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Low expression of mixed lineage kinase domain-like protein is associated with poor prognosis in ovarian cancer patients
BACKGROUND: Mixed lineage kinase domain-like protein (MLKL) was initially identified as a key receptor interacting protein 3 downstream component of tumor-necrosis-factor-induced necrosis. In this study, we characterized the expression of MLKL in ovarian carcinomas and evaluated the prognostic value...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817086/ https://www.ncbi.nlm.nih.gov/pubmed/24204164 http://dx.doi.org/10.2147/OTT.S52805 |
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author | He, Ling Peng, Kuan Liu, Yizhi Xiong, Jing Zhu, Fu-fan |
author_facet | He, Ling Peng, Kuan Liu, Yizhi Xiong, Jing Zhu, Fu-fan |
author_sort | He, Ling |
collection | PubMed |
description | BACKGROUND: Mixed lineage kinase domain-like protein (MLKL) was initially identified as a key receptor interacting protein 3 downstream component of tumor-necrosis-factor-induced necrosis. In this study, we characterized the expression of MLKL in ovarian carcinomas and evaluated the prognostic value of MLKL in patients with ovarian cancer. MATERIALS AND METHODS: The ovarian cancer tissue specimens were collected from 153 patients diagnosed as primary ovarian cancer after operation at The Second Xiangya Hospital from January 2005 to December 2008. Immunohistochemistry was performed for MLKL and the protein expression score was quantified using an established scoring system. Kaplan–Meier survival curves were generated for disease-free survival (DFS) and overall survival (OS) for all patients. MLKL expression levels were correlated with DFS and OS using univariate and multivariate Cox regression analysis. RESULTS: Seventy-five patients (49%) were defined as having high MLKL expression and 67 patients (43.7%) had >80% of cells staining for MLKL. Remarkably, low MLKL expression was significantly associated with decreased DFS (median 40 months versus 25 months, P=0.0282) and OS (median 43 months versus 28 months, P=0.0032). In multivariate analysis, retained significance was also observed. CONCLUSION: Low MLKL expression was significantly associated with both decreased DFS and OS in patients with primary ovarian cancer. MLKL expression may serve as a potential prognostic marker in patients with ovarian cancer. |
format | Online Article Text |
id | pubmed-3817086 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38170862013-11-07 Low expression of mixed lineage kinase domain-like protein is associated with poor prognosis in ovarian cancer patients He, Ling Peng, Kuan Liu, Yizhi Xiong, Jing Zhu, Fu-fan Onco Targets Ther Short Report BACKGROUND: Mixed lineage kinase domain-like protein (MLKL) was initially identified as a key receptor interacting protein 3 downstream component of tumor-necrosis-factor-induced necrosis. In this study, we characterized the expression of MLKL in ovarian carcinomas and evaluated the prognostic value of MLKL in patients with ovarian cancer. MATERIALS AND METHODS: The ovarian cancer tissue specimens were collected from 153 patients diagnosed as primary ovarian cancer after operation at The Second Xiangya Hospital from January 2005 to December 2008. Immunohistochemistry was performed for MLKL and the protein expression score was quantified using an established scoring system. Kaplan–Meier survival curves were generated for disease-free survival (DFS) and overall survival (OS) for all patients. MLKL expression levels were correlated with DFS and OS using univariate and multivariate Cox regression analysis. RESULTS: Seventy-five patients (49%) were defined as having high MLKL expression and 67 patients (43.7%) had >80% of cells staining for MLKL. Remarkably, low MLKL expression was significantly associated with decreased DFS (median 40 months versus 25 months, P=0.0282) and OS (median 43 months versus 28 months, P=0.0032). In multivariate analysis, retained significance was also observed. CONCLUSION: Low MLKL expression was significantly associated with both decreased DFS and OS in patients with primary ovarian cancer. MLKL expression may serve as a potential prognostic marker in patients with ovarian cancer. Dove Medical Press 2013-10-30 /pmc/articles/PMC3817086/ /pubmed/24204164 http://dx.doi.org/10.2147/OTT.S52805 Text en © 2013 He et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Short Report He, Ling Peng, Kuan Liu, Yizhi Xiong, Jing Zhu, Fu-fan Low expression of mixed lineage kinase domain-like protein is associated with poor prognosis in ovarian cancer patients |
title | Low expression of mixed lineage kinase domain-like protein is associated with poor prognosis in ovarian cancer patients |
title_full | Low expression of mixed lineage kinase domain-like protein is associated with poor prognosis in ovarian cancer patients |
title_fullStr | Low expression of mixed lineage kinase domain-like protein is associated with poor prognosis in ovarian cancer patients |
title_full_unstemmed | Low expression of mixed lineage kinase domain-like protein is associated with poor prognosis in ovarian cancer patients |
title_short | Low expression of mixed lineage kinase domain-like protein is associated with poor prognosis in ovarian cancer patients |
title_sort | low expression of mixed lineage kinase domain-like protein is associated with poor prognosis in ovarian cancer patients |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817086/ https://www.ncbi.nlm.nih.gov/pubmed/24204164 http://dx.doi.org/10.2147/OTT.S52805 |
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