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Expression of hypoxia-related markers in inflammatory myofibroblastic tumors of the head and neck
BACKGROUND: The etiology of inflammatory myofibroblastic tumors (IMTs) is controversial and the prognosis is unpredictable. Previous studies have not investigated the expression of hypoxia-related markers in IMTs. METHODS: Between 2002 and 2012, 12 consecutive patients with histologically proven IMT...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842822/ https://www.ncbi.nlm.nih.gov/pubmed/24245510 http://dx.doi.org/10.1186/1477-7819-11-294 |
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author | Wang, Kui-Rong Jiang, Tao Wu, Ting-Ting Zhou, Shui-Hong Yao, Hong-Tian Wang, Qin-Ying Lu, Zhong-Jie |
author_facet | Wang, Kui-Rong Jiang, Tao Wu, Ting-Ting Zhou, Shui-Hong Yao, Hong-Tian Wang, Qin-Ying Lu, Zhong-Jie |
author_sort | Wang, Kui-Rong |
collection | PubMed |
description | BACKGROUND: The etiology of inflammatory myofibroblastic tumors (IMTs) is controversial and the prognosis is unpredictable. Previous studies have not investigated the expression of hypoxia-related markers in IMTs. METHODS: Between 2002 and 2012, 12 consecutive patients with histologically proven IMTs were enrolled in the study. Immunohistochemistry was used to detect GLUT-1, HIF-1α, PI3K, and p-Akt expression in paraffin-embedded tumor specimens. Associations among GLUT-1, HIF-1α, PI3K, and p-Akt protein expression and clinical parameters were investigated. RESULTS: The mean duration of follow-up was 52.1 months (range, 11 to 132 months). Six patients had local recurrence. GLUT-1, HIF-1α, PI3K, and p-Akt expression were detected in 41.7%, 50.0%, 33.3%, and 41.7% of patients, respectively. Fisher’s exact test revealed significant correlations between recurrence of IMT and PI3K expression (P = 0.01) and p-Akt expression (P = 0.015). Univariate analyses revealed significant correlations between survival and GLUT-1 expression (P = 0.028), PI3K expression (P = 0.006), and p-Akt expression (P = 0.028). Multivariate analysis did not show a significant relationship between survival and GLUT-1, HIF-1α, PI3K, or p-Akt. Spearman rank correlation analysis showed significant correlations between HIF-1α and PI3K expression (r = 0.707, P = 0.01) and between p-Akt and PI3K expression (r = 0.837, P = 0.001). CONCLUSIONS: Although our results are inconclusive owing to the small sample size, they suggest that PI3K and p-Akt expression may play a role in the recurrence of IMTs of the head and neck. |
format | Online Article Text |
id | pubmed-3842822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38428222013-11-29 Expression of hypoxia-related markers in inflammatory myofibroblastic tumors of the head and neck Wang, Kui-Rong Jiang, Tao Wu, Ting-Ting Zhou, Shui-Hong Yao, Hong-Tian Wang, Qin-Ying Lu, Zhong-Jie World J Surg Oncol Research BACKGROUND: The etiology of inflammatory myofibroblastic tumors (IMTs) is controversial and the prognosis is unpredictable. Previous studies have not investigated the expression of hypoxia-related markers in IMTs. METHODS: Between 2002 and 2012, 12 consecutive patients with histologically proven IMTs were enrolled in the study. Immunohistochemistry was used to detect GLUT-1, HIF-1α, PI3K, and p-Akt expression in paraffin-embedded tumor specimens. Associations among GLUT-1, HIF-1α, PI3K, and p-Akt protein expression and clinical parameters were investigated. RESULTS: The mean duration of follow-up was 52.1 months (range, 11 to 132 months). Six patients had local recurrence. GLUT-1, HIF-1α, PI3K, and p-Akt expression were detected in 41.7%, 50.0%, 33.3%, and 41.7% of patients, respectively. Fisher’s exact test revealed significant correlations between recurrence of IMT and PI3K expression (P = 0.01) and p-Akt expression (P = 0.015). Univariate analyses revealed significant correlations between survival and GLUT-1 expression (P = 0.028), PI3K expression (P = 0.006), and p-Akt expression (P = 0.028). Multivariate analysis did not show a significant relationship between survival and GLUT-1, HIF-1α, PI3K, or p-Akt. Spearman rank correlation analysis showed significant correlations between HIF-1α and PI3K expression (r = 0.707, P = 0.01) and between p-Akt and PI3K expression (r = 0.837, P = 0.001). CONCLUSIONS: Although our results are inconclusive owing to the small sample size, they suggest that PI3K and p-Akt expression may play a role in the recurrence of IMTs of the head and neck. BioMed Central 2013-11-19 /pmc/articles/PMC3842822/ /pubmed/24245510 http://dx.doi.org/10.1186/1477-7819-11-294 Text en Copyright © 2013 Wang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Wang, Kui-Rong Jiang, Tao Wu, Ting-Ting Zhou, Shui-Hong Yao, Hong-Tian Wang, Qin-Ying Lu, Zhong-Jie Expression of hypoxia-related markers in inflammatory myofibroblastic tumors of the head and neck |
title | Expression of hypoxia-related markers in inflammatory myofibroblastic tumors of the head and neck |
title_full | Expression of hypoxia-related markers in inflammatory myofibroblastic tumors of the head and neck |
title_fullStr | Expression of hypoxia-related markers in inflammatory myofibroblastic tumors of the head and neck |
title_full_unstemmed | Expression of hypoxia-related markers in inflammatory myofibroblastic tumors of the head and neck |
title_short | Expression of hypoxia-related markers in inflammatory myofibroblastic tumors of the head and neck |
title_sort | expression of hypoxia-related markers in inflammatory myofibroblastic tumors of the head and neck |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842822/ https://www.ncbi.nlm.nih.gov/pubmed/24245510 http://dx.doi.org/10.1186/1477-7819-11-294 |
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