dysplastic nodules (DNs) appear to be preneoplastic lesions of hepatocellular carcinomas (HCCs). In this study, in order to characterize DNs, hTERT mRNA, hTERT gene dosage, and mRNA for c-myc, a transcriptional activator of hTERT were studied in human multi-step hepatocarcinogenesis.

METHODS Fifty four hepatic nodules including 5 large regenerative nodules, 14 low-grade DNs, 7 high-grade DNs, 11 DNs with HCC foci and 17 HCCs, 23 livers with chronic hepatitis/cirrhosis, and 6 normal livers were examined. Transcript levels were measured by real-time quantitative RT-PCR and gene dosages by real-time PCR and Southern blotting.

RESULTS The hTERT mRNA levels increased with the progression of hepatocarcinogenesis, and a significant induction in the transition between low- and high-grade DNs was seen. Most high-grade DNs strongly expressed hTERT mRNA at levels similar to those of HCCs. Twenty-one percent of low-grade DNs had high levels of hTERT mRNA, up to those of high-grade DNs and there was no difference in the pathological features between low-grade DNs with and without increased hTERT mRNA levels. No correlation was found between hTERT mRNA levels, hTERT gene dosage, and c-myc mRNA levels.

CONCLUSIONS These results suggest that the induction of hTERT mRNA is an important early event and that its measurement by real-time quantitative RT-PCR is a useful tool to detect premalignant/malignant tendencies in hepatic nodules. However, hTERT gene dosage and c-myc expression are not the main mechanisms regulating hTERT expression in hepatocarcinogenesis.

1Department of Pathology, Center for Chronic Metabolic Disease Research and Yonsei Biomedical Science and Technology Initiative, Yonsei University College of Medicine, Seoul, Korea

2Department of General Surgery, Yonsei University College of Medicine, Seoul, Korea

3Institute of Gastroenterology and Cell Homeostasis Care Centre, Yonsei University College of Medicine, Seoul, Korea

Reprint requests and correspondence: Young Nyun Park, M.D., Ph.D., Department of Pathology, and Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, CPO Box 8044, Seoul, Korea.

*These authors contributed equally to this work.

Received July 26, 2005; accepted October 19, 2005.

© The American College of Gastroenterology 2006. All Rights Reserved.
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