Literature DB >> 28120534

Sulforaphane suppresses cell growth and collagen expression of keloid fibroblasts.

Ayako Kawarazaki1,2, Mano Horinaka1, Shusuke Yasuda1, Toshiaki Numajiri2, Kenichi Nishino2, Toshiyuki Sakai1.   

Abstract

Keloids are fibroproliferative diseases characterized by the accumulation of an extracellular matrix including collagen. Various growth factors, or cytokines, and their receptors are overexpressed in keloids, and they are expected to be therapy targets. Sulforaphane, a dietary isothiocyanate, has recently shown anti-tumor, anti-inflammatory, and anti-fibrotic properties. In this study, we found that sulforaphane inhibited cell growth and reduced collagen at the mRNA and protein levels in keloid fibroblasts. Moreover, sulforaphane markedly suppressed the expression of IL-6 and α-SMA and inhibited Stat3 and Smad3 signaling pathways in keloid fibroblast KF112 cells. Sulforaphane induced G2/M cell-cycle arrest with the induction of p21 in KF112 cells. In addition, sulforaphane inhibited cell growth and suppressed the expression of collagen in keloid fibroblasts under a coculture with peripheral blood mononuclear cells. Furthermore, sulforaphane suppressed IL-6, Stat3, and Smad3 signaling in the coculture system. This study suggests that sulforaphane may be a novel keloid treatment.
© 2017 by the Wound Healing Society.

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Year:  2017        PMID: 28120534     DOI: 10.1111/wrr.12512

Source DB:  PubMed          Journal:  Wound Repair Regen        ISSN: 1067-1927            Impact factor:   3.617


  6 in total

1.  The profibrotic and senescence phenotype of old lung fibroblasts is reversed or ameliorated by genetic and pharmacological manipulation of Slc7a11 expression.

Authors:  Jeffrey D Ritzenthaler; Edilson Torres-Gonzalez; Yuxuan Zheng; Igor N Zelko; Victor van Berkel; David R Nunley; Biniam Kidane; Andrew J Halayko; Ross Summer; Walter H Watson; Jesse Roman
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2022-01-05       Impact factor: 5.464

Review 2.  Advances in the pathogenesis and clinical application prospects of tumor biomolecules in keloid.

Authors:  Yijun Xia; Youbin Wang; Mengjie Shan; Yan Hao; Hao Liu; Qiao Chen; Zhengyun Liang
Journal:  Burns Trauma       Date:  2022-06-25

3.  Antifibrotic effects of sulforaphane treatment on gingival elasticity reduces orthodontic relapse after rotational tooth movement in beagle dogs.

Authors:  Kyong-Nim Kim; Jue-Young Kim; Jung-Yul Cha; Sung-Hwan Choi; Jin Kim; Sung-Won Cho; Chung-Ju Hwang
Journal:  Korean J Orthod       Date:  2020-11-25       Impact factor: 1.372

4.  Effects of the isothiocyanate sulforaphane on TGF-β1-induced rat cardiac fibroblast activation and extracellular matrix interactions.

Authors:  Charity Fix; Amanda Carver-Molina; Mrinmay Chakrabarti; Mohamad Azhar; Wayne Carver
Journal:  J Cell Physiol       Date:  2019-01-04       Impact factor: 6.384

5.  Inhibition of TGF-β2-induced migration and epithelial-mesenchymal transition in ARPE-19 by sulforaphane.

Authors:  Yan-Bing Huang; Ping-Ping Liu; Hui Zheng; Xiu-Xia Yang; Cheng-Cheng Yang; Ye Liu; Yang Liu
Journal:  Int J Ophthalmol       Date:  2021-07-18       Impact factor: 1.779

Review 6.  Fibroblast Growth Factor 2 as an Antifibrotic: Antagonism of Myofibroblast Differentiation and Suppression of Pro-Fibrotic Gene Expression.

Authors:  David M Dolivo; Sara A Larson; Tanja Dominko
Journal:  Cytokine Growth Factor Rev       Date:  2017-09-23       Impact factor: 7.638

  6 in total

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