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Pirfenidone inhibits proliferation, arrests the cell cycle, and downregulates heat shock protein-47 and collagen type I in rat hepatic stellate cells in vitro.
Xiang, Xian-Hong; Jiang, Tian-Peng; Zhang, Shuai; Song, Jie; Li, Xing; Yang, Jian-Yong; Zhou, Shi.
Afiliación
  • Xiang XH; Department of Interventional Radiology, The First Affiliated Hospital of Sun Yat­Sen University, Guangzhou, Guangdong 510080, P.R. China.
  • Jiang TP; Department of Interventional Radiology, Affiliated Hospital of Guiyang Medical College, Guiyang, Guizhou 550000, P.R. China.
  • Zhang S; Department of Interventional Radiology, Affiliated Cancer Hospital of Guiyang Medical College, Guiyang, Guizhou 550000, P.R. China.
  • Song J; Department of Interventional Radiology, Affiliated Hospital of Guiyang Medical College, Guiyang, Guizhou 550000, P.R. China.
  • Li X; Department of Interventional Radiology, Affiliated Hospital of Guiyang Medical College, Guiyang, Guizhou 550000, P.R. China.
  • Yang JY; Department of Interventional Radiology, The First Affiliated Hospital of Sun Yat­Sen University, Guangzhou, Guangdong 510080, P.R. China.
  • Zhou S; Department of Interventional Radiology, Affiliated Hospital of Guiyang Medical College, Guiyang, Guizhou 550000, P.R. China.
Mol Med Rep ; 12(1): 309-14, 2015 Jul.
Article en En | MEDLINE | ID: mdl-25738437
Pirfenidone (esbiret) is an established anti-fibrotic and anti-inflammatory drug used to treat idiopathic pulmonary fibrosis. In the present study, the dose-dependent effects of pirfenidone on the cell cycle, proliferation and expression of heat shock protein (HSP)-47 and collagen type I in a cultured rat hepatic stellate cell line (HSC-T6) were investigated. Following pirfenidone treatment, cell proliferation was determined using the cell counting kit-8 assay and the cell cycle was measured using flow cytometry. HSP-47 expression was estimated using western blot analysis and collagen type I mRNA was assessed using reverse transcription quantitative polymerase chain reaction. Pirfenidone induced significant dose-dependent inhibition of proliferation in HSC-T6 cells. Cell viability was unaffected by treatment with pirfenidone (0, 10 or 100 µM) for 24 and 72 h. However, after 24 h, HSC-T6 cells exhibited dose-dependent decreases in HSP-47 protein and collagen I mRNA levels. In conclusion, pirfenidone inhibited HSC-T6 cell proliferation, arrested the cell cycle and reduced the expression of HSP-47 and collagen type I, indicating that pirfenidone may be a promising drug in the treatment of liver fibrosis.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Piridonas / Regulación hacia Abajo / Antiinflamatorios no Esteroideos / Colágeno Tipo I / Proliferación Celular / Proteínas del Choque Térmico HSP47 Límite: Animals Idioma: En Revista: Mol Med Rep Año: 2015 Tipo del documento: Article Pais de publicación: Grecia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Piridonas / Regulación hacia Abajo / Antiinflamatorios no Esteroideos / Colágeno Tipo I / Proliferación Celular / Proteínas del Choque Térmico HSP47 Límite: Animals Idioma: En Revista: Mol Med Rep Año: 2015 Tipo del documento: Article Pais de publicación: Grecia