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Diverse Role of TGF-β in Kidney Disease
by
Lan, Hui-Yao
, Gu, Yue-Yu
, Yu, Xue-Qing
, Liu, Xu-Sheng
, Huang, Xiao-Ru
in
Cell and Developmental Biology
/ Fibrosis
/ Growth factors
/ Inflammation
/ Kidney diseases
/ Kinases
/ mechanisms
/ Non-coding RNA
/ Phosphorylation
/ Proteins
/ Roles
/ Smad protein
/ Smad3 protein
/ Smad7 protein
/ Smads
/ TGF-β
/ therapy
/ Transcriptomes
/ Transforming growth factor-b
/ Transforming growth factor-b1
2020
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Diverse Role of TGF-β in Kidney Disease
by
Lan, Hui-Yao
, Gu, Yue-Yu
, Yu, Xue-Qing
, Liu, Xu-Sheng
, Huang, Xiao-Ru
in
Cell and Developmental Biology
/ Fibrosis
/ Growth factors
/ Inflammation
/ Kidney diseases
/ Kinases
/ mechanisms
/ Non-coding RNA
/ Phosphorylation
/ Proteins
/ Roles
/ Smad protein
/ Smad3 protein
/ Smad7 protein
/ Smads
/ TGF-β
/ therapy
/ Transcriptomes
/ Transforming growth factor-b
/ Transforming growth factor-b1
2020
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Diverse Role of TGF-β in Kidney Disease
by
Lan, Hui-Yao
, Gu, Yue-Yu
, Yu, Xue-Qing
, Liu, Xu-Sheng
, Huang, Xiao-Ru
in
Cell and Developmental Biology
/ Fibrosis
/ Growth factors
/ Inflammation
/ Kidney diseases
/ Kinases
/ mechanisms
/ Non-coding RNA
/ Phosphorylation
/ Proteins
/ Roles
/ Smad protein
/ Smad3 protein
/ Smad7 protein
/ Smads
/ TGF-β
/ therapy
/ Transcriptomes
/ Transforming growth factor-b
/ Transforming growth factor-b1
2020
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Journal Article
Diverse Role of TGF-β in Kidney Disease
2020
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Overview
Inflammation and fibrosis are two pathological features of chronic kidney disease (CKD). Transforming growth factor-β (TGF-β) has been long considered as a key mediator of renal fibrosis. In addition, TGF-β also acts as a potent anti-inflammatory cytokine that negatively regulates renal inflammation. Thus, blockade of TGF-β inhibits renal fibrosis while promoting inflammation, revealing a diverse role for TGF-β in CKD. It is now well documented that TGF-β1 activates its downstream signaling molecules such as Smad3 and Smad3-dependent non-coding RNAs to transcriptionally and differentially regulate renal inflammation and fibrosis, which is negatively regulated by Smad7. Therefore, treatments by rebalancing Smad3/Smad7 signaling or by specifically targeting Smad3-dependent non-coding RNAs that regulate renal fibrosis or inflammation could be a better therapeutic approach. In this review, the paradoxical functions and underlying mechanisms by which TGF-β1 regulates in renal inflammation and fibrosis are discussed and novel therapeutic strategies for kidney disease by targeting downstream TGF-β/Smad signaling and transcriptomes are highlighted.
Publisher
Frontiers Media SA,Frontiers Media S.A
Subject
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