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c-Jun在肿瘤发生中作用的研究进展 被引量:4

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摘要 c-Jun是核转录激活蛋白1(activation protein,AP-1)家族的组成成员。AP-1蛋白家族主要包括Jun(c-Jun、Jun-B和Jun-D)和Fos(c-Fos、FosB、Fra-1和Fra-2)2个蛋白家族。c-Jun不仅和Jun或Fos家族成员结合,以AP-1的形式发挥生物学功能,也可以单独作为转录因子参与基因转录调控。各种刺激如生长信号、紫外线或环境污染物可以诱导c-Jun活化,活化的c-Jun通过调节靶基因转录,参与增殖、分化和细胞凋亡等多种生理过程。c-Jun功能异常与许多疾病如恶性肿瘤、脑血管病等的发生密切相关。我们主要从增殖、分化、凋亡以及细胞周期等多个方面对c-Jun在肿瘤发生中的作用进行综述。
出处 《中华劳动卫生职业病杂志》 CAS CSCD 北大核心 2008年第4期253-255,共3页 Chinese Journal of Industrial Hygiene and Occupational Diseases
基金 国家自然科学基金项目(30671747,30371206) “973”国家重点基础研究发展规划项目(2002 CB 512905) 美国Philip Morris USA Inc and Philip Morris Intemational项目
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参考文献20

  • 1Sanyal S, Sandstrom D J, Hoeffer CA, et al. AP- 1 function upstream of CREB to control synaptic plasticity in Drosophila. Nature, 2002,416 : 870-874.
  • 2Grondin B,Lefrancois M,Tremblay M, et al. c-Jun homodimers can function as a context-specific coactivator. Mol Cell Biol, 2007,27 : 2919-2933.
  • 3王志强,黄杰,林慧庆,王旭广.癌基因c-fos和c-jun与非小细胞肺癌临床病理特征的相关性研究[J].肿瘤防治研究,2004,31(5):284-285. 被引量:4
  • 4Johnson GL, Nakamura K. The c-Jun kinase/stress-activated pathway: regulation, function and role in human disease. Biochim Biophys Acta,2007, 1773: 1341-1348.
  • 5Vogt PK. Fortuitous convergences: the beginnings of JUN. Nat Rev Cancer, 2002,2: 465-469.
  • 6Behrens A,Sibilia M, David JP,et al. Impaired postnatal hepatocyte proliferation and liver regeneration in mice lacking c-jun in the liver. EMBO J, 2002,21 : 1782-1790.
  • 7Eriksson M,Taskinen M, Leppa S, et al. Mitogen activated protein kinase-dependent activation of c-Jun and c-Fos is required for neuronal differentiation but not for growth and stress response in PC 12 cells. J Cell Physiol, 2007,210: 538-548.
  • 8袁莲香.AP-1在皮肤肿瘤中的表达及其意义[J].中国癌症杂志,2006,16(10):867-869. 被引量:2
  • 9郑明,张伟,汤晓飞,刘敬华.癌基因c-fos,c-jun在口腔鳞癌的表达研究[J].口腔医学研究,2005,21(3):279-282. 被引量:12
  • 10Hettinger K,Vikhanskaya F,Poh MK,et al. c-Jun promotes cellular survival by suppression of PTEN. Cell Death Differ, 2007,14:218-229.

二级参考文献66

  • 1郑明,张伟,汤晓飞,刘敬华.癌基因c-fos,c-jun在口腔鳞癌的表达研究[J].口腔医学研究,2005,21(3):279-282. 被引量:12
  • 2Vogt PK. Jun, the oncoprotein[J]. Oncogene, 2001,20(19):2355-2377
  • 3Hu Y, Cheng L, Hochleitner BW, et al. Activation of mitogen-activated protein kinases (ERK/JNK) and AP-1 transcription actor in rat carotid arteries after balloon injury[J].Arterioscler Thromb Vasc Biol, 1997, 17(11): 2808 - 2816.
  • 4Tabor E. Tumor suppressor genes, growth factor genes, and oncogenes in hepatitis B virus-associated hepatocellular carcinoma[J]. J Med Virol, 1994, 42(4): 357-365.
  • 5Volm M, Effert T, Matter J, et al. Resistance mechanisms in murine tumors with acquired multidrug resistance [J].Arzneimittelforschung, 1992, 42(9): 1163 - 1168.
  • 6Tiniakos DG, Mellon K, Anderson JJ, et al. c-jun oncogene expression in transitional cell carcinoma of the urinary bladder[J]. Br J Urol, 1994,74(6): 757-761.
  • 7Dong ZG, Jeffrey AM. Hydrolysis of carcinogen-DNA adducts by three classes of deoxyribonucleosidase to their corresponding bases[J]. Carcinogenesis, 1991, 12(6): 1125-1128.
  • 8Smeyne RJ, Vendrell M, Hayward M, et al. Continuous c-fos expression precedes programmed cell death in vivo [J]. Nature,1993, 363(6425): 166 - 169.
  • 9Moretta A. Molecular mechanisms in cell-mediated cytotoxicity[J]. Cell, 1997, 90(1): 13 - 18.
  • 10Caelles C, Helmberg A, Karin M. p53-dependent apoptosis in the absence of transcriptional activation of p53-target genes[J].Nature, 1994, 370 (6486): 220-223.

共引文献20

同被引文献71

  • 1叶韵斌,陈强,林建银,刘枋,LIU wang-qing,wang-qing,Michel VIDAL,VIDAL,Christiane GARBAY,GARBAY.Grb2抑制剂对K562细胞生长增生的影响[J].肿瘤研究与临床,2008,20(10):658-664. 被引量:1
  • 2郭光明,王明荣.c-Jun和c-Fos及其与人类肿瘤[J].国外医学(遗传学分册),2005,28(4):207-211. 被引量:15
  • 3赵松,付英梅,赵柏,刘连新.慢性萎缩性胃炎黏膜上皮中P53和C-erbB-2表达的临床意义[J].世界华人消化杂志,2006,14(30):2943-2947. 被引量:10
  • 4Marshall A, Hodgson J. DNA chips: an array of possibilities. Nat Biotechnol, 1998, 16:27-31.
  • 5Ramsay G. DNA chips: state-of-the art. Nat Biotechnol, 1995, 16:40- 44.
  • 6Cussac D, Vidal M, Leprince C, et al. A Sos-derived peptidimer blocksthe Ras signaling pathway by binding both Grb2 SH3 domains and displays antiproliferative activity. FASEB J, 1999, 13:31-38.
  • 7Ye YB, Lin JY, Chen Q, et al. The eytotoxicity of a Grb2-SH3 inhibitor in Bcr-Abl positive K562 ceils. Biochem Pharmacol, 2008, 75:2080- 2091.
  • 8Ye YB, Lin JY, Chen Q, et al. The cytotoxicity of a Grb2-SH3 inhibitor in Bcr-Abl positive K562 cells. Biochem Pharmacol, 2005, 75:2080- 2091.
  • 9Salahshor S, Woodgett JR. The links between axin and carcinogenesis. J Clin Pathol, 2005, 58:225-236.
  • 10Glavic A, Molnar C, Cotoras D, et al. Drosophila Axudl is involved in the control of proliferation and displays pro-apoptotic activity. Mech Dev,2009, 126:184-197.

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