期刊文献+

组蛋白去乙酰化酶抑制剂在肾脏疾病中的研究进展 被引量:2

Research Advancementsprogress onf the role of histone deacetylase inhibitors in kidney diseases
下载PDF
导出
摘要 组蛋白去乙酰化酶(HDAC)可以诱导组蛋白和非组蛋白去乙酰化,在基因表达的表观遗传调节方面发挥重要作用。越来越多的证据表明HDAC参与各种肾脏疾病的发生、发展,强调抑制其活性可作为肾脏疾病的一种重要治疗策略。该文综述了组蛋白去乙酰化酶抑制剂在肾小管间质纤维化、糖尿病肾病、多囊肾病、急性肾损伤和狼疮性肾炎等肾脏疾病中的作用机制,以期为各种肾脏疾病的临床诊疗提供新靶点。 Histone deacetylase(HDAC)can induce deacetylation of both histone and non-histone proteins,and plays an important role in epigenetic regulation of gene expression.Increasing evidence has shown the involvement of HDAC in the development and progression of various renal diseases,highlighting the inhibition of HDAC as a promising therapeutic strategy to kidney diseases.This review focuses on the potential therapeutic effects and relevant mechanisms of HDAC inhibitors in kidney diseases including tubulointerstitial fibrosis,diabetic nephropathy,polycystic kidney disease,acute kidney injury and lupus nephritis,in order to provide new targets for clinical diagnosis and treatment of various renal diseases.
作者 杨晓鹏 田莎莎 郭珲 Xiao-peng Yang;Sha-sha Tian;Hui Guo(The Second College of Clinical Medicine,Shanxi Medical University,Taiyuan,Shanxi 030001,China;Department of Nephrology,the Second Clinical Medical College,Hospital of Shanxi Medical University,Taiyuan,Shanxi 030001,China)
出处 《中国现代医学杂志》 CAS 北大核心 2021年第2期43-47,共5页 China Journal of Modern Medicine
基金 山西省回国留学人员科研项目(No:2017-116)。
关键词 组蛋白 组蛋白去乙酰化酶 组蛋白去乙酰化酶抑制剂 肾脏疾病 histone histone deacetylase histone deacetylase inhibitor kidney diseases
  • 相关文献

参考文献1

二级参考文献12

  • 1孙辽,余学清,祝胜郎,陈文芳,李哓艳,贾占军,王欣,窦献蕊,董秀清,孙惠力.AGEs对肾小管上皮细胞转分化、1型胶原合成及smad信号通路的影响[J].中国病理生理杂志,2006,22(12):2429-2433. 被引量:13
  • 2TAMAKI K, OKUDA S. Role of TGF-beta in the progression of renal fibrosis[J]. Contrib Nephrol, 2003, 139: 44-65.
  • 3SHEPPARD D. Integrin-mediated activation of latent transforming growth factor beta [J]. Cancer Metastasis Rev, 2005, 24 (3): 395402.
  • 4SHEPPARD D. Integrin-mediated activation of transforming growth factor-beta(1) in pulmonary fibrosis[J]. Chest, 2001, 120 (1): 49S-53S.
  • 5JORDAN A, KREIDBERG, JORDAN M. Integrins in kidney development, function and disease [J]. Am J Physiol Renal Physiol, 2000, 279: 233-242.
  • 6MA LJ,YANG H,GASPERT A, et al. Transforming growth factor-beta-dependent and independent pathways of induction of tubulointerstitial fibrosis in beta6 (-/-) mice [J]. Am J Pathol, 2003, 163(4): 1261-1273.
  • 7HAGIWARA S, MAKITA Y, GU L, et al. Eicosapentaenoic acid ameliorates diabetic nephropathy of type 2 diabetic KKAy/Ta mice: involvement of MCP21 suppression and decreased ERK1 /2 and p38phosphorylation[J]. Nephrol Dial Transp lant, 2006, 21 (3): 605-615.
  • 8HAN DC, HOFFMAN BB, HONG SW, et al. Therapy with antisense TGF-beta1 oligodeoxynucleotides reduces Kidney weight and matrix mRNAs in diabetic mice [J]. Am J Physiol Renal Physiol, 2000, 278:628-634.
  • 9XIONG J P, STEHLE T, ZHANG R, et al. Crystal structure of the extracellular segment of integrin alpha Vbeta3 in complex with an Arg-Gly-Asp ligand[J]. Science, 2002, 296: 151-155.
  • 10HAKKINEN L KOIVISTO L, GARDNERRT H, et al. Increased expression of beta6-integrin in skin leads to spontaneous development of chronic wounds [J]. Am J Pathol, 2004, 164(1): 229-242.

共引文献2

同被引文献8

引证文献2

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部