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
  • [11] The expression of ETAR in liver cirrhosis and liver cancer
    Deng, Juhong
    Huang, Yu
    Tao, Ran
    Fan, Xiangxue
    Zhang, Hongyue
    Kong, Hongyan
    Song, Qiqing
    Huang, Jiaquan
    CANCER BIOLOGY & THERAPY, 2017, 18 (09) : 723 - 729
  • [12] Identification of a minimum number of genes to predict triple-negative breast cancer subgroups from gene expression profiles
    Akhouayri, Laila
    Ostano, Paola
    Mello-Grand, Maurizia
    Gregnanin, Ilaria
    Crivelli, Francesca
    Laurora, Sara
    Liscia, Daniele
    Leone, Francesco
    Santoro, Angela
    Mule, Antonino
    Guarino, Donatella
    Maggiore, Claudia
    Carlino, Angela
    Magno, Stefano
    Scatolini, Maria
    Di Leone, Alba
    Masetti, Riccardo
    Chiorino, Giovanna
    HUMAN GENOMICS, 2022, 16 (01)
  • [13] Gene expression profiles reveal significant differences between rat liver cancer and liver regeneration
    Wang, Gaiping
    Xu, Cunshuan
    Zhi, Jia
    Hao, Yunpeng
    Zhang, Lianxing
    Chang, Cuifang
    GENE, 2012, 504 (01) : 41 - 52
  • [14] Identification of the molecular mechanisms underlying dilated cardiomyopathy via bioinformatic analysis of gene expression profiles
    Zhang, Hu
    Yu, Zhuo
    He, Jianchao
    Hua, Baotong
    Zhang, Guiming
    EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2017, 13 (01) : 273 - 279
  • [15] Computational identification of microRNAs and their targets in liver cirrhosis
    Du, Hongbo
    Yu, Hao
    Yang, Yuying
    Song, Yuanyuan
    Wang, Fei
    Li, Shangheng
    Jiang, Yuyong
    ONCOLOGY LETTERS, 2017, 14 (06) : 7691 - 7698
  • [16] Liver cirrhosis: molecular mechanisms and therapeutic interventions
    Dong, Zihe
    Wang, Yeying
    Jin, Weilin
    MEDCOMM, 2024, 5 (10):
  • [17] Gene expression profiles associated with inflammation, fibrosis, and cholestasis in mouse liver after griseofulvin
    Gant, TW
    Baus, PR
    Clothier, B
    Riley, J
    Davies, R
    Judah, DJ
    Edwards, RE
    George, E
    Greaves, P
    Smith, AG
    ENVIRONMENTAL HEALTH PERSPECTIVES, 2003, 111 (06) : 847 - 853
  • [18] Gene expression profiles in liver regeneration with oval cell induction
    Arai, M
    Yokosuka, O
    Fukai, K
    Imazeki, F
    Chiba, T
    Sumi, H
    Kato, M
    Takiguchi, M
    Saisho, H
    Muramatsu, M
    Seki, N
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 317 (02) : 370 - 376
  • [19] Gene microarray analysis of expression profiles in liver ischemia and reperfusion
    Zheng, Xiaoyang
    Zhou, Huaqiang
    Qiu, Zeting
    Gao, Shaowei
    Wang, Zhongxing
    Xiao, Liangcan
    MOLECULAR MEDICINE REPORTS, 2017, 16 (03) : 3299 - 3307
  • [20] Identification of gene expression profiles correlated to tumor progression in a preclinical model of colon carcinogenesis
    Bousserouel, Souad
    Kauntz, Henriette
    Gosse, Francine
    Bouhadjar, Mourad
    Soler, Luc
    Marescaux, Jacques
    Raul, Francis
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2010, 36 (06) : 1485 - 1490