The Role of PPAR Gamma in Systemic Sclerosis

Author:

Dantas Andréa Tavares12,Pereira Michelly Cristiny2,de Melo Rego Moacyr Jesus Barreto2,da Rocha Laurindo Ferreira12,Pitta Ivan da Rocha3,Marques Cláudia Diniz Lopes1,Duarte Angela Luzia Branco Pinto1,Pitta Maira Galdino da Rocha2

Affiliation:

1. Serviço de Reumatologia do Hospital das Clínicas da Universidade Federal de Pernambuco (HC-UFPE), 50670-901 Recife, PE, Brazil

2. Laboratório de Imunomodulação e Novas Abordagens Terapêuticas da Universidade Federal de Pernambuco (LINAT-UFPE), 50670-901 Recife, PE, Brazil

3. Laboratório de Planejamento e Síntese de Fármacos da Universidade Federal de Pernambuco (LPSF-UFPE), 50670-901 Recife, PE, Brazil

Abstract

Fibrosis is recognized as an important feature of many chronic diseases, such as systemic sclerosis (SSc), an autoimmune disease of unknown etiology, characterized by immune dysregulation and vascular injury, followed by progressive fibrosis affecting the skin and multiple internal organs. SSc has a poor prognosis because no therapy has been shown to reverse or arrest the progression of fibrosis, representing a major unmet medical need. Recently, antifibrotic effects of PPARγligands have been studiedin vitroandin vivoand some theories have emerged leading to new insights. Aberrant PPARγfunction seems to be implicated in pathological fibrosis in the skin and lungs. This antifibrotic effect is mainly related to the inhibition of TGF-β/Smad signal transduction but other pathways can be involved. This review focused on recent studies that identified PPARγas an important novel pathway with critical roles in regulating connective tissue homeostasis, with emphasis on skin and lung fibrosis and its role on systemic sclerosis.

Publisher

Hindawi Limited

Subject

Pharmacology (medical),Drug Discovery

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