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      KCI등재 SCIE SCOPUS

      Therapeutic effects of histone deacetylase inhibitors on kidney disease

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      https://www.riss.kr/link?id=A105112513

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      다국어 초록 (Multilingual Abstract)

      Increasing evidence has shown the involvementof histone deacetylases (HDACs) in the development andprogression of various renal diseases, highlighting itsinhibition as a promising therapeutic strategy to preventkidney diseases. Accordingly, numerous studies haveshown that HDAC inhibitors protect the kidneys fromvarious diseases through their effects on multiple pathways,such as suppression of transforming growth factor-βsignaling pathway and nuclear factor-κB signaling pathways,augmentation of apoptosis, and inhibition of angiogenesis.
      To develop more effective and less toxic isoformselectiveHDAC inhibitors and further improve clinicaloutcomes, it is necessary to identify and understand themechanisms involved in the pathogenesis and progressionof renal diseases. This review focuses on the roles ofHDAC inhibitors and the mechanisms involved in theirtherapeutic effects in experimental models of kidney diseasesincluding glomerulosclerosis, tubulointerstitialfibrosis, glomerular and tubulointerstitial inflammation,lupus nephritis, polycystic kidney disease, and renal cellcarcinoma (RCC).
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      Increasing evidence has shown the involvementof histone deacetylases (HDACs) in the development andprogression of various renal diseases, highlighting itsinhibition as a promising therapeutic strategy to preventkidney diseases. Accordingly, numerous s...

      Increasing evidence has shown the involvementof histone deacetylases (HDACs) in the development andprogression of various renal diseases, highlighting itsinhibition as a promising therapeutic strategy to preventkidney diseases. Accordingly, numerous studies haveshown that HDAC inhibitors protect the kidneys fromvarious diseases through their effects on multiple pathways,such as suppression of transforming growth factor-βsignaling pathway and nuclear factor-κB signaling pathways,augmentation of apoptosis, and inhibition of angiogenesis.
      To develop more effective and less toxic isoformselectiveHDAC inhibitors and further improve clinicaloutcomes, it is necessary to identify and understand themechanisms involved in the pathogenesis and progressionof renal diseases. This review focuses on the roles ofHDAC inhibitors and the mechanisms involved in theirtherapeutic effects in experimental models of kidney diseasesincluding glomerulosclerosis, tubulointerstitialfibrosis, glomerular and tubulointerstitial inflammation,lupus nephritis, polycystic kidney disease, and renal cellcarcinoma (RCC).

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      참고문헌 (Reference)

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      학술지 인용정보

      학술지 인용정보
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      1.07 0.87 0.439 0.05
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