Histone Deacetylases as Epigenetic Targets for Treating Parkinson’s Disease DOI Creative Commons

Yan Li,

Zhicheng Gu, Shuxian Lin

и другие.

Brain Sciences, Год журнала: 2022, Номер 12(5), С. 672 - 672

Опубликована: Май 21, 2022

Parkinson’s disease (PD) is a chronic progressive neurodegenerative that increasingly becoming global threat to the health and life of elderly worldwide. Although there are some drugs clinically available for treating PD, these treatments can only alleviate symptoms PD patients but cannot completely cure disease. Therefore, exploring other potential mechanisms develop more effective modify course still highly desirable. Over last two decades, histone deacetylases, as an important group epigenetic targets, have attracted much attention in drug discovery. This review focused on current knowledge about deacetylases involved pathophysiology their inhibitors used studies. Further perspectives related small molecules inhibit or degrade treat were also discussed.

Язык: Английский

Targeting epigenetic modifications in Parkinson's disease therapy DOI
Dan Zhang, Jifa Zhang, Yuxi Wang

и другие.

Medicinal Research Reviews, Год журнала: 2023, Номер 43(5), С. 1748 - 1777

Опубликована: Апрель 29, 2023

Abstract Parkinson's disease (PD) is a multifactorial due to complex interplay between genetic and epigenetic factors. Recent efforts shed new light on the mechanisms involved in regulating pathways related development of PD, including DNA methylation, posttranslational modifications histones, presence microRNA (miRNA or miR). Epigenetic regulators are potential therapeutic targets for neurodegenerative disorders. In review, we aim summarize regulation describe how methyltransferases, histone deacetylases, acetyltransferases that mediate key processes PD attractive targets. We discuss use inhibitors and/or activators these models patients, small molecule modulators elicit neuroprotective effects. Further more, given importance miRNAs their contributions underlying will be discussed as well, together with miRNA‐based therapies.

Язык: Английский

Процитировано

16

Journey of Von Hippel-Lindau (VHL) E3 ligase in PROTACs design: From VHL ligands to VHL-based degraders DOI

Nisha Setia,

Haider Thaer Abdulhameed Almuqdadi, Mohammad Abid

и другие.

European Journal of Medicinal Chemistry, Год журнала: 2023, Номер 265, С. 116041 - 116041

Опубликована: Дек. 13, 2023

Язык: Английский

Процитировано

14

Progress of proteolysis-targeting chimeras (PROTACs) delivery system in tumor treatment DOI Creative Commons

Lianlian Fan,

Weifang Tong,

Anhui Wei

и другие.

International Journal of Biological Macromolecules, Год журнала: 2024, Номер 275, С. 133680 - 133680

Опубликована: Июль 4, 2024

Proteolysis targeting chimeras (PROTACs) can use the intrinsic protein degradation system in cells to degrade pathogenic target proteins, and are currently a revolutionary frontier of development strategy for tumor treatment with small molecules. However, poor water solubility, low cellular permeability, off-target side effects most PROTACs have prevented them from passing preclinical research stage drug development. This requires appropriate delivery systems overcome these challenging hurdles ensure precise towards site. Therefore, combination multifunctional will open up new directions targeted proteins. In this review, we systematically reviewed design principles recent advances various systems. Moreover, constructive strategies developing were proposed comprehensively. review aims deepen understanding drugs promote further system.

Язык: Английский

Процитировано

6

Targeted degradation of LRG1 to attenuate renal fibrosis DOI Creative Commons

Linyao Fan,

Yingqiu Qi,

Xi Yang

и другие.

Asian Journal of Pharmaceutical Sciences, Год журнала: 2024, Номер 19(4), С. 100941 - 100941

Опубликована: Июль 10, 2024

Leucine-rich α-2 glycoprotein 1 (LRG1), a secreted glycoprotein, has been identified as significantly upregulated in renal fibrosis, potentially exacerbating the condition by enhancing TGF-β-Smad3-dependent signaling pathways. Herein, utilizing our developed LRG1-targeting peptide for LRG1 recruitment and lenalidomide E3 ubiquitin ligase engagement, we an advanced proteolysis targeting chimera,

Язык: Английский

Процитировано

5

Histone Deacetylases as Epigenetic Targets for Treating Parkinson’s Disease DOI Creative Commons

Yan Li,

Zhicheng Gu, Shuxian Lin

и другие.

Brain Sciences, Год журнала: 2022, Номер 12(5), С. 672 - 672

Опубликована: Май 21, 2022

Parkinson’s disease (PD) is a chronic progressive neurodegenerative that increasingly becoming global threat to the health and life of elderly worldwide. Although there are some drugs clinically available for treating PD, these treatments can only alleviate symptoms PD patients but cannot completely cure disease. Therefore, exploring other potential mechanisms develop more effective modify course still highly desirable. Over last two decades, histone deacetylases, as an important group epigenetic targets, have attracted much attention in drug discovery. This review focused on current knowledge about deacetylases involved pathophysiology their inhibitors used studies. Further perspectives related small molecules inhibit or degrade treat were also discussed.

Язык: Английский

Процитировано

22