Development of a Four-mRNA Expression-Based Prognostic Signature for Cutaneous Melanoma

We aim to find a biomarker that can effectively predict the prognosis of patients with cutaneous melanoma (CM). The RNA sequencing data of CM was downloaded from The Cancer Genome Atlas (TCGA) database and randomly divided into training group and test group. Survival statistical analysis and machine...

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Main Authors: Haiya Bai, Youliang Wang, Huimin Liu, Junyang Lu
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-07-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2021.680617/full
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spelling doaj-6b2a7c6e11134e4fb960dd66944e3db22021-07-15T15:57:22ZengFrontiers Media S.A.Frontiers in Genetics1664-80212021-07-011210.3389/fgene.2021.680617680617Development of a Four-mRNA Expression-Based Prognostic Signature for Cutaneous MelanomaHaiya Bai0Youliang Wang1Huimin Liu2Junyang Lu3Department of Female Plastic Surgery, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, ChinaDepartment of Pediatric Surgery, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, ChinaDepartment of Female Plastic Surgery, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, ChinaDepartment of Female Plastic Surgery, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, ChinaWe aim to find a biomarker that can effectively predict the prognosis of patients with cutaneous melanoma (CM). The RNA sequencing data of CM was downloaded from The Cancer Genome Atlas (TCGA) database and randomly divided into training group and test group. Survival statistical analysis and machine-learning approaches were performed on the RNA sequencing data of CM to develop a prognostic signature. Using univariable Cox proportional hazards regression, random survival forest algorithm, and receiver operating characteristic (ROC) in the training group, the four-mRNA signature including CD276, UQCRFS1, HAPLN3, and PIP4P1 was screened out. The four-mRNA signature could divide patients into low-risk and high-risk groups with different survival outcomes (log-rank p < 0.001). The predictive efficacy of the four-mRNA signature was confirmed in the test group, the whole TCGA group, and the independent GSE65904 (log-rank p < 0.05). The independence of the four-mRNA signature in prognostic prediction was demonstrated by multivariate Cox analysis. ROC and timeROC analyses showed that the efficiency of the signature in survival prediction was better than other clinical variables such as melanoma Clark level and tumor stage. This study highlights that the four-mRNA model could be used as a prognostic signature for CM patients with potential clinical application value.https://www.frontiersin.org/articles/10.3389/fgene.2021.680617/fullcutaneous melanomaprognostic signaturerandom survival forestMRNA expression datamachine learning
collection DOAJ
language English
format Article
sources DOAJ
author Haiya Bai
Youliang Wang
Huimin Liu
Junyang Lu
spellingShingle Haiya Bai
Youliang Wang
Huimin Liu
Junyang Lu
Development of a Four-mRNA Expression-Based Prognostic Signature for Cutaneous Melanoma
Frontiers in Genetics
cutaneous melanoma
prognostic signature
random survival forest
MRNA expression data
machine learning
author_facet Haiya Bai
Youliang Wang
Huimin Liu
Junyang Lu
author_sort Haiya Bai
title Development of a Four-mRNA Expression-Based Prognostic Signature for Cutaneous Melanoma
title_short Development of a Four-mRNA Expression-Based Prognostic Signature for Cutaneous Melanoma
title_full Development of a Four-mRNA Expression-Based Prognostic Signature for Cutaneous Melanoma
title_fullStr Development of a Four-mRNA Expression-Based Prognostic Signature for Cutaneous Melanoma
title_full_unstemmed Development of a Four-mRNA Expression-Based Prognostic Signature for Cutaneous Melanoma
title_sort development of a four-mrna expression-based prognostic signature for cutaneous melanoma
publisher Frontiers Media S.A.
series Frontiers in Genetics
issn 1664-8021
publishDate 2021-07-01
description We aim to find a biomarker that can effectively predict the prognosis of patients with cutaneous melanoma (CM). The RNA sequencing data of CM was downloaded from The Cancer Genome Atlas (TCGA) database and randomly divided into training group and test group. Survival statistical analysis and machine-learning approaches were performed on the RNA sequencing data of CM to develop a prognostic signature. Using univariable Cox proportional hazards regression, random survival forest algorithm, and receiver operating characteristic (ROC) in the training group, the four-mRNA signature including CD276, UQCRFS1, HAPLN3, and PIP4P1 was screened out. The four-mRNA signature could divide patients into low-risk and high-risk groups with different survival outcomes (log-rank p < 0.001). The predictive efficacy of the four-mRNA signature was confirmed in the test group, the whole TCGA group, and the independent GSE65904 (log-rank p < 0.05). The independence of the four-mRNA signature in prognostic prediction was demonstrated by multivariate Cox analysis. ROC and timeROC analyses showed that the efficiency of the signature in survival prediction was better than other clinical variables such as melanoma Clark level and tumor stage. This study highlights that the four-mRNA model could be used as a prognostic signature for CM patients with potential clinical application value.
topic cutaneous melanoma
prognostic signature
random survival forest
MRNA expression data
machine learning
url https://www.frontiersin.org/articles/10.3389/fgene.2021.680617/full
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AT youliangwang developmentofafourmrnaexpressionbasedprognosticsignatureforcutaneousmelanoma
AT huiminliu developmentofafourmrnaexpressionbasedprognosticsignatureforcutaneousmelanoma
AT junyanglu developmentofafourmrnaexpressionbasedprognosticsignatureforcutaneousmelanoma
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