Comparative gene and protein expression analyses of a panel of cytokines in acute and chronic drug-induced liver injury in rats

被引:10
作者
Hanafusa, Hiroyuki [1 ]
Morikawa, Yuji [1 ,2 ]
Uehara, Takeki [1 ,2 ]
Kaneto, Masako [1 ]
Ono, Atsushi [2 ]
Yamada, Hiroshi [2 ]
Ohno, Yasuo [3 ]
Urushidani, Tetsuro [2 ,4 ]
机构
[1] Shionogi & Co Ltd, Dev Res Labs, Toyonaka, Osaka 5610825, Japan
[2] Natl Inst Biomed Innovat, Toxicogen Informat Project, Ibaraki, Osaka, Japan
[3] Natl Inst Hlth Sci, Setagaya Ku, Tokyo, Japan
[4] Doshisha Womens Coll Liberal Arts, Fac Pharmaceut Sci, Dept Pathophysiol, Kyoto, Japan
关键词
Cytokines; Toxicogenomics; mRNA; Protein; Hepatotoxicity; Biomarkers; MESSENGER-RNA; HEPATOTOXICITY; MECHANISMS; QUANTIFICATION; INFLAMMATION; RECRUITMENT; RELEVANCE; ARTHRITIS; TOXICITY;
D O I
10.1016/j.tox.2014.07.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Drug-induced liver injury (DILI) is a significant safety issue associated with medication use, and is the major cause of failures in drug development and withdrawal in post marketing. Cytokines are signaling molecules produced and secreted by immune cells and play crucial roles in the progression of DILI. Although there are numerous reports of cytokine changes in several DILI models, a comprehensive analysis of cytokine expression changes in rat liver injury induced by various compounds has, to the best of our knowledge, not been performed. In the past several years, we have built a public, free, large-scale toxicogenomics database, called Open TG-GATEs, containing microarray data and toxicity data of the liver of rats treated with various hepatotoxic compounds. In this study, we measured the protein expression levels of a panel of 24 cytokines in frozen liver of rats treated with a total of 20 compounds, obtained in the original study that formed the basis of the Open TG-GATEs database and analyzed protein expression profiles combined with mRNA expression profiles to investigate the correlation between mRNA and protein expression levels. As a result, we demonstrated significant correlations between mRNA and protein expression changes for interleukin (IL)-1 beta, IL-1 alpha, monocyte chemo-attractant protein (MCP)-1/CC-chemokine ligand (Ccl)2, vascular endothelial growth factor A (VEGF-A), and regulated upon activation normal T cell expressed and secreted (RANTES)/Ccl5 in several different types of DILI. We also demonstrated that IL-1 beta protein and MCP-1/Ccl2 mRNA were commonly up-regulated in the liver of rats treated with different classes of hepatotoxicants and exhibited the highest accuracy in the detection of hepatotoxicity. The results also demonstrate that hepatic mRNA changes do not always correlate with protein changes of cytokines in the liver. This is the first study to provide a comprehensive analysis of mRNA protein correlations of factors involved in various types of DILI, as well as additional insights into the importance of understanding complex cytokine expression changes in assessing DILI. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:43 / 54
页数:12
相关论文
共 33 条
[1]   The Evolution of Bioinformatics in Toxicology: Advancing Toxicogenomics [J].
Afshari, Cynthia A. ;
Hamadeh, Hisham K. ;
Bushel, Pierre R. .
TOXICOLOGICAL SCIENCES, 2011, 120 :S225-S237
[2]   Induction of chemokines and cytokines before neutrophils and macrophage recruitment in different regions of rat liver after TAA administration [J].
Amanzada, Ahmad ;
Moriconi, Federico ;
Mansuroglu, Tuemen ;
Cameron, Silke ;
Ramadori, Giuliano ;
Malik, Ihtzaz A. .
LABORATORY INVESTIGATION, 2014, 94 (02) :235-247
[3]  
[Anonymous], 1996, J COMPUT GRAPH STAT
[4]   An In Vitro Assay to Assess Transporter-Based Cholestatic Hepatotoxicity Using Sandwich-Cultured Rat Hepatocytes [J].
Ansede, John H. ;
Smith, William R. ;
Perry, Cassandra H. ;
St Claire, Robert L., III ;
Brouwer, Kenneth R. .
DRUG METABOLISM AND DISPOSITION, 2010, 38 (02) :276-280
[5]   ROLE OF PROINFLAMMATORY CYTOKINES IN ACETAMINOPHEN HEPATOTOXICITY [J].
BLAZKA, ME ;
WILMER, JL ;
HOLLADAY, SD ;
WILSON, RE ;
LUSTER, MI .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1995, 133 (01) :43-52
[6]   Immune Response to Extracellular Matrix Collagen in Chronic Hepatitis C-Induced Liver Fibrosis [J].
Borg, Brian B. ;
Seetharam, Anil ;
Subramanian, Vijay ;
Basha, Haseeb Ilias ;
Lisker-Melman, Mauricio ;
Korenblat, Kevin ;
Anderson, Christopher D. ;
Shenoy, Surendra ;
Chapman, William C. ;
Crippin, Jeffrey S. ;
Mohanakumar, Thalachallour .
LIVER TRANSPLANTATION, 2011, 17 (07) :814-823
[7]  
Cui YX, 2010, PHARMACOGENOMICS, V11, P573, DOI [10.2217/pgs.10.37, 10.2217/PGS.10.37]
[8]   Monocyte Chemoattractant Protein-1 (MCP-1): An Overview [J].
Deshmane, Satish L. ;
Kremlev, Sergey ;
Amini, Shohreh ;
Sawaya, Bassel E. .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2009, 29 (06) :313-326
[9]   Mechanisms of Drug Toxicity and Relevance to Pharmaceutical Development [J].
Guengerich, F. Peter .
DRUG METABOLISM AND PHARMACOKINETICS, 2011, 26 (01) :3-14
[10]   Increase in covalent binding of 5-hydroxydiclofenac to hepatic tissues in rats co-treated with lipopolysaccharide and diclofenac: involvement in the onset of diclofenac-induced idiosyncratic hepatotoxicity [J].
Kishida, Tomoyuki ;
Onozato, Tomoya ;
Kanazawa, Toru ;
Tanaka, Satoru ;
Kuroda, Junji .
JOURNAL OF TOXICOLOGICAL SCIENCES, 2012, 37 (06) :1143-1156