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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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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. |
format | Online Article Text |
id | pubmed-3438113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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