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The Clinicopathological Correlations of hTERC Amplification with Esophageal Squamous Cell Precursor Lesions
BACKGROUND: Esophageal squamous cell precursor lesions remain one of the most controversial topics in pathology and clinical management. AIMS: To analyze the dysregulation of human telomerase RNA component (hTERC) in esophageal squamous cell precursor lesions and the clinicopathological correlations...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318245/ https://www.ncbi.nlm.nih.gov/pubmed/30311151 http://dx.doi.org/10.1007/s10620-018-5318-7 |
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author | Hu, Yanping Teng, Xiaojing Wu, Linlin Liu, Wei An, Jianduo |
author_facet | Hu, Yanping Teng, Xiaojing Wu, Linlin Liu, Wei An, Jianduo |
author_sort | Hu, Yanping |
collection | PubMed |
description | BACKGROUND: Esophageal squamous cell precursor lesions remain one of the most controversial topics in pathology and clinical management. AIMS: To analyze the dysregulation of human telomerase RNA component (hTERC) in esophageal squamous cell precursor lesions and the clinicopathological correlations with the characteristics of esophageal squamous cell precursor lesions. METHODS: Florescence in situ hybridization was performed to detect hTERC amplification in different gradings of esophageal squamous cell precursor lesions. With retrospective follow-up data, clinicopathological correlations between hTERC and esophageal squamous cell precursor lesions were subjected to logistic regression analysis. RESULTS: hTERC amplification gradually increased with upgrading of dysplasia, reaching the highest level in high-grade intraepithelial neoplasia, and there was a significant difference between the low-grade intraepithelial neoplasia group and the high-grade intraepithelial neoplasia group (P = 0.00). Logistic regression analysis showed that hTERC amplification was correlated with both dysplasia grading and ulcer characteristics of esophageal squamous cell precursor lesions (P < 0.05). CONCLUSIONS: hTERC amplification with increasing grading of esophageal squamous cell precursor lesions and the presence of ulcer characteristics might provide an important molecular and pathological marker for the diagnosis and clinical prognosis of esophageal squamous cell precursor lesions, especially for those ambiguous cases with more divergence in classification. |
format | Online Article Text |
id | pubmed-6318245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-63182452019-01-14 The Clinicopathological Correlations of hTERC Amplification with Esophageal Squamous Cell Precursor Lesions Hu, Yanping Teng, Xiaojing Wu, Linlin Liu, Wei An, Jianduo Dig Dis Sci Original Article BACKGROUND: Esophageal squamous cell precursor lesions remain one of the most controversial topics in pathology and clinical management. AIMS: To analyze the dysregulation of human telomerase RNA component (hTERC) in esophageal squamous cell precursor lesions and the clinicopathological correlations with the characteristics of esophageal squamous cell precursor lesions. METHODS: Florescence in situ hybridization was performed to detect hTERC amplification in different gradings of esophageal squamous cell precursor lesions. With retrospective follow-up data, clinicopathological correlations between hTERC and esophageal squamous cell precursor lesions were subjected to logistic regression analysis. RESULTS: hTERC amplification gradually increased with upgrading of dysplasia, reaching the highest level in high-grade intraepithelial neoplasia, and there was a significant difference between the low-grade intraepithelial neoplasia group and the high-grade intraepithelial neoplasia group (P = 0.00). Logistic regression analysis showed that hTERC amplification was correlated with both dysplasia grading and ulcer characteristics of esophageal squamous cell precursor lesions (P < 0.05). CONCLUSIONS: hTERC amplification with increasing grading of esophageal squamous cell precursor lesions and the presence of ulcer characteristics might provide an important molecular and pathological marker for the diagnosis and clinical prognosis of esophageal squamous cell precursor lesions, especially for those ambiguous cases with more divergence in classification. Springer US 2018-10-11 2019 /pmc/articles/PMC6318245/ /pubmed/30311151 http://dx.doi.org/10.1007/s10620-018-5318-7 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Original Article Hu, Yanping Teng, Xiaojing Wu, Linlin Liu, Wei An, Jianduo The Clinicopathological Correlations of hTERC Amplification with Esophageal Squamous Cell Precursor Lesions |
title | The Clinicopathological Correlations of hTERC Amplification with Esophageal Squamous Cell Precursor Lesions |
title_full | The Clinicopathological Correlations of hTERC Amplification with Esophageal Squamous Cell Precursor Lesions |
title_fullStr | The Clinicopathological Correlations of hTERC Amplification with Esophageal Squamous Cell Precursor Lesions |
title_full_unstemmed | The Clinicopathological Correlations of hTERC Amplification with Esophageal Squamous Cell Precursor Lesions |
title_short | The Clinicopathological Correlations of hTERC Amplification with Esophageal Squamous Cell Precursor Lesions |
title_sort | clinicopathological correlations of hterc amplification with esophageal squamous cell precursor lesions |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318245/ https://www.ncbi.nlm.nih.gov/pubmed/30311151 http://dx.doi.org/10.1007/s10620-018-5318-7 |
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