Identification of Molecular Subgroups in Liver Cirrhosis by Gene Expression Profiles

被引:0
作者
Zhang, Ying-Xue [1 ]
Sun, Feng-Xia [1 ]
Li, Xiao-Ling [1 ]
Liu, Qing-Hua [2 ]
Chen, Zi-Meng [1 ]
Guo, Yu-Fei [1 ]
机构
[1] Capital Med Univ, Dept Infect, Beijing Hosp Tradit Chinese Med, Beijing 100010, Peoples R China
[2] Beijing Univ Chinese Med, Beijing, Peoples R China
关键词
Liver Cirrhosis; Gene Expression Profile; Classification of Subgroups; Weighted Gene Coexpression Network Analysis Module; FIBROSIS; SUBTYPES; INFLAMMATION; DISCOVERY; NETWORK; CELLS;
D O I
10.5812/hepatmon.118535
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Liver cirrhosis is characterized by high mortality, bringing a serious health and economic burden to the world. The clinical manifestations of liver cirrhosis are complex and heterogeneous. According to subgroup characteristics, identifying cirrhosis has become a challenge. Objectives: The purpose of this study was to evaluate the difference between different subgroups of cirrhosis. The ultimate goal of research on these different phenotypes was to discover groups of patients with unique treatment characteristics, and formulate targeted treatment plans that improve the prognosis of the disease and improve the patients' quality of life. Methods: We obtained the relevant gene chip by searching the gene expression omnibus (GEO) database. According to the gene expression profile, 79 patients with liver cirrhosis were divided into four subgroups, which showed different expression patterns. Therefore, we used weighted gene coexpression network analysis (WGCNA) to find differences between subgroups. Results: The characteristics of the WGCNA module indicated that subjects in subgroup I might exhibit inflammatory characteristics; subjects in subgroup II might exhibit metabolically active characteristics; arrhythmogenic right ventricular cardiomyopathy and neuroactive ligand-receptive somatic interaction pathways were significantly enriched in subgroup IV. We did not find a significantly upregulated pathway in the third subgroup. Conclusions: In this study, a new type of clinical phenotype classification of liver cirrhosis was derived by consensus clustering. This study found that patients in different subgroups may have unique gene expression patterns. This new classification method helps researchers explore new treatment strategies for cirrhosis based on clinical phenotypic characteristics.
引用
收藏
页数:11
相关论文
共 50 条
[21]   Identification of proteasome inhibitors using analysis of gene expression profiles [J].
Mofers, Arjan ;
Selvaraju, Karthik ;
Gubat, Johannes ;
D 'Arcy, Padraig ;
Linder, Stig .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2020, 889
[22]   Identification of Gene Expression Profiles by Microarray and Confirmation of Gene Expression by RT-PCR during Osteoblastic Differentiation by BMP-2 [J].
Lee, Juyoun ;
Chung, Jin ;
Kim, Ji Hyun ;
Jeong, Myung Ho ;
Yoon, Taek Rim ;
Kim, Hyung Keun .
TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2010, 7 (02) :155-162
[23]   Gene therapy for liver cirrhosis [J].
Fujimoto, J .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2000, 15 :D33-D36
[24]   Genome-wide gene expression profiles of thyroid carcinoma: Identification of molecular targets for treatment of thyroid carcinoma [J].
Nikolova, Dragomira Nikolaeva ;
Zembutsu, Hitoshi ;
Sechanov, Tanio ;
Vidinov, Kalin ;
Kee, Low Siew ;
Ivanova, Radina ;
Becheva, Elitza ;
Kocova, Miriana ;
Toncheva, Draga ;
Nakamura, Yusuke .
ONCOLOGY REPORTS, 2008, 20 (01) :105-121
[25]   Effects of green tea on ACE gene expression in rat liver in CCl4-induced cirrhosis [J].
Shahid, Syed Muhammad ;
Shaikh, Rozeena ;
Shamim, Sana ;
Ismail, Muhammad ;
Mahboob, Tabassum .
TURKISH JOURNAL OF MEDICAL SCIENCES, 2013, 43 (04) :586-591
[26]   Age and Diet Affect Gene Expression Profiles in Canine Liver Tissue [J].
Kil, Dong Yong ;
Boler, Brittany M. Vester ;
Apanavicius, Carolyn J. ;
Schook, Lawrence B. ;
Swanson, Kelly S. .
PLOS ONE, 2010, 5 (10)
[27]   Identification of biomarkers that distinguish chemical contaminants based on gene expression profiles [J].
Wei, Xiaomou ;
Ai, Junmei ;
Deng, Youping ;
Guan, Xin ;
Johnson, David R. ;
Ang, Choo Y. ;
Zhang, Chaoyang ;
Perkins, Edward J. .
BMC GENOMICS, 2014, 15
[28]   Identifying Cancer Patient Subgroups by Finding Co-Modules From the Driver Mutation Profiles and Downstream Gene Expression Profiles [J].
Song, Junrong ;
Peng, Wei ;
Wang, Feng .
IEEE-ACM TRANSACTIONS ON COMPUTATIONAL BIOLOGY AND BIOINFORMATICS, 2022, 19 (05) :2863-2872
[29]   Liver stiffness correlates with serum osteopontin and tafazzin expression in human liver cirrhosis [J].
Khajehahmadi, Zohreh ;
Mohagheghi, Sina ;
Nikeghbalian, Saman ;
Geramizadeh, Bita ;
Khodadadi, Iraj ;
Karimi, Jamshid ;
Tavilani, Heidar .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 2020, 1465 (01) :117-131
[30]   Molecular pathogenesis and clinical consequences of iron overload in liver cirrhosis [J].
Katarzyna Sikorska ;
Agnieszka Bernat ;
Anna Wrblewska .
Hepatobiliary&PancreaticDiseasesInternational, 2016, 15 (05) :461-479