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TGF-β Inhibitors for Therapeutic Management of Kidney Fibrosis.

Cheol Ho ParkTae-Hyun Yoo
Published in: Pharmaceuticals (Basel, Switzerland) (2022)
Kidney fibrosis is a common pathophysiological mechanism of chronic kidney disease (CKD) progression caused by several underlying kidney diseases. Among various contributors to kidney fibrosis, transforming growth factor-β1 (TGF-β1) is the major factor driving fibrosis. TGF-β1 exerts its profibrotic attributes via the activation of canonical and non-canonical signaling pathways, which induce proliferation and activation of myofibroblasts and subsequent accumulation of extracellular matrix. Over the past few decades, studies have determined the TGF-β1 signaling pathway inhibitors and evaluated whether they could ameliorate the progression of CKD by hindering kidney fibrosis. However, therapeutic strategies that block TGF-β1 signaling have usually demonstrated unsatisfactory results. Herein, we discuss the therapeutic concepts of the TGF-β1 signaling pathway and its inhibitors and review the current state of the art regarding regarding TGF-β1 inhibitors in CKD management.
Keyphrases
  • transforming growth factor
  • epithelial mesenchymal transition
  • signaling pathway
  • chronic kidney disease
  • extracellular matrix
  • end stage renal disease
  • pi k akt
  • liver fibrosis
  • cell proliferation
  • case control