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Prognostic significance of MyD88 expression by human epithelial ovarian carcinoma cells

BACKGROUND: MyD88 is an adaptor protein for TLR-4 signaling known to mediate paclitaxel resistance in epithelial ovarian carcinoma (EOC). This study examined the clinical significance of MyD88 expression in EOC. METHODS: MyD88 and TLR-4 expression were examined by immunocytochemistry in 109 specimen...

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Autores principales: Zhu, Yi, Huang, Jian-Ming, Zhang, Guo-Nan, Zha, Xiao, Deng, Bi-Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3438113/
https://www.ncbi.nlm.nih.gov/pubmed/22533866
http://dx.doi.org/10.1186/1479-5876-10-77
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author Zhu, Yi
Huang, Jian-Ming
Zhang, Guo-Nan
Zha, Xiao
Deng, Bi-Fang
author_facet Zhu, Yi
Huang, Jian-Ming
Zhang, Guo-Nan
Zha, Xiao
Deng, Bi-Fang
author_sort Zhu, Yi
collection PubMed
description BACKGROUND: MyD88 is an adaptor protein for TLR-4 signaling known to mediate paclitaxel resistance in epithelial ovarian carcinoma (EOC). This study examined the clinical significance of MyD88 expression in EOC. METHODS: MyD88 and TLR-4 expression were examined by immunocytochemistry in 109 specimens of ovarian tissues, comprising EOC (N = 83), borderline tumors (N = 9), benign cysts (N = 9) and normal ovarian tissue (N = 8), and clinical data collected by a retrospective chart review. The correlations between MyD88 expression and clinicopathological factors and outcomes were analyzed. RESULTS: TLR-4 expression was detected frequently in all the ovarian tissues. Distinct MyD88 expression was showed in EOC (64 of 83, 77.1 %), in borderline tumors (5 of 9, 55.6 %) and in benign cysts (3 of 9, 33.3 %), and normal ovarian tissue showed no MyD88 expression. Positive MyD88 expression significantly correlated with shorter disease-free and overall survival for EOC (P < 0.0001 and P = 0.0031), and high MyD88 expression was significantly correlated with tumor metastasis (P = 0.0012) for EOC. Univariate and multivariate analyses revealed that MyD88 expression was an independent prognostic factor for disease-free survival and overall survival for EOC. CONCLUSION: Our data indicate that MyD88 expression is a significantly poor prognostic factor for EOC. A better understanding of the role of MyD88 expression in disease progression and outcome may be helpful for development of novel chemotherapies for patients with EOC.
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spelling pubmed-34381132012-09-11 Prognostic significance of MyD88 expression by human epithelial ovarian carcinoma cells Zhu, Yi Huang, Jian-Ming Zhang, Guo-Nan Zha, Xiao Deng, Bi-Fang J Transl Med Research BACKGROUND: MyD88 is an adaptor protein for TLR-4 signaling known to mediate paclitaxel resistance in epithelial ovarian carcinoma (EOC). This study examined the clinical significance of MyD88 expression in EOC. METHODS: MyD88 and TLR-4 expression were examined by immunocytochemistry in 109 specimens of ovarian tissues, comprising EOC (N = 83), borderline tumors (N = 9), benign cysts (N = 9) and normal ovarian tissue (N = 8), and clinical data collected by a retrospective chart review. The correlations between MyD88 expression and clinicopathological factors and outcomes were analyzed. RESULTS: TLR-4 expression was detected frequently in all the ovarian tissues. Distinct MyD88 expression was showed in EOC (64 of 83, 77.1 %), in borderline tumors (5 of 9, 55.6 %) and in benign cysts (3 of 9, 33.3 %), and normal ovarian tissue showed no MyD88 expression. Positive MyD88 expression significantly correlated with shorter disease-free and overall survival for EOC (P < 0.0001 and P = 0.0031), and high MyD88 expression was significantly correlated with tumor metastasis (P = 0.0012) for EOC. Univariate and multivariate analyses revealed that MyD88 expression was an independent prognostic factor for disease-free survival and overall survival for EOC. CONCLUSION: Our data indicate that MyD88 expression is a significantly poor prognostic factor for EOC. A better understanding of the role of MyD88 expression in disease progression and outcome may be helpful for development of novel chemotherapies for patients with EOC. BioMed Central 2012-04-25 /pmc/articles/PMC3438113/ /pubmed/22533866 http://dx.doi.org/10.1186/1479-5876-10-77 Text en Copyright ©2012 Zhu 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
Zhu, Yi
Huang, Jian-Ming
Zhang, Guo-Nan
Zha, Xiao
Deng, Bi-Fang
Prognostic significance of MyD88 expression by human epithelial ovarian carcinoma cells
title Prognostic significance of MyD88 expression by human epithelial ovarian carcinoma cells
title_full Prognostic significance of MyD88 expression by human epithelial ovarian carcinoma cells
title_fullStr Prognostic significance of MyD88 expression by human epithelial ovarian carcinoma cells
title_full_unstemmed Prognostic significance of MyD88 expression by human epithelial ovarian carcinoma cells
title_short Prognostic significance of MyD88 expression by human epithelial ovarian carcinoma cells
title_sort prognostic significance of myd88 expression by human epithelial ovarian carcinoma cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3438113/
https://www.ncbi.nlm.nih.gov/pubmed/22533866
http://dx.doi.org/10.1186/1479-5876-10-77
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