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Laboratory Investigation

Telomere Metabolism and Diagnostic Demonstration of Telomere Measurement in the Human Esophagus for Distinguishing Benign from Malignant Tissue by Tissue Quantitative Fluorescence in situ Hybridization

Kammori M.a-c · Izumiyama N.c · Nakamura K.c · Kurabayashi R.b, c · Kashio M.c, d · Aida J.c · Poon S.S.S.e · Kaminishi M.b

Author affiliations

aDepartment of Breast, Tokyo Metropolitan Tama Cancer Detection Center, bDivision of Gastrointestinal Surgery, and Metabolic Care and Endocrinological Surgery, Department of Surgery, Graduate School of Medicine, University of Tokyo, cResearch Team for Geriatric Disease, Tokyo Metropolitan Institute of Gerontology, and dDivision of Breast and Endocrine Surgery, Department of Surgery, Nihon University, Tokyo, Japan; eTerry Fox Laboratory, British Columbia Cancer Research Center, Vancouver, B.C., Canada

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Oncology 2006;71:430–436

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Article / Publication Details

First-Page Preview
Abstract of Laboratory Investigation

Received: June 01, 2007
Accepted: February 06, 2007
Published online: September 18, 2007
Issue release date: October 2007

Number of Print Pages: 7
Number of Figures: 3
Number of Tables: 0

ISSN: 0030-2414 (Print)
eISSN: 1423-0232 (Online)

For additional information: https://www.karger.com/OCL

Abstract

Objective: We have developed a novel method for evaluating telomere length in four different cell types in non-cancerous and cancerous mucosal tissue from 15 cases of squamous cell carcinoma of the esophagus using tissue quantitative fluorescence in situ hybridization (Q-FISH). We hypothesized that the very rapid cell proliferation observed in esophageal squamous cell carcinomas might accelerate the telomere shortening and chromosomal instability associated with carcinogenesis. Methods: Tissue Q-FISH and the telomere to centromere intensity ratio (TCR) were used to compare telomere shortening in tissue sections taken from esophageal squamous cell carcinomas and adjacent non-cancerous esophageal tissues. Results: The peak percentage of TCR was <1 for esophageal squamous carcinoma cells and >1 for the non-cancerous esophageal cell types. Basal layer cells had the longest telomeres in comparison with prickle, cancer, and stromal cells, and strongly expressed hTERT, cytokeratin 14 and CD49f, but not MIB-1. Conclusion: These results suggest the presence of stem cells in the basal layer of the esophagus. Esophageal squamous cell carcinomas also display anaphase bridges, evidencing chromosomal instability.In conclusion, our TCR method can be used to distinguish between benign and malignant tissue in esophageal lesions. In order to apply this approach clinically to individual cases, further studies are in progress.

© 2006 S. Karger AG, Basel


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    External Resources
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Article / Publication Details

First-Page Preview
Abstract of Laboratory Investigation

Received: June 01, 2007
Accepted: February 06, 2007
Published online: September 18, 2007
Issue release date: October 2007

Number of Print Pages: 7
Number of Figures: 3
Number of Tables: 0

ISSN: 0030-2414 (Print)
eISSN: 1423-0232 (Online)

For additional information: https://www.karger.com/OCL


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