期刊文献+

Prospective of extracellular matrix and drug correlations in disease management

下载PDF
导出
摘要 The extracellular matrix(ECM)comprises of many structural molecules that constitute the extracellular environment.ECM molecules are characterized by specific features like diversity,complexity and signaling,which are also results of improvement or development of disease mediated by some physiological changes.Several drugs have also been used to manage diseases and they have been reported to modulate ECM assembly,including physiological changes,beyond their primary targets and ECM metabolism.This review highlights the alteration of ECM environment for diseases and effect of different classes of drugs like nonsteroidal anti-inflammatory drugs,immune suppressant drug,steroids on ECM or its components.Thus,it is summarized from previously conducted researches that diseases can be managed by targeting specific components of ECM which are involved in the pathophysiology of diseases.Moreover,the drug delivery focused on targeting the ECM components also has the potential for the discovery of targeted and site specific release of drugs.Therefore,ECM or its components could be future targets for the development of new drugs for controlling various disease conditions including neurodegenerative diseases and cancers.
作者 Varish Ahmad
出处 《Asian Journal of Pharmaceutical Sciences》 SCIE CAS 2021年第2期147-160,共14页 亚洲药物制剂科学(英文)
  • 相关文献

参考文献3

二级参考文献143

  • 1[1]Uitto J,Kouba D.Cytokine modulation of extracellular matrix gene expression:relevance to fibrotic skin diseases.J Dermatol Sci 2000; 24 Suppl 1:S60-S69
  • 2[2]Verrecchia F,Mauviel A.TGF-beta and TNF-alpha:antagonis tic cytokines controlling type I collagen gene expression.Cell Signal 2004; 16:873-880
  • 3[3]Verrecchia F,Mauviel A.Control of connective tissue gene expression by TGF beta:role of Smad proteins in fibrosis.Curr Rheumatol Rep 2002; 4:143-149
  • 4[4]Verrecchia F,Mauviel A.Transforming growth factor-beta signaling through the Smad pathway:role in extracellular matrix gene expression and regulation.J Invest Dermatol 2002; 118:211-215
  • 5[5]LeRoy EC,Trojanowska MI,Smith EA.Cytokines and human fibrosis.Eur Cytokine Netw 1990; 1:215-219
  • 6[6]Schiller M,Javelaud D,Mauviel A.TGF-beta-induced SMAD signaling and gene regulation:consequences for extracellular matrix remodeling and wound healing.J Dermatol Sri 2004; 35:83-92
  • 7[7]Grotendorst GR.Connective tissue growth factor:a mediator of TGF-beta action on fibroblasts.Cytokine Growth Factor Rev 1997; 8:171-179
  • 8[8]Leask A,Denton CP,Abraham DJ.Insights into the molecular mechanism of chronic fibrosis:the role of connective tissue growth factor in scleroderma.J Invest Dermatol 2004; 122:1-6
  • 9[9]Feng XH,Derynck R.Specificity and versatility in tgf-beta signaling through Smads.Annu Rev Cell Dev Biol 2005; 21:659-693
  • 10[10]Roberts AB.Molecular and cell biology of TGF-beta.Miner Electrolyte Metab 1998; 24:111-119

共引文献137

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