Cargando…
A Novel Clinical Six-Flavoprotein-Gene Signature Predicts Prognosis in Esophageal Squamous Cell Carcinoma
Flavoproteins and their interacting proteins play important roles in mitochondrial electron transport, fatty acid degradation, and redox regulation. However, their clinical significance and function in esophageal squamous cell carcinoma (ESCC) are little known. Here, using survival analysis and mach...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878914/ https://www.ncbi.nlm.nih.gov/pubmed/31815134 http://dx.doi.org/10.1155/2019/3869825 |
_version_ | 1783473532197404672 |
---|---|
author | Peng, Liu Guo, Jin-Cheng Long, Lin Pan, Feng Zhao, Jian-Mei Xu, Li-Yan Li, En-Min |
author_facet | Peng, Liu Guo, Jin-Cheng Long, Lin Pan, Feng Zhao, Jian-Mei Xu, Li-Yan Li, En-Min |
author_sort | Peng, Liu |
collection | PubMed |
description | Flavoproteins and their interacting proteins play important roles in mitochondrial electron transport, fatty acid degradation, and redox regulation. However, their clinical significance and function in esophageal squamous cell carcinoma (ESCC) are little known. Here, using survival analysis and machine learning, we mined 179 patient expression profiles with ESCC in GSE53625 from the Gene Expression Omnibus (GEO) database and constructed a signature consisting of two flavoprotein genes (GPD2 and PYROXD2) and four flavoprotein interacting protein genes (CTTN, GGH, SRC, and SYNJ2BP). Kaplan–Meier analysis revealed the signature was significantly associated with the survival of ESCC patients (mean survival time: 26.77 months in the high-risk group vs. 54.97 months in the low-risk group, P < 0.001, n = 179), and time-dependent ROC analysis demonstrated that the six-gene signature had good predictive ability for six-year survival for ESCC (AUC = 0.86, 95% CI: 0.81–0.90). We then validated its prediction performance in an independent set by RT-PCR (mean survival: 15.73 months in the high-risk group vs. 21.1 months in the low-risk group, P=0.032, n = 121). Furthermore, RNAi-mediated knockdown of genes in the flavoprotein signature led to decreased proliferation and migration of ESCC cells. Taken together, CTTN, GGH, GPD2, PYROXD2, SRC, and SYNJ2BP have an important clinical significance for prognosis of ESCC patients, suggesting they are efficient prognostic markers and potential targets for ESCC therapy. |
format | Online Article Text |
id | pubmed-6878914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-68789142019-12-08 A Novel Clinical Six-Flavoprotein-Gene Signature Predicts Prognosis in Esophageal Squamous Cell Carcinoma Peng, Liu Guo, Jin-Cheng Long, Lin Pan, Feng Zhao, Jian-Mei Xu, Li-Yan Li, En-Min Biomed Res Int Research Article Flavoproteins and their interacting proteins play important roles in mitochondrial electron transport, fatty acid degradation, and redox regulation. However, their clinical significance and function in esophageal squamous cell carcinoma (ESCC) are little known. Here, using survival analysis and machine learning, we mined 179 patient expression profiles with ESCC in GSE53625 from the Gene Expression Omnibus (GEO) database and constructed a signature consisting of two flavoprotein genes (GPD2 and PYROXD2) and four flavoprotein interacting protein genes (CTTN, GGH, SRC, and SYNJ2BP). Kaplan–Meier analysis revealed the signature was significantly associated with the survival of ESCC patients (mean survival time: 26.77 months in the high-risk group vs. 54.97 months in the low-risk group, P < 0.001, n = 179), and time-dependent ROC analysis demonstrated that the six-gene signature had good predictive ability for six-year survival for ESCC (AUC = 0.86, 95% CI: 0.81–0.90). We then validated its prediction performance in an independent set by RT-PCR (mean survival: 15.73 months in the high-risk group vs. 21.1 months in the low-risk group, P=0.032, n = 121). Furthermore, RNAi-mediated knockdown of genes in the flavoprotein signature led to decreased proliferation and migration of ESCC cells. Taken together, CTTN, GGH, GPD2, PYROXD2, SRC, and SYNJ2BP have an important clinical significance for prognosis of ESCC patients, suggesting they are efficient prognostic markers and potential targets for ESCC therapy. Hindawi 2019-10-30 /pmc/articles/PMC6878914/ /pubmed/31815134 http://dx.doi.org/10.1155/2019/3869825 Text en Copyright © 2019 Liu Peng 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 Peng, Liu Guo, Jin-Cheng Long, Lin Pan, Feng Zhao, Jian-Mei Xu, Li-Yan Li, En-Min A Novel Clinical Six-Flavoprotein-Gene Signature Predicts Prognosis in Esophageal Squamous Cell Carcinoma |
title | A Novel Clinical Six-Flavoprotein-Gene Signature Predicts Prognosis in Esophageal Squamous Cell Carcinoma |
title_full | A Novel Clinical Six-Flavoprotein-Gene Signature Predicts Prognosis in Esophageal Squamous Cell Carcinoma |
title_fullStr | A Novel Clinical Six-Flavoprotein-Gene Signature Predicts Prognosis in Esophageal Squamous Cell Carcinoma |
title_full_unstemmed | A Novel Clinical Six-Flavoprotein-Gene Signature Predicts Prognosis in Esophageal Squamous Cell Carcinoma |
title_short | A Novel Clinical Six-Flavoprotein-Gene Signature Predicts Prognosis in Esophageal Squamous Cell Carcinoma |
title_sort | novel clinical six-flavoprotein-gene signature predicts prognosis in esophageal squamous cell carcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878914/ https://www.ncbi.nlm.nih.gov/pubmed/31815134 http://dx.doi.org/10.1155/2019/3869825 |
work_keys_str_mv | AT pengliu anovelclinicalsixflavoproteingenesignaturepredictsprognosisinesophagealsquamouscellcarcinoma AT guojincheng anovelclinicalsixflavoproteingenesignaturepredictsprognosisinesophagealsquamouscellcarcinoma AT longlin anovelclinicalsixflavoproteingenesignaturepredictsprognosisinesophagealsquamouscellcarcinoma AT panfeng anovelclinicalsixflavoproteingenesignaturepredictsprognosisinesophagealsquamouscellcarcinoma AT zhaojianmei anovelclinicalsixflavoproteingenesignaturepredictsprognosisinesophagealsquamouscellcarcinoma AT xuliyan anovelclinicalsixflavoproteingenesignaturepredictsprognosisinesophagealsquamouscellcarcinoma AT lienmin anovelclinicalsixflavoproteingenesignaturepredictsprognosisinesophagealsquamouscellcarcinoma AT pengliu novelclinicalsixflavoproteingenesignaturepredictsprognosisinesophagealsquamouscellcarcinoma AT guojincheng novelclinicalsixflavoproteingenesignaturepredictsprognosisinesophagealsquamouscellcarcinoma AT longlin novelclinicalsixflavoproteingenesignaturepredictsprognosisinesophagealsquamouscellcarcinoma AT panfeng novelclinicalsixflavoproteingenesignaturepredictsprognosisinesophagealsquamouscellcarcinoma AT zhaojianmei novelclinicalsixflavoproteingenesignaturepredictsprognosisinesophagealsquamouscellcarcinoma AT xuliyan novelclinicalsixflavoproteingenesignaturepredictsprognosisinesophagealsquamouscellcarcinoma AT lienmin novelclinicalsixflavoproteingenesignaturepredictsprognosisinesophagealsquamouscellcarcinoma |