Epigenetic modification in liver fibrosis: Promising therapeutic direction with significant challenges ahead

被引:16
作者
Liu, Runping [1 ]
Li, Yajing [2 ]
Zheng, Qi [1 ]
Ding, Mingning [2 ]
Zhou, Huiping [3 ]
Li, Xiaojiaoyang [2 ]
机构
[1] Beijing Univ Chinese Med, Sch Chinese Mat Med, Beijing 102400, Peoples R China
[2] Beijing Univ Chinese Med, Sch Life Sci, Beijing 102400, Peoples R China
[3] Virginia Commonwealth Univ, Dept Microbiol & Immunol, Richmond, VA 22460 USA
基金
美国国家卫生研究院;
关键词
Liver fibrosis; Epigenetics regulation; DNA methylation; Histone acetylation; Histone methylation; mRNA methylation; Non-coding RNA; Drug development; HEPATIC STELLATE CELLS; HISTONE DEACETYLASE INHIBITOR; GROWTH-FACTOR-BETA; TO-MESENCHYMAL TRANSITION; ACTIVATED RECEPTOR-GAMMA; LONG NONCODING RNA; DNA METHYLATION; TGF-BETA; TISSUE FIBROSIS; UP-REGULATION;
D O I
10.1016/j.apsb.2023.10.023
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Liver fibrosis, characterized by scar tissue formation, can ultimately result in liver failure. It's a major cause of morbidity and mortality globally, often associated with chronic liver diseases like hepatitis or alcoholic and non-alcoholic fatty liver diseases. However, current treatment options are limited, highlighting the urgent need for the development of new therapies. As a reversible regulatory mechanism, epigenetic modification is implicated in many biological processes, including liver fibrosis. Exploring the epigenetic mechanisms involved in liver fibrosis could provide valuable insights into developing new treatments for chronic liver diseases, although the current evidence is still controversial. This review provides a comprehensive summary of the regulatory mechanisms and critical targets of epigenetic modifications, including DNA methylation, histone modification, and RNA modification, in liver fibrotic diseases. The potential cooperation of different epigenetic modifications in promoting fibrogenesis was also highlighted. Finally, available agonists or inhibitors regulating these epigenetic mechanisms and their potential application in preventing liver fibrosis were discussed. In summary, elucidating specific druggable epigenetic targets and developing more selective and specific candidate medicines may represent a promising approach with bright prospects for the treatment of chronic liver diseases.
引用
收藏
页码:1009 / 1029
页数:21
相关论文
共 181 条
[1]   Sildenafil protects against bile duct ligation induced hepatic fibrosis in rats: Potential role for silent information regulator 1 (SIRT1) [J].
Abd El Motteleb, Dalia M. ;
Ibrahim, Islam A. A. E. -H. ;
Elshazly, Shimaa M. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2017, 335 :64-71
[2]   Valproate ameliorates thioacetamide-induced fibrosis by hepatic stellate cell inactivation [J].
Aher, J. S. ;
Khan, S. ;
Jain, S. ;
Tikoo, K. ;
Jena, G. .
HUMAN & EXPERIMENTAL TOXICOLOGY, 2015, 34 (01) :44-55
[3]   MicroRNA-based diagnostic tools for advanced fibrosis and cirrhosis in patients with chronic hepatitis B and C [J].
Appourchaux, Kevin ;
Dokmak, Safi ;
Resche-Rigon, Matthieu ;
Treton, Xavier ;
Lapalus, Martine ;
Gattolliat, Charles-Henry ;
Porchet, Emmanuelle ;
Martinot-Peignoux, Michelle ;
Boyer, Nathalie ;
Vidaud, Michel ;
Bedossa, Pierre ;
Marcellin, Patrick ;
Bieche, Ivan ;
Estrabaud, Emilie ;
Asselah, Tarik .
SCIENTIFIC REPORTS, 2016, 6
[4]   Thiazolidinediones for the Treatment in NASH Sustained Benefit After Drug Discontinuation? [J].
Argo, Curtis K. ;
Iezzoni, Julia C. ;
Al-Osaimi, Abdullah M. S. ;
Caldwell, Stephen H. .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 2009, 43 (06) :565-568
[5]   Inhibition of SIRT2 suppresses hepatic fibrosis [J].
Arteaga, Maribel ;
Shang, Na ;
Ding, Xianzhong ;
Yong, Sherri ;
Cotler, Scott J. ;
Denning, Mitchell F. ;
Shimamura, Takashi ;
Breslin, Peter ;
Luescher, Bernhard ;
Qiu, Wei .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2016, 310 (11) :G1155-G1168
[6]   Epigenomic Evaluation of Cholangiocyte Transforming Growth Factor-β Signaling Identifies a Selective Role for Histone 3 Lysine 9 Acetylation in Biliary Fibrosis [J].
Aseem, Sayed Obaidullah ;
Jalan-Sakrikar, Nidhi ;
Chi, Cheng ;
Navarro-Corcuera, Amaia ;
De Assuncao, Thiago M. ;
Hamdan, Feda H. ;
Chowdhury, Shiraj ;
Banales, Jesus M. ;
Johnsen, Steven A. ;
Shah, Vijay H. ;
Huebert, Robert C. .
GASTROENTEROLOGY, 2021, 160 (03) :889-+
[7]   FTO m6A Demethylase in Obesity and Cancer: Implications and Underlying Molecular Mechanisms [J].
Azzam, Sarah Kassem ;
Alsafar, Habiba ;
Sajini, Abdulrahim A. .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (07)
[8]   Histone deacetylase 4 promotes cholestatic liver injury in the absence of prohibitin-1 [J].
Barbier-Torres, Lucia ;
Beraza, Naiara ;
Fernandez-Tussy, Pablo ;
Lopitz-Otsoa, Fernando ;
Fernandez-Ramos, David ;
Zubiete-Franco, Imanol ;
Varela-Rey, Marta ;
Delgado, Teresa C. ;
Gutierrez, Virginia ;
Anguita, Juan ;
Pares, Albert ;
Banales, Jesus M. ;
Villa, Erica ;
Caballeria, Juan ;
Alvarez, Luis ;
Lu, Shelly C. ;
Mato, Jose M. ;
Martinez-Chantar, Maria Luz .
HEPATOLOGY, 2015, 62 (04) :1237-1248
[9]   Epigenetic mechanisms and metabolic reprogramming in fibrogenesis: dual targeting of G9a and DNMT1 for the inhibition of liver fibrosis [J].
Barcena-Varela, Marina ;
Paish, Hannah ;
Alvarez, Laura ;
Uriarte, Iker ;
Latasa, Maria U. ;
Santamaria, Eva ;
Recalde, Miriam ;
Garate, Maria ;
Claveria, Alex ;
Colyn, Leticia ;
Arechederra, Maria ;
Iraburu, Maria J. ;
Milkiewicz, Malgorzata ;
Milkiewicz, Piotr ;
Sangro, Bruno ;
Robinson, Stuart M. ;
French, Jeremy ;
Pardo-Saganta, Ana ;
Oyarzabal, Julen ;
Prosper, Felipe ;
Rombouts, Krista ;
Oakley, Fiona ;
Mann, Jelena ;
Berasain, Carmen ;
Avila, Matias A. ;
Fernandez-Barrena, Maite G. .
GUT, 2021, 70 (02) :388-400
[10]   Circular RNA circPSD3 alleviates hepatic fibrogenesis by regulating the miR-92b-3p/Smad7 axis [J].
Bu, Fang-tian ;
Zhu, Yan ;
Chen, Xin ;
Wang, Ao ;
Zhang, Ya-fei ;
You, Hong-mei ;
Yang, Yang ;
Yang, Ya-ru ;
Huang, Cheng ;
Li, Jun .
MOLECULAR THERAPY-NUCLEIC ACIDS, 2021, 23 :847-862