Cargando…

Development of an oncogenic dedifferentiation SOX signature with prognostic significance in hepatocellular carcinoma

BACKGROUND: Gradual loss of terminal differentiation markers and gain of stem cell-like properties is a major hall mark of cancer malignant progression. The stem cell pluripotent transcriptional factor SOX family play critical roles in governing tumor plasticity and lineage specification. This study...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Mei-Mei, Tang, Yun-Qiang, Gong, Yuan-Feng, Cheng, Wei, Li, Hao-Long, Kong, Fan-En, Zhu, Wen-Jie, Liu, Shan-Shan, Huang, Li, Guan, Xin-Yuan, Ma, Ning-Fang, Liu, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6714407/
https://www.ncbi.nlm.nih.gov/pubmed/31462277
http://dx.doi.org/10.1186/s12885-019-6041-2
_version_ 1783447061873557504
author Li, Mei-Mei
Tang, Yun-Qiang
Gong, Yuan-Feng
Cheng, Wei
Li, Hao-Long
Kong, Fan-En
Zhu, Wen-Jie
Liu, Shan-Shan
Huang, Li
Guan, Xin-Yuan
Ma, Ning-Fang
Liu, Ming
author_facet Li, Mei-Mei
Tang, Yun-Qiang
Gong, Yuan-Feng
Cheng, Wei
Li, Hao-Long
Kong, Fan-En
Zhu, Wen-Jie
Liu, Shan-Shan
Huang, Li
Guan, Xin-Yuan
Ma, Ning-Fang
Liu, Ming
author_sort Li, Mei-Mei
collection PubMed
description BACKGROUND: Gradual loss of terminal differentiation markers and gain of stem cell-like properties is a major hall mark of cancer malignant progression. The stem cell pluripotent transcriptional factor SOX family play critical roles in governing tumor plasticity and lineage specification. This study aims to establish a novel SOX signature to monitor the extent of tumor dedifferentiation and predict prognostic significance in hepatocellular carcinoma (HCC). METHODS: The RNA-seq data from The Cancer Genome Atlas (TCGA) LIHC project were chronologically divided into the training (n = 188) and testing cohort (n = 189). LIRI-JP project from International Cancer Genome Consortium (ICGC) data portal was used as an independent validation cohort (n = 232). Kaplan-Meier and multivariable Cox analyses were used to examine the clinical significance and prognostic value of the signature genes. RESULTS: The SOX gene family members were found to be aberrantly expressed in clinical HCC patients. A five-gene SOX signature with prognostic value was established in the training cohort. The SOX signature genes were found to be closely associated with tumor grade and tumor stage. Liver cancer dedifferentiation markers (AFP, CD133, EPCAM, and KRT19) were found to be progressively increased while hepatocyte terminal differentiation markers (ALB, G6PC, CYP3A4, and HNF4A) were progressively decreased from HCC patients with low SOX signature scores to patients with high SOX signature scores. Kaplan-Meier survival analysis further indicated that the newly established SOX signature could robustly predict patient overall survival in both training, testing, and independent validation cohort. CONCLUSIONS: An oncogenic dedifferentiation SOX signature presents a great potential in predicting prognostic significance in HCC, and might provide novel biomarkers for precision oncology further in the clinic. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-019-6041-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6714407
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-67144072019-09-04 Development of an oncogenic dedifferentiation SOX signature with prognostic significance in hepatocellular carcinoma Li, Mei-Mei Tang, Yun-Qiang Gong, Yuan-Feng Cheng, Wei Li, Hao-Long Kong, Fan-En Zhu, Wen-Jie Liu, Shan-Shan Huang, Li Guan, Xin-Yuan Ma, Ning-Fang Liu, Ming BMC Cancer Research Article BACKGROUND: Gradual loss of terminal differentiation markers and gain of stem cell-like properties is a major hall mark of cancer malignant progression. The stem cell pluripotent transcriptional factor SOX family play critical roles in governing tumor plasticity and lineage specification. This study aims to establish a novel SOX signature to monitor the extent of tumor dedifferentiation and predict prognostic significance in hepatocellular carcinoma (HCC). METHODS: The RNA-seq data from The Cancer Genome Atlas (TCGA) LIHC project were chronologically divided into the training (n = 188) and testing cohort (n = 189). LIRI-JP project from International Cancer Genome Consortium (ICGC) data portal was used as an independent validation cohort (n = 232). Kaplan-Meier and multivariable Cox analyses were used to examine the clinical significance and prognostic value of the signature genes. RESULTS: The SOX gene family members were found to be aberrantly expressed in clinical HCC patients. A five-gene SOX signature with prognostic value was established in the training cohort. The SOX signature genes were found to be closely associated with tumor grade and tumor stage. Liver cancer dedifferentiation markers (AFP, CD133, EPCAM, and KRT19) were found to be progressively increased while hepatocyte terminal differentiation markers (ALB, G6PC, CYP3A4, and HNF4A) were progressively decreased from HCC patients with low SOX signature scores to patients with high SOX signature scores. Kaplan-Meier survival analysis further indicated that the newly established SOX signature could robustly predict patient overall survival in both training, testing, and independent validation cohort. CONCLUSIONS: An oncogenic dedifferentiation SOX signature presents a great potential in predicting prognostic significance in HCC, and might provide novel biomarkers for precision oncology further in the clinic. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-019-6041-2) contains supplementary material, which is available to authorized users. BioMed Central 2019-08-28 /pmc/articles/PMC6714407/ /pubmed/31462277 http://dx.doi.org/10.1186/s12885-019-6041-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Li, Mei-Mei
Tang, Yun-Qiang
Gong, Yuan-Feng
Cheng, Wei
Li, Hao-Long
Kong, Fan-En
Zhu, Wen-Jie
Liu, Shan-Shan
Huang, Li
Guan, Xin-Yuan
Ma, Ning-Fang
Liu, Ming
Development of an oncogenic dedifferentiation SOX signature with prognostic significance in hepatocellular carcinoma
title Development of an oncogenic dedifferentiation SOX signature with prognostic significance in hepatocellular carcinoma
title_full Development of an oncogenic dedifferentiation SOX signature with prognostic significance in hepatocellular carcinoma
title_fullStr Development of an oncogenic dedifferentiation SOX signature with prognostic significance in hepatocellular carcinoma
title_full_unstemmed Development of an oncogenic dedifferentiation SOX signature with prognostic significance in hepatocellular carcinoma
title_short Development of an oncogenic dedifferentiation SOX signature with prognostic significance in hepatocellular carcinoma
title_sort development of an oncogenic dedifferentiation sox signature with prognostic significance in hepatocellular carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6714407/
https://www.ncbi.nlm.nih.gov/pubmed/31462277
http://dx.doi.org/10.1186/s12885-019-6041-2
work_keys_str_mv AT limeimei developmentofanoncogenicdedifferentiationsoxsignaturewithprognosticsignificanceinhepatocellularcarcinoma
AT tangyunqiang developmentofanoncogenicdedifferentiationsoxsignaturewithprognosticsignificanceinhepatocellularcarcinoma
AT gongyuanfeng developmentofanoncogenicdedifferentiationsoxsignaturewithprognosticsignificanceinhepatocellularcarcinoma
AT chengwei developmentofanoncogenicdedifferentiationsoxsignaturewithprognosticsignificanceinhepatocellularcarcinoma
AT lihaolong developmentofanoncogenicdedifferentiationsoxsignaturewithprognosticsignificanceinhepatocellularcarcinoma
AT kongfanen developmentofanoncogenicdedifferentiationsoxsignaturewithprognosticsignificanceinhepatocellularcarcinoma
AT zhuwenjie developmentofanoncogenicdedifferentiationsoxsignaturewithprognosticsignificanceinhepatocellularcarcinoma
AT liushanshan developmentofanoncogenicdedifferentiationsoxsignaturewithprognosticsignificanceinhepatocellularcarcinoma
AT huangli developmentofanoncogenicdedifferentiationsoxsignaturewithprognosticsignificanceinhepatocellularcarcinoma
AT guanxinyuan developmentofanoncogenicdedifferentiationsoxsignaturewithprognosticsignificanceinhepatocellularcarcinoma
AT maningfang developmentofanoncogenicdedifferentiationsoxsignaturewithprognosticsignificanceinhepatocellularcarcinoma
AT liuming developmentofanoncogenicdedifferentiationsoxsignaturewithprognosticsignificanceinhepatocellularcarcinoma