期刊文献+

FOXC1在肿瘤进展中的作用 被引量:2

Role of FOXC1 in the progression of tumors
下载PDF
导出
摘要 FOXC1是转录因子FOX超家族的成员,广泛存在于人体的多种组织和器官中,参与胚胎时期眼睛、心脏、肾、脑膜、骨骼发育的调控。作为转录因子,FOXC1蛋白通过作用于靶基因的启动子或与其他转录因子相互作用激活转录,并从上皮-间质转化、细胞信号转导和血管内皮细胞迁移等多方面影响肿瘤细胞的生长周期和增殖活动。FOXC1参与多种肿瘤的发生和发展的过程,其表达的水平还可作为某些肿瘤预后评估的指标,并有望成为肿瘤靶向治疗的新位点。 FOXC1 is a member of transcription factor forhead box(FOX) protein superfamily.FOXC1 gene widely exists in human tissues and participates in the developmental regulation of eye,heart,kidney,meninx,and skeleton during embryonic development stage. As a transcription factor,FOXC1 protein activiates the transcription through acting on promoters of the target genes or interacting with other transcription factors.Additionally,it affects the cell cycle and proliferation of tumor cells by epithelial-to-mesenchymal transition,cellular signal transduction,migration of vascular endothelial cell,etc.FOXC1 is involved in the occurrence and development of various tumors.The expression level of FOXC1 can be used as a prognostic index in evaluation of some types of tumors.Hopefully,it may be considered as a novel target for therapy.
作者 谢永辉 张声
出处 《国际病理科学与临床杂志》 CAS 2011年第5期434-438,共5页 Journal of International Pathology and Clinical Medicine
基金 福建医科大学第一临床学院学科带头人培养对象专项基金(JXK200724)~~
关键词 FOXC1 肿瘤 上皮-间质转化 转化生长因子Β1 趋化因子受体4 FOXC1 tumor epithelial-to-mesenchymal transition transforming growth factor β1 chemokine receptor 4
  • 相关文献

参考文献28

  • 1Nishimura DY, Swiderski RE, Alward WLM, et al. The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25 [J]. Nat Genet, 1998, 19 (7) : 140 -147.
  • 2Lehmann OJ, Sowden JC, Carlsson P, et al. Fox's in development and disease [J]. Trends Cenet, 2003,19 ( 6 ) :339-344.
  • 3Berry FB, Saleem RA, Walter MA. FOXC1 tanscriptional regulation is mediated by N-and C-terminal activationdomains and con- tains a phyophorylated transcriptional inhibitory domain [J]. Biol Chem, 2007, 277(12): 10292-10297.
  • 4Kaestner KH, Knochel W, Martinez DE. Unified nomenclature for the winged helix/forkhead transcription factors [ J ]. Genes Dev, 2000,14(2) :142-146.
  • 5Nishimura DY, Searby CC, Alward WL, et al. A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye [ J ]. Am J Hum Genet, 2001, 68(2) : 364-372.
  • 6Tanwar M, Kumar M, Dada T, et al. MYOC and FOXC1 gene analysis in primary congenital glaucoma[J]. Mol Vis, 2010, 16 (5) : 1996-2006.
  • 7Tiimer Z, Bach-Holm D. Axenfeld-Rieger syndrome and spectrum of PITX2 and FOXC1 mutations[J]. Eur J Hum Genet, 2009, 17(12): 1527-1539.
  • 8Aldinger KA, Lehmann OJ, Hudgins L, et al. FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25. 3 Dandy-Walker malformation [ J ]. Nat Genet, 2009, 41 (9) : 1037-1042.
  • 9Kume T. The cooperative roles of Foxcl and Foxc2 in cardiovascular development [ J ]. Med Biol, 2009, 665 (2) : 63-77.
  • 10Nakano T, Niimura F, Hohenfellner K, et al. Screening for mu- tations in BMP4 and FOXC1 genes in congenital anomalies of the kidney and urinary tract in humans[J]. Tokai J Exp Clin Med, 2003, 28(3) : 121-126.

二级参考文献16

  • 1Mears A J,Jordan T,Mirzayans F,et al.Mutations of the forkhead/ winged-helix gene,FKHL7,in patients with Axenfeld-Rieger anomaly[J].Am J Hum Genet,1998,63 (5):1316-1328.
  • 2Nishimura D Y,Swiderski R E,Alward W L,et al.The forkheed transcription factor gene FKHL7 is responsible for glaucooma phenotypes which map to 6p25[J].Nat Genel,1998,19(2):140-147.
  • 3Gould D B,Mears A J,Pearce W G,et al.Autosomal dominant Ax enfeld-Rieger anomaly maps to 6p25[J].Am J Hum Genet,1997,61 (3):765-768.
  • 4Mirzayans F,Meats A J,Guo S W,et al.Identification of the human chromosomal region containing the iridogoniodysgenesis anomaly locus by genomic-mismatch scanning[J].Am J Hum Genet,1997,61 (1):111-119.
  • 5Kume T,Deng K Y,Winfrey V,et al.The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus[J].Cell,1998,93 (6):985-996.
  • 6Kidson S H,Kume T,Deng K Y,et al.The forkhead/winged-helix gene,Mf1,is necessary for the normal development of the cornea and for mation of the anterior chamber in the mouse eye[J].Dev Biol,1999,211(2):306-322.
  • 7Smith R S,Zabaleta A,Kume T,et al.Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development[J].Hum Mol Genet,2000,9(7):1021-1032.
  • 8Kume T,Dang K Y,Hogan B L.Murine forkhead/winged helix genes Foxel (Mf1) and Foxe2 (Mfh1) are required for the early organogenesis of the kidney and urinary tract[J].Development,2000,127(7):1387-1395.
  • 9Zhou Y,Kato H,Asanoma K,et al.Identification of FOXC1 as a TGF-betal responsive gene and its involvement in negative regulation of cell growth[J].Genomics,2002,80(5):465-472.
  • 10Van der Heul-Nieuwenhuijsen L,Dits N F,Jenster G.Gene expression of forkhead transcription factors in the normal and diseased human prostate[J].BJU Int,2009,103(11):1574-1580.

共引文献9

同被引文献7

引证文献2

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部