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调控组蛋白乙酰化水平抑制膀胱癌细胞机理的研究进展 被引量:1

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摘要 几乎人类每一类肿瘤的发生都与细胞组蛋白去乙酰化水平异常,RB/E2F细胞周期调控通路被打乱,p21waf/cif1转录被抑制有关。p21waf/cif1是细胞增殖周期中极其重要的周期调控蛋白,对肿瘤增殖有关键的抑制作用。以组蛋白的调控为切入点,以RB和p21waf/cif1为枢纽,研究细胞增殖周期抑制膀胱癌细胞增殖的机理。
出处 《现代肿瘤医学》 CAS 2008年第5期871-873,共3页 Journal of Modern Oncology
基金 深圳市科技计划项目(编号:200404174)
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  • 1Grunstein M. Histone acetylation inchromatin structure and transcription[J]. Nature, 1997,389:349-352.
  • 2Bronell JE, Zhou J, Ranalli T, et al. Tetrahymena histone acetyltransferase A: ahomolog to yeast Gcn5p linking histone acetylation to gene activation[J].Cell,1996,84:843-851.
  • 3Ogryzko W, Schiltz RL, Rusanova V, et al. The transcriptional coactivators p300 andCBP are histone acetyltransfeases[J].Cell,1996,87:953-959.
  • 4Mizzen CA, Yang Y, Dai P, et al. The TAF250 subunit of TFⅡD has histoneacetyltransferase activity[J]. Cell, 1996,87:1261-1270.
  • 5Chen H, Lin RJ, Schiltz RL, et al. Nuclear receptor coactivator ACTR is a novelhistone acetyltransferase and forms a multimeric activation complex with P/CAF andCBP/p300[J].Cell,1997,90:569-580.
  • 6Li H,Gomes PJ,Chen JD.RAC3, a steroid/nuclear receptor-associated coactivator thatis related to SRC-1 and TIF2[J]. Proc Natl Acad Sci USA, 1997,94:8479-8484.
  • 7Hilfiker A,Hilfiker-Kleiner D,Pannuti A, et al. Mof, a putative acetyltransferasegene related to the Tip 60 and MOZ human genes and to the SAS genes of yeast, is requiredfor dosage compensation in Drosopila[J].EMBO J,1998,17:2886-2893.
  • 8Dutnal RN,Tafrov ST,Sternglanz R,et al.Structure of the histone acetyltransferseHat1: a paradigm for the GCN5-related N-acetyltransferasesuperfamily[J].Cell,1998,94:427-438.
  • 9Imhof A, Yang XJ, Ogryzko Q,et al. Acetylation of general transcription factors byhistone acetyltransferases[J]. Curr Biol,1997,7:689-692.
  • 10Gu W, Roeder RG. Activation of p53 sequence-specific DNA binding by acetylation ofthe p53 C-terminal domain[J].Cell,1997,90:595-606.

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  • 1谢爱华,廖晨钟,李伯玉,山松,邓沱,李志斌,宁志强,胡伟明,石乐明,周家驹,鲁先平.以组蛋白去乙酰化酶为靶标的抗癌药物研发进展[J].中国新药杂志,2005,14(1):10-14. 被引量:8
  • 2王生余,张旭辉,于晓妉.新型抗肿瘤药物组蛋白去乙酰化酶抑制剂[J].国际肿瘤学杂志,2006,33(6):404-406. 被引量:12
  • 3NELSON S M,FERGUSON L R,DENNY W A.DNA and the chromosome-varied targets for chemotherapy[J].Cell Chromosome,2004,3(1):2.
  • 4GOLDBERG A D,ALLIS C D,BERNSTEIN E.Epigenetics:a landscape takes shape[J].Cell,2007,128(4):635-638.
  • 5MINUCCI S,PELICCI P G.Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer[J].Nat Rev Cancer,2006,6(1):38-51.
  • 6GREGORETTI I V,LEE Y M,GOODSON H V.Molecular evolution of the histone deacetylase family:functional implications of phylogenetic analysis[J].J Mol Biol,2004,338(1):17-31.
  • 7BLANDER G,GUARENTE L.The Sir2 family of protein deacetylases[J].Annu Rev Biochem,2004,73(5):417-435.
  • 8PFLUM M K,TONG J K,LANE W S,et al.Histone deacetylase 1 phosphorylation promotes enzymatic activity and complex formation[J].J Biol Chem,2001,276(50):47733-47741.
  • 9BOTTOMLEY M J,LO SURDO P,DI GIOVINE P,et al.Structural and functional analysis of the human HDAC4 catalytic domain reveals a regulatory structural Zinc-binding domain[J].J Biol Chem,2008,283(39):26694-26704.
  • 10TONG J J,LIU Jian-hong,BERTOS N R,et al.Identifi-cation of HDAC10,a novel class II human histone deacetylase containing a leucine-rich domain[J].Nuc Aci Res,2002,30(5):1114-1123.

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