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叉头转录因子家族与肝纤维化的研究进展 被引量:3

Forkhead box family in liver fibrosis
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摘要 肝纤维化为肝脏炎症或损伤后组织修复过程中的一种代偿反应。肝纤维化的发展与肝代谢失调,肝星状细胞激活与转分化以及细胞外基质沉积密切相关,而这其中涉及大量信号通路的调节。叉头转录因子(Fox)通路对细胞代谢、存活、增殖分化等方面具有重要的调控作用,在肝纤维化不同发展阶段均发挥了重要作用。本文在此对Fox家族参与肝纤维化的相关研究进展进行了综述。 Liver fibrosis is a compensatory response of tissue repairingin chronic liverinjury and inflammation.The development and deterioration of liver fibrosis is related tothe hepatic metabolic disorder,the activation and transdifferentiation of hepatic stellate cells and the deposition of extracellular matrix.This periodinvolves the complicatedregulations of a large number of signal pathways.Among those pathways,the Forkhead box(Fox)family plays an important role in regulating cell metabolism,apoptosis,proliferation and differentiationin different stages of liver fibrosis.This study reviewed the research progress of the Fox family involved in liver fibrosis.
作者 赵治锋 罗蒙 Zhao Zhifeng;Luo Meng(Department of General Surgery,Shanghai Ninth People’s Hospital,Shanghai Jiaotong University School of Medicine,Shanghai 200011,China)
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2020年第10期1949-1955,共7页 Chinese Journal of Experimental Surgery
基金 国家自然科学基金(81970526、81770599) 上海交通大学医学院附属第九人民医院临床研究助推计划(JYLJ021) 上海交通大学医学院转化医学协同创新中心合作研究项目(TM201804)。
关键词 肝纤维化 叉头转录因子 肝星状细胞 Liver fibrosis Forkhead box Hepatic stellate cells
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  • 1陆明,刘丽梅.翼螺旋转录因子Foxa2与糖脂代谢及糖尿病关系的研究进展[J].上海交通大学学报(医学版),2011,31(4):497-500. 被引量:3
  • 2曹冬梅,卢建.叉头框(Fox)转录因子家族的结构与功能[J].生命科学,2006,18(5):491-496. 被引量:36
  • 3Abrams EW, Andrew D J, 2005. CrebA regulates secretory activity in the Drosophila salivary gland and epidermis. Development, 132 (12) 2743 - 2758.
  • 4Abrams EW, Mihoulides WK, Andrew D J, 2006. Fork head and Sage maintain a uniform and patent salivary gland lumen through regulation of two downstream target genes, PH4alphaSG1 and PH4alphaSG2. Development, 133 ( 18 ) : 3517 - 3527.
  • 5Ariani F, Hayek G., Rondinella D, Artuso R, Mencarelli MA, Spanhol- Rosseto A, Pollazzon M, Buoni S, Spiga O, Ricciardi S, Meloni I, Longo I, Marl F, Broccoli V, Zappella M, Renieri A, 2008. FOXG1 is responsible for the congenital variant of Rett syndrome. American Journal of Human Genetics, 83 (1) : 89 -93.
  • 6Azzaria M, Goszczynski B, Chung MA, Kalb JM, McGhee JD, 1996. A fork head/HNF-3 homolog expressed in the pharynx and intestine of the Caenorhabditis elegans embryo. Dev. Biol., 178(2) : 289 -303.
  • 7Bahi-Buisson N, Nectoux J, Girard B, Van Esch H, De Ravel T, Boddaert N, Plouin P, Rio M, Fichou Y, Chelly J, Bienvenu T, 2010. Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant. Neurogenetics, 11 ( 2 ) : 241 - 249.
  • 8Benayoun BA, Caburet S, Veitia RA, 2011. Forkhead transcription factors: key players in health and disease. Trends in Genetics, 27 (6) : 224 - 232.
  • 9Berry FB, Saleem RA, Walter MA, 2002. FOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domain. J. Biol. Chem., 277(12) : 10292 - 10297.
  • 10Bredenkamp N, Seoighe C, Illing N, 2007. Comparative evolutionary analysis of the FoxG1 transcription factor from diverse vertebrates identifies conserved recognition sites for microRNA regulation. Dev. Genes Evol., 217(3) : 227 -233.

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