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Metabolic profiling and novel plasma biomarkers for predicting survival in epithelial ovarian cancer

Epithelial ovarian cancer (EOC) is one of the most lethal gynecological malignancies around the world, and patients with ovarian cancer always have an extremely poor chance of survival. Therefore, it is meaningful to develop a highly efficient model that can predict the overall survival for EOC. In...

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Autores principales: Xie, Hongyu, Hou, Yan, Cheng, Jinlong, Openkova, Margarita S., Xia, Bairong, Wang, Wenjie, Li, Ang, Yang, Kai, Li, Junnan, Xu, Huan, Yang, Chunyan, Ma, Libing, Li, Zhenzi, Fan, Xin, Li, Kang, Lou, Ge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458273/
https://www.ncbi.nlm.nih.gov/pubmed/28389631
http://dx.doi.org/10.18632/oncotarget.16739
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author Xie, Hongyu
Hou, Yan
Cheng, Jinlong
Openkova, Margarita S.
Xia, Bairong
Wang, Wenjie
Li, Ang
Yang, Kai
Li, Junnan
Xu, Huan
Yang, Chunyan
Ma, Libing
Li, Zhenzi
Fan, Xin
Li, Kang
Lou, Ge
author_facet Xie, Hongyu
Hou, Yan
Cheng, Jinlong
Openkova, Margarita S.
Xia, Bairong
Wang, Wenjie
Li, Ang
Yang, Kai
Li, Junnan
Xu, Huan
Yang, Chunyan
Ma, Libing
Li, Zhenzi
Fan, Xin
Li, Kang
Lou, Ge
author_sort Xie, Hongyu
collection PubMed
description Epithelial ovarian cancer (EOC) is one of the most lethal gynecological malignancies around the world, and patients with ovarian cancer always have an extremely poor chance of survival. Therefore, it is meaningful to develop a highly efficient model that can predict the overall survival for EOC. In order to investigate whether metabolites could be used to predict the survival of EOC, we performed a metabolic analysis of 98 plasma samples with follow-up information, based on the ultra-performance liquid chromatography mass spectrometry (UPLC/MS) systems in both positive (ESI+) and negative (ESI-) modes. Four metabolites: Kynurenine, Acetylcarnitine, PC (42:11), and LPE(22:0/0:0) were selected as potential predictive biomarkers. The AUC value of metabolite-based risk score, together with pathological stages in predicting three-year survival rate was 0.80. The discrimination performance of these four biomarkers between short-term mortality and long-term survival was excellent, with an AUC value of 0.82. In conclusion, our plasma metabolomics study presented the dysregulated metabolism related to the survival of EOC, and plasma metabolites could be utilized to predict the overall survival and discriminate the short-term mortality and long-term survival for EOC patients. These results could provide supplementary information for further study about EOC survival mechanism and guiding the appropriate clinical treatment.
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spelling pubmed-54582732017-06-08 Metabolic profiling and novel plasma biomarkers for predicting survival in epithelial ovarian cancer Xie, Hongyu Hou, Yan Cheng, Jinlong Openkova, Margarita S. Xia, Bairong Wang, Wenjie Li, Ang Yang, Kai Li, Junnan Xu, Huan Yang, Chunyan Ma, Libing Li, Zhenzi Fan, Xin Li, Kang Lou, Ge Oncotarget Research Paper Epithelial ovarian cancer (EOC) is one of the most lethal gynecological malignancies around the world, and patients with ovarian cancer always have an extremely poor chance of survival. Therefore, it is meaningful to develop a highly efficient model that can predict the overall survival for EOC. In order to investigate whether metabolites could be used to predict the survival of EOC, we performed a metabolic analysis of 98 plasma samples with follow-up information, based on the ultra-performance liquid chromatography mass spectrometry (UPLC/MS) systems in both positive (ESI+) and negative (ESI-) modes. Four metabolites: Kynurenine, Acetylcarnitine, PC (42:11), and LPE(22:0/0:0) were selected as potential predictive biomarkers. The AUC value of metabolite-based risk score, together with pathological stages in predicting three-year survival rate was 0.80. The discrimination performance of these four biomarkers between short-term mortality and long-term survival was excellent, with an AUC value of 0.82. In conclusion, our plasma metabolomics study presented the dysregulated metabolism related to the survival of EOC, and plasma metabolites could be utilized to predict the overall survival and discriminate the short-term mortality and long-term survival for EOC patients. These results could provide supplementary information for further study about EOC survival mechanism and guiding the appropriate clinical treatment. Impact Journals LLC 2017-03-31 /pmc/articles/PMC5458273/ /pubmed/28389631 http://dx.doi.org/10.18632/oncotarget.16739 Text en Copyright: © 2017 Xie et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Xie, Hongyu
Hou, Yan
Cheng, Jinlong
Openkova, Margarita S.
Xia, Bairong
Wang, Wenjie
Li, Ang
Yang, Kai
Li, Junnan
Xu, Huan
Yang, Chunyan
Ma, Libing
Li, Zhenzi
Fan, Xin
Li, Kang
Lou, Ge
Metabolic profiling and novel plasma biomarkers for predicting survival in epithelial ovarian cancer
title Metabolic profiling and novel plasma biomarkers for predicting survival in epithelial ovarian cancer
title_full Metabolic profiling and novel plasma biomarkers for predicting survival in epithelial ovarian cancer
title_fullStr Metabolic profiling and novel plasma biomarkers for predicting survival in epithelial ovarian cancer
title_full_unstemmed Metabolic profiling and novel plasma biomarkers for predicting survival in epithelial ovarian cancer
title_short Metabolic profiling and novel plasma biomarkers for predicting survival in epithelial ovarian cancer
title_sort metabolic profiling and novel plasma biomarkers for predicting survival in epithelial ovarian cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458273/
https://www.ncbi.nlm.nih.gov/pubmed/28389631
http://dx.doi.org/10.18632/oncotarget.16739
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