期刊文献+

转录因子叉头框Q1与肿瘤相关性的研究进展 被引量:8

Progress in research on the transcription factor forkhead box Q1 in relation to malignant tumors
原文传递
导出
摘要 转录因子叉头框Q1(forkhead box Q1,FOXQ1)是叉头框(forkhead box,FOX)超家族的成员之一,广泛存在于人体的多种组织和器官,参与胚胎干细胞和脊椎动物的发育过程。作为转录因子,FOXQ1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靶基因的转录,并从上皮-间质转化(epithelial-mesenchymal transition,EMT)和细胞信号转导等多方面影响肿瘤的发生、发展、侵袭和转移过程。鉴于FOXQ1与肿瘤具有明显相关性,其表达水平可作为某些肿瘤预后评估的指标,并有望成为肿瘤治疗的新靶点。本文通过综述最新文献,着重阐述了FOXQ1在肿瘤发生和发展过程中的作用及其可能的机制,以期为肿瘤治疗和研究提供一些参考。 The transcription factor forkhead box Q1 (FOXQ1), a member of foxhead box superfamily, widely exists in human tissues and organs, and it is involved in development process of embryonic stem cells and vertebrate. As a transcription factor, FOXQ1 protein activates the transcription by acting on promoter of target genes or interacting with other transcription factors, and it affects initiation, progression, invasion and metastasis of tumor cells in many aspects such as epithelial-mesenchymal transition (EMT) and cellular signal transduction. According to the relationship between FOXQ1 and tumors, the expression level of FOXQ1 can be used as a prognostic index for patients with certain tumors, and FOXQ1 is expected to be a novel target for tumor therapy. This review focuses on the role of FOXQ1 in initiation and progression of certain tumors as well as its potential mechanism, aiming to provide the valuable reference for anticancer treatment and research.
出处 《肿瘤》 CAS CSCD 北大核心 2014年第7期662-667,共6页 Tumor
基金 国家自然科学基金资助项目(编号:81173174 81202655) 国家科技支撑计划课题(编号:2008BAI51B02) 教育部高等学校博士学科点专项科研基金(编号:20113237110008)
关键词 肿瘤 叉头转录因子类 细胞转化 肿瘤 信号传导 FOXQ1 Neoplasms Forkhead transcription factors Cell transformation, neoplasms Signal transduction FOXQ1
  • 相关文献

参考文献2

二级参考文献92

  • 1程大丽,陈冬,陈浩阳,张淑兰.核转录因子κBp65在子宫颈鳞癌中的表达及意义[J].中国医科大学学报,2005,34(2):140-142. 被引量:2
  • 2Boulet G, Horvath C, Vanden Broeck D,Sahebali S,Bogers J. Human Papillomavirus:E6 and E7 oncogenes[J]. Int J Biochem Cell Biol, 2007, 39:2006-2011.
  • 3Liu X, Clements A, Zhao K H, Marmorstein R. Structure of the human Papillomavirus E7 oncoprotein and its mechanism for inactivation of the retinoblastoma tumor suppressor[J]. J Biol Chem,2006, 281: 578-586.
  • 4Niu X Y, Peng Z L, Duan W Q, Wang H, Wang P. Inhibition of HPV 16 E6 oncogene expression by RNA interference in vitro and in vivo [J]. Int J Gynecol Cancer, 2006,16 : 743-751.
  • 5Fidan I, Bozdayi G, Rota S, Biri A, Gurelik F C, Yuksel S, et al. The relationship between cervical human papillomavirus infection and apoptosis[J]. Clin Invest Med,2008,31:168-175.
  • 6Wu L, Goodwin E C, Naeger L K, Vigo E, Galaktionov K, Helin K, et al. E2F Rb complexes assemble and inhibit cdc25A transcription in cervical carcinoma cells following repression of human papillomavirus oncogene expression[J]. Mol Cell Biol, 2000,20 :7059-7067.
  • 7James M A, Lee J H, Klingelhutz A J. Human papillomavirus type 16 E6 activates NF-kappaB, induces elAP-2 expression, and protects against apoptosis in a PDZ binding motif-depend ent manner[J]. J Virol, 2006,80:5301-5307.
  • 8Hong H K, Noveroske J K, Headon D J, Liu T, Sy M S,Justice M J, et al. The winged helix/forkhead transcription factor Foxql regulates differentiation of hair in satin mice[J]. Genesis,2001, 29:163-171.
  • 9Hoggatt A M, Kriegel A M, Smith A F, Herring B P. Hepatoeyte nuclear factor-3 homologue 1 ( HFH-1 ) represses tran seription of smooth muscle-specific genes [J]. J Biol Chem, 2000, 275: 31162-31170.
  • 10Jensen E H, Lewis J M, MeLoughlin J M, Alvarado M D, Daud A, Messina J, et al . Down-regulation of pro-apoptotie genes is an early event in the progression of malignant melanoma[J]. AnnSurgOneol,2007, 14: 1416-1423.

共引文献46

同被引文献42

引证文献8

二级引证文献13

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