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Identification of F5 as a Prognostic Biomarker in Patients with Gastric Cancer

Association of Coagulation factor V (F5) polymorphisms with the occurrence of many types of cancers has been widely reported, but whether it is of prognostic relevance in some cancers remain to be resolved. The RNA-sequencing dataset was downloaded from The Cancer Genome Atlas (TCGA). The potential...

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Autores principales: Liu, Yi, Liao, Xi-Wen, Qin, Yu-Zhou, Mo, Xian-Wei, Luo, Shan-Shan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7064826/
https://www.ncbi.nlm.nih.gov/pubmed/32190689
http://dx.doi.org/10.1155/2020/9280841
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author Liu, Yi
Liao, Xi-Wen
Qin, Yu-Zhou
Mo, Xian-Wei
Luo, Shan-Shan
author_facet Liu, Yi
Liao, Xi-Wen
Qin, Yu-Zhou
Mo, Xian-Wei
Luo, Shan-Shan
author_sort Liu, Yi
collection PubMed
description Association of Coagulation factor V (F5) polymorphisms with the occurrence of many types of cancers has been widely reported, but whether it is of prognostic relevance in some cancers remain to be resolved. The RNA-sequencing dataset was downloaded from The Cancer Genome Atlas (TCGA). The potential of F5 genes to predict the survival time of gastric cancer (GC) patients was investigated using univariate and multivariate survival analysis whereas “Kaplan-Meier plotter” (KM-plotter) online tools were employed to validate the outcomes. TCGA data revealed that F5 mRNA levels were significantly upregulated in gastric cancer samples. Survival analysis confirmed that high levels of F5 mRNA correlated with short overall survival (OS) in gastric cancer patients, and the area under the curve (AUC) values of 1-, 2-, and 5-year OS rate were 0.554, 0.593, and 0.603, respectively. Survival analysis by KM-plotter indicated that the high expression of F5 mRNA was significantly associated with a shorter OS compared with the low expression level in all patients with GC, and this was also the case for patients in stage III (hazard ratio (HR) = 1.78, P = 0.017). These findings suggest that the F5 gene is significantly upregulated in GC tumour tissues, and may be a potential prognostic biomarker for GC.
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spelling pubmed-70648262020-03-18 Identification of F5 as a Prognostic Biomarker in Patients with Gastric Cancer Liu, Yi Liao, Xi-Wen Qin, Yu-Zhou Mo, Xian-Wei Luo, Shan-Shan Biomed Res Int Research Article Association of Coagulation factor V (F5) polymorphisms with the occurrence of many types of cancers has been widely reported, but whether it is of prognostic relevance in some cancers remain to be resolved. The RNA-sequencing dataset was downloaded from The Cancer Genome Atlas (TCGA). The potential of F5 genes to predict the survival time of gastric cancer (GC) patients was investigated using univariate and multivariate survival analysis whereas “Kaplan-Meier plotter” (KM-plotter) online tools were employed to validate the outcomes. TCGA data revealed that F5 mRNA levels were significantly upregulated in gastric cancer samples. Survival analysis confirmed that high levels of F5 mRNA correlated with short overall survival (OS) in gastric cancer patients, and the area under the curve (AUC) values of 1-, 2-, and 5-year OS rate were 0.554, 0.593, and 0.603, respectively. Survival analysis by KM-plotter indicated that the high expression of F5 mRNA was significantly associated with a shorter OS compared with the low expression level in all patients with GC, and this was also the case for patients in stage III (hazard ratio (HR) = 1.78, P = 0.017). These findings suggest that the F5 gene is significantly upregulated in GC tumour tissues, and may be a potential prognostic biomarker for GC. Hindawi 2020-02-27 /pmc/articles/PMC7064826/ /pubmed/32190689 http://dx.doi.org/10.1155/2020/9280841 Text en Copyright © 2020 Yi Liu et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Liu, Yi
Liao, Xi-Wen
Qin, Yu-Zhou
Mo, Xian-Wei
Luo, Shan-Shan
Identification of F5 as a Prognostic Biomarker in Patients with Gastric Cancer
title Identification of F5 as a Prognostic Biomarker in Patients with Gastric Cancer
title_full Identification of F5 as a Prognostic Biomarker in Patients with Gastric Cancer
title_fullStr Identification of F5 as a Prognostic Biomarker in Patients with Gastric Cancer
title_full_unstemmed Identification of F5 as a Prognostic Biomarker in Patients with Gastric Cancer
title_short Identification of F5 as a Prognostic Biomarker in Patients with Gastric Cancer
title_sort identification of f5 as a prognostic biomarker in patients with gastric cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7064826/
https://www.ncbi.nlm.nih.gov/pubmed/32190689
http://dx.doi.org/10.1155/2020/9280841
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