Cargando…

Co-expression analysis of differentially expressed genes in hepatitis C virus-induced hepatocellular carcinoma

The aim of the current study was to investigate the molecular mechanisms underlying hepatitis C virus (HCV)-induced hepatocellular carcinoma (HCC) using the expression profiles of HCV-infected Huh7 cells at different time points. The differentially expressed genes (DEGs) were identified with the Sam...

Descripción completa

Detalles Bibliográficos
Autores principales: SONG, QINGFENG, ZHAO, CHANG, OU, SHENGQIU, MENG, ZHIBIN, KANG, PING, FAN, LIWEI, QI, FENG, MA, YILONG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237098/
https://www.ncbi.nlm.nih.gov/pubmed/25339452
http://dx.doi.org/10.3892/mmr.2014.2695
_version_ 1782345292645924864
author SONG, QINGFENG
ZHAO, CHANG
OU, SHENGQIU
MENG, ZHIBIN
KANG, PING
FAN, LIWEI
QI, FENG
MA, YILONG
author_facet SONG, QINGFENG
ZHAO, CHANG
OU, SHENGQIU
MENG, ZHIBIN
KANG, PING
FAN, LIWEI
QI, FENG
MA, YILONG
author_sort SONG, QINGFENG
collection PubMed
description The aim of the current study was to investigate the molecular mechanisms underlying hepatitis C virus (HCV)-induced hepatocellular carcinoma (HCC) using the expression profiles of HCV-infected Huh7 cells at different time points. The differentially expressed genes (DEGs) were identified with the Samr package in R software once the data were normalized. Functional and pathway enrichment analysis of the identified DEGs was also performed. Subsequently, MCODE in Cytoscape software was applied to conduct module analysis of the constructed co-expression networks. A total of 1,100 DEGs were identified between the HCV-infected and control samples at 12, 18, 24 and 48 h post-infection. DEGs at 24 and 48 h were involved in the same signaling pathways and biological processes, including sterol biosynthetic processes and tRNA amino-acylation. There were 22 time series genes which were clustered into 3 expression patterns, and the demarcation point of the 2 expression patterns that 401 overlapping DEGs at 24 and 48 h clustered into was 24 h post-infection. tRNA synthesis-related biological processes emerged at 24 and 48 h. Replication and assembly of HCV in HCV-infected Huh7 cells occurred mainly at 24 h post-infection. In view of this, the screened time series genes have the potential to become candidate target molecules for monitoring, diagnosing and treating HCV-induced HCC.
format Online
Article
Text
id pubmed-4237098
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-42370982014-11-19 Co-expression analysis of differentially expressed genes in hepatitis C virus-induced hepatocellular carcinoma SONG, QINGFENG ZHAO, CHANG OU, SHENGQIU MENG, ZHIBIN KANG, PING FAN, LIWEI QI, FENG MA, YILONG Mol Med Rep Articles The aim of the current study was to investigate the molecular mechanisms underlying hepatitis C virus (HCV)-induced hepatocellular carcinoma (HCC) using the expression profiles of HCV-infected Huh7 cells at different time points. The differentially expressed genes (DEGs) were identified with the Samr package in R software once the data were normalized. Functional and pathway enrichment analysis of the identified DEGs was also performed. Subsequently, MCODE in Cytoscape software was applied to conduct module analysis of the constructed co-expression networks. A total of 1,100 DEGs were identified between the HCV-infected and control samples at 12, 18, 24 and 48 h post-infection. DEGs at 24 and 48 h were involved in the same signaling pathways and biological processes, including sterol biosynthetic processes and tRNA amino-acylation. There were 22 time series genes which were clustered into 3 expression patterns, and the demarcation point of the 2 expression patterns that 401 overlapping DEGs at 24 and 48 h clustered into was 24 h post-infection. tRNA synthesis-related biological processes emerged at 24 and 48 h. Replication and assembly of HCV in HCV-infected Huh7 cells occurred mainly at 24 h post-infection. In view of this, the screened time series genes have the potential to become candidate target molecules for monitoring, diagnosing and treating HCV-induced HCC. D.A. Spandidos 2015-01 2014-10-17 /pmc/articles/PMC4237098/ /pubmed/25339452 http://dx.doi.org/10.3892/mmr.2014.2695 Text en Copyright © 2015, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
SONG, QINGFENG
ZHAO, CHANG
OU, SHENGQIU
MENG, ZHIBIN
KANG, PING
FAN, LIWEI
QI, FENG
MA, YILONG
Co-expression analysis of differentially expressed genes in hepatitis C virus-induced hepatocellular carcinoma
title Co-expression analysis of differentially expressed genes in hepatitis C virus-induced hepatocellular carcinoma
title_full Co-expression analysis of differentially expressed genes in hepatitis C virus-induced hepatocellular carcinoma
title_fullStr Co-expression analysis of differentially expressed genes in hepatitis C virus-induced hepatocellular carcinoma
title_full_unstemmed Co-expression analysis of differentially expressed genes in hepatitis C virus-induced hepatocellular carcinoma
title_short Co-expression analysis of differentially expressed genes in hepatitis C virus-induced hepatocellular carcinoma
title_sort co-expression analysis of differentially expressed genes in hepatitis c virus-induced hepatocellular carcinoma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237098/
https://www.ncbi.nlm.nih.gov/pubmed/25339452
http://dx.doi.org/10.3892/mmr.2014.2695
work_keys_str_mv AT songqingfeng coexpressionanalysisofdifferentiallyexpressedgenesinhepatitiscvirusinducedhepatocellularcarcinoma
AT zhaochang coexpressionanalysisofdifferentiallyexpressedgenesinhepatitiscvirusinducedhepatocellularcarcinoma
AT oushengqiu coexpressionanalysisofdifferentiallyexpressedgenesinhepatitiscvirusinducedhepatocellularcarcinoma
AT mengzhibin coexpressionanalysisofdifferentiallyexpressedgenesinhepatitiscvirusinducedhepatocellularcarcinoma
AT kangping coexpressionanalysisofdifferentiallyexpressedgenesinhepatitiscvirusinducedhepatocellularcarcinoma
AT fanliwei coexpressionanalysisofdifferentiallyexpressedgenesinhepatitiscvirusinducedhepatocellularcarcinoma
AT qifeng coexpressionanalysisofdifferentiallyexpressedgenesinhepatitiscvirusinducedhepatocellularcarcinoma
AT mayilong coexpressionanalysisofdifferentiallyexpressedgenesinhepatitiscvirusinducedhepatocellularcarcinoma