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Expression of the interleukin-21 and phosphorylated extracellular signal regulated kinase 1/2 in Kimura disease

OBJECTIVE: To investigate the expressions of interleukin (IL)-21 and phosphorylated extracellular signal regulated kinase 1/2 (pERK1/2) in Kimura disease (KD) and to correlate the findings with clinical and prognostic variables. METHODS: Immunohistochemical analysis of IL-21 and pERK1/2 was performe...

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Autores principales: Chen, Qing-li, Li, Chen-xi, Shao, Bo, Gong, Zhong-cheng, Liu, Hui, Ling, Bin, Abasi, Keremu, Hu, Lu-lu, Wang, Bing, Yin, Xiao-peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537556/
https://www.ncbi.nlm.nih.gov/pubmed/28108473
http://dx.doi.org/10.1136/jclinpath-2016-204096
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author Chen, Qing-li
Li, Chen-xi
Shao, Bo
Gong, Zhong-cheng
Liu, Hui
Ling, Bin
Abasi, Keremu
Hu, Lu-lu
Wang, Bing
Yin, Xiao-peng
author_facet Chen, Qing-li
Li, Chen-xi
Shao, Bo
Gong, Zhong-cheng
Liu, Hui
Ling, Bin
Abasi, Keremu
Hu, Lu-lu
Wang, Bing
Yin, Xiao-peng
author_sort Chen, Qing-li
collection PubMed
description OBJECTIVE: To investigate the expressions of interleukin (IL)-21 and phosphorylated extracellular signal regulated kinase 1/2 (pERK1/2) in Kimura disease (KD) and to correlate the findings with clinical and prognostic variables. METHODS: Immunohistochemical analysis of IL-21 and pERK1/2 was performed in 18 cases of KD and five gender- and age-matched control samples. Clinical data were extracted and patients followed up for a mean period of 32.1 months. RESULTS: After a mean follow-up period of 32.1 months (range 1–102 months), recurrence was diagnosed as the end point for seven patients—that is, a 44% (7/16) cumulative recurrence rate. In comparison with gender- and age-matched controls, patients showed strong in situ expressions of IL-21 and pERK1/2, respectively (p<0.05). Patients with strong IL-21 staining intensity and overexpression of pERK1/2 had a lower recurrence rate than those with moderate staining intensity (p=0.049, p=0.019, respectively). However, differences were not statistically significant by gender, age, eosinophils, location, multiplicity, laterality, size, duration and primary outbreak. pERK1/2 was the independent prognostic factor (p=0.020), while age, gender, eosinophils, multiplicity, laterality, size, duration, primary outbreak and expression of IL-21 were not. CONCLUSIONS: This study suggests that the IL-21/pERK1/2 pathway is activated in KD, and pERK1/2 might be considered as a potential prognostic indicator in KD.
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spelling pubmed-55375562017-08-03 Expression of the interleukin-21 and phosphorylated extracellular signal regulated kinase 1/2 in Kimura disease Chen, Qing-li Li, Chen-xi Shao, Bo Gong, Zhong-cheng Liu, Hui Ling, Bin Abasi, Keremu Hu, Lu-lu Wang, Bing Yin, Xiao-peng J Clin Pathol Original Article OBJECTIVE: To investigate the expressions of interleukin (IL)-21 and phosphorylated extracellular signal regulated kinase 1/2 (pERK1/2) in Kimura disease (KD) and to correlate the findings with clinical and prognostic variables. METHODS: Immunohistochemical analysis of IL-21 and pERK1/2 was performed in 18 cases of KD and five gender- and age-matched control samples. Clinical data were extracted and patients followed up for a mean period of 32.1 months. RESULTS: After a mean follow-up period of 32.1 months (range 1–102 months), recurrence was diagnosed as the end point for seven patients—that is, a 44% (7/16) cumulative recurrence rate. In comparison with gender- and age-matched controls, patients showed strong in situ expressions of IL-21 and pERK1/2, respectively (p<0.05). Patients with strong IL-21 staining intensity and overexpression of pERK1/2 had a lower recurrence rate than those with moderate staining intensity (p=0.049, p=0.019, respectively). However, differences were not statistically significant by gender, age, eosinophils, location, multiplicity, laterality, size, duration and primary outbreak. pERK1/2 was the independent prognostic factor (p=0.020), while age, gender, eosinophils, multiplicity, laterality, size, duration, primary outbreak and expression of IL-21 were not. CONCLUSIONS: This study suggests that the IL-21/pERK1/2 pathway is activated in KD, and pERK1/2 might be considered as a potential prognostic indicator in KD. BMJ Publishing Group 2017-08 2017-01-20 /pmc/articles/PMC5537556/ /pubmed/28108473 http://dx.doi.org/10.1136/jclinpath-2016-204096 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Original Article
Chen, Qing-li
Li, Chen-xi
Shao, Bo
Gong, Zhong-cheng
Liu, Hui
Ling, Bin
Abasi, Keremu
Hu, Lu-lu
Wang, Bing
Yin, Xiao-peng
Expression of the interleukin-21 and phosphorylated extracellular signal regulated kinase 1/2 in Kimura disease
title Expression of the interleukin-21 and phosphorylated extracellular signal regulated kinase 1/2 in Kimura disease
title_full Expression of the interleukin-21 and phosphorylated extracellular signal regulated kinase 1/2 in Kimura disease
title_fullStr Expression of the interleukin-21 and phosphorylated extracellular signal regulated kinase 1/2 in Kimura disease
title_full_unstemmed Expression of the interleukin-21 and phosphorylated extracellular signal regulated kinase 1/2 in Kimura disease
title_short Expression of the interleukin-21 and phosphorylated extracellular signal regulated kinase 1/2 in Kimura disease
title_sort expression of the interleukin-21 and phosphorylated extracellular signal regulated kinase 1/2 in kimura disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537556/
https://www.ncbi.nlm.nih.gov/pubmed/28108473
http://dx.doi.org/10.1136/jclinpath-2016-204096
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