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Monitoring of circulating tumour-associated DNA as a prognostic tool for oral squamous cell carcinoma
Frequent allelic imbalances (AIs) including loss of heterozygosity and microsatellite instability on a specific chromosomal region have been identified in a variety of human malignancies. The objective of our study was to assess the possibility of prognostication and monitoring of oral squamous cell...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2005
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361808/ https://www.ncbi.nlm.nih.gov/pubmed/15928666 http://dx.doi.org/10.1038/sj.bjc.6602635 |
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author | Hamana, K Uzawa, K Ogawara, K Shiiba, M Bukawa, H Yokoe, H Tanzawa, H |
author_facet | Hamana, K Uzawa, K Ogawara, K Shiiba, M Bukawa, H Yokoe, H Tanzawa, H |
author_sort | Hamana, K |
collection | PubMed |
description | Frequent allelic imbalances (AIs) including loss of heterozygosity and microsatellite instability on a specific chromosomal region have been identified in a variety of human malignancies. The objective of our study was to assess the possibility of prognostication and monitoring of oral squamous cell carcinoma (SCC) by microsatellite blood assay. DNA from normal and tumorous tissues and serum DNA obtained at three time points (preoperatively, postoperatively, and 4 weeks postoperatively) from 64 patients with oral SCC was examined at nine microsatellite loci. In all, 38 (59%) DNA samples from tumorous tissues and 52% from serum showed AIs in at least one locus. Patterns of AIs in the serum DNA were matched to those detected in tumour DNA. Of them, AIs were frequently detected preoperatively (44%, 28 of 64), and postoperatively (20%, 13 of 64). Moreover, among 12 cases with AIs during the postoperative period, six had no evidence of an AI 4 weeks postoperatively, and they had no recurrence and were disease free. In contrast, six patients with AI-positive DNA 4 weeks postoperatively have died with distant metastasis within 44 weeks. Thus, our results suggest that the assessment of microsatellite status in the serum DNA could be a useful predictive tool to monitor disease prognosis. |
format | Text |
id | pubmed-2361808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23618082009-09-10 Monitoring of circulating tumour-associated DNA as a prognostic tool for oral squamous cell carcinoma Hamana, K Uzawa, K Ogawara, K Shiiba, M Bukawa, H Yokoe, H Tanzawa, H Br J Cancer Molecular Diagnostics Frequent allelic imbalances (AIs) including loss of heterozygosity and microsatellite instability on a specific chromosomal region have been identified in a variety of human malignancies. The objective of our study was to assess the possibility of prognostication and monitoring of oral squamous cell carcinoma (SCC) by microsatellite blood assay. DNA from normal and tumorous tissues and serum DNA obtained at three time points (preoperatively, postoperatively, and 4 weeks postoperatively) from 64 patients with oral SCC was examined at nine microsatellite loci. In all, 38 (59%) DNA samples from tumorous tissues and 52% from serum showed AIs in at least one locus. Patterns of AIs in the serum DNA were matched to those detected in tumour DNA. Of them, AIs were frequently detected preoperatively (44%, 28 of 64), and postoperatively (20%, 13 of 64). Moreover, among 12 cases with AIs during the postoperative period, six had no evidence of an AI 4 weeks postoperatively, and they had no recurrence and were disease free. In contrast, six patients with AI-positive DNA 4 weeks postoperatively have died with distant metastasis within 44 weeks. Thus, our results suggest that the assessment of microsatellite status in the serum DNA could be a useful predictive tool to monitor disease prognosis. Nature Publishing Group 2005-06-20 2005-05-31 /pmc/articles/PMC2361808/ /pubmed/15928666 http://dx.doi.org/10.1038/sj.bjc.6602635 Text en Copyright © 2005 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Molecular Diagnostics Hamana, K Uzawa, K Ogawara, K Shiiba, M Bukawa, H Yokoe, H Tanzawa, H Monitoring of circulating tumour-associated DNA as a prognostic tool for oral squamous cell carcinoma |
title | Monitoring of circulating tumour-associated DNA as a prognostic tool for oral squamous cell carcinoma |
title_full | Monitoring of circulating tumour-associated DNA as a prognostic tool for oral squamous cell carcinoma |
title_fullStr | Monitoring of circulating tumour-associated DNA as a prognostic tool for oral squamous cell carcinoma |
title_full_unstemmed | Monitoring of circulating tumour-associated DNA as a prognostic tool for oral squamous cell carcinoma |
title_short | Monitoring of circulating tumour-associated DNA as a prognostic tool for oral squamous cell carcinoma |
title_sort | monitoring of circulating tumour-associated dna as a prognostic tool for oral squamous cell carcinoma |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361808/ https://www.ncbi.nlm.nih.gov/pubmed/15928666 http://dx.doi.org/10.1038/sj.bjc.6602635 |
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