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Clinical significance of COL1A1 and COL1A2 expression levels in hypopharyngeal squamous cell carcinoma
Alterations in collagen type I α1 (COL1A1) and collagen type I α 2 (COL1A2) expression levels have been reported to predict prognosis in various types of cancer. However, the effect of these biomarkers on hypopharyngeal squamous cell carcinoma (HPSCC) is yet to be fully elucidated. The present study...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7285875/ https://www.ncbi.nlm.nih.gov/pubmed/32566007 http://dx.doi.org/10.3892/ol.2020.11594 |
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author | Lin, Peiliang Tian, Peng Pang, Jiaqi Lai, Lan He, Gui Song, Yang Zheng, Yiqing |
author_facet | Lin, Peiliang Tian, Peng Pang, Jiaqi Lai, Lan He, Gui Song, Yang Zheng, Yiqing |
author_sort | Lin, Peiliang |
collection | PubMed |
description | Alterations in collagen type I α1 (COL1A1) and collagen type I α 2 (COL1A2) expression levels have been reported to predict prognosis in various types of cancer. However, the effect of these biomarkers on hypopharyngeal squamous cell carcinoma (HPSCC) is yet to be fully elucidated. The present study aimed to explore the prognostic significance of COL1A1 and COL1A2 expression levels in HPSCC. The expression levels of COL1A1 and COL1A2 in 67 patients with HPSCC were examined using an immunohistochemical assay in a tissue microarray. The associations between COL1A1/COL1A2 expression levels and patient clinicopathological features were analyzed using ANOVA, Pearson's χ(2) or Fisher's exact test. The Cox proportional hazard models and Kaplan-Meier survival analysis with log-rank tests were used to analyze the significance of COL1A1/COL1A2 as prognostic markers for patients with HPSCC. As a result, immunohistochemical staining revealed that COL1A1 was positively expressed in all cases, among which 40.3% were strong positive, while COL1A2 was positively expressed in 76.1% of the HPSCC cases with 6.0% of the samples exhibiting strong staining. Further analysis revealed no significant association between the expression levels of COL1A1/COL1A2 and other clinicopathological features. Cox regression analysis revealed that a high COL1A2 expression level predicted a high locoregional recurrence and a less favorable disease-free survival rate (P=0.042 and 0.020, respectively). Overall, the present study indicated that COL1A2 expression levels may have value as a prognostic indicator in HPSCC. |
format | Online Article Text |
id | pubmed-7285875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-72858752020-06-18 Clinical significance of COL1A1 and COL1A2 expression levels in hypopharyngeal squamous cell carcinoma Lin, Peiliang Tian, Peng Pang, Jiaqi Lai, Lan He, Gui Song, Yang Zheng, Yiqing Oncol Lett Articles Alterations in collagen type I α1 (COL1A1) and collagen type I α 2 (COL1A2) expression levels have been reported to predict prognosis in various types of cancer. However, the effect of these biomarkers on hypopharyngeal squamous cell carcinoma (HPSCC) is yet to be fully elucidated. The present study aimed to explore the prognostic significance of COL1A1 and COL1A2 expression levels in HPSCC. The expression levels of COL1A1 and COL1A2 in 67 patients with HPSCC were examined using an immunohistochemical assay in a tissue microarray. The associations between COL1A1/COL1A2 expression levels and patient clinicopathological features were analyzed using ANOVA, Pearson's χ(2) or Fisher's exact test. The Cox proportional hazard models and Kaplan-Meier survival analysis with log-rank tests were used to analyze the significance of COL1A1/COL1A2 as prognostic markers for patients with HPSCC. As a result, immunohistochemical staining revealed that COL1A1 was positively expressed in all cases, among which 40.3% were strong positive, while COL1A2 was positively expressed in 76.1% of the HPSCC cases with 6.0% of the samples exhibiting strong staining. Further analysis revealed no significant association between the expression levels of COL1A1/COL1A2 and other clinicopathological features. Cox regression analysis revealed that a high COL1A2 expression level predicted a high locoregional recurrence and a less favorable disease-free survival rate (P=0.042 and 0.020, respectively). Overall, the present study indicated that COL1A2 expression levels may have value as a prognostic indicator in HPSCC. D.A. Spandidos 2020-07 2020-05-07 /pmc/articles/PMC7285875/ /pubmed/32566007 http://dx.doi.org/10.3892/ol.2020.11594 Text en Copyright: © Lin et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Lin, Peiliang Tian, Peng Pang, Jiaqi Lai, Lan He, Gui Song, Yang Zheng, Yiqing Clinical significance of COL1A1 and COL1A2 expression levels in hypopharyngeal squamous cell carcinoma |
title | Clinical significance of COL1A1 and COL1A2 expression levels in hypopharyngeal squamous cell carcinoma |
title_full | Clinical significance of COL1A1 and COL1A2 expression levels in hypopharyngeal squamous cell carcinoma |
title_fullStr | Clinical significance of COL1A1 and COL1A2 expression levels in hypopharyngeal squamous cell carcinoma |
title_full_unstemmed | Clinical significance of COL1A1 and COL1A2 expression levels in hypopharyngeal squamous cell carcinoma |
title_short | Clinical significance of COL1A1 and COL1A2 expression levels in hypopharyngeal squamous cell carcinoma |
title_sort | clinical significance of col1a1 and col1a2 expression levels in hypopharyngeal squamous cell carcinoma |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7285875/ https://www.ncbi.nlm.nih.gov/pubmed/32566007 http://dx.doi.org/10.3892/ol.2020.11594 |
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