期刊文献+

Ku80蛋白在乳腺癌组织中的表达及其临床意义 被引量:4

The Expression and Significance of Ku80 in the Tissue ofBreast Carcinoma
下载PDF
导出
摘要 研究Ku80蛋白在乳腺癌的表达及与临床病理特征的关系。方法:采用免疫组化法检测65例乳腺癌组织Ku80、ER、PR、HER-2和突变型p53表达水平。结果:65例乳腺癌标本中Ku80、ER、PR、HER-2、p53阳性率分别为78.5%、40.0%、53.8%、44.6%和32.3%。Ku80表达水平与肿瘤大小、ER、PR、HER-2和p53的表达水平有关(P<0.05),其中Ku80与HER-2密切相关(rs=0.319,P=0.010)。结论:Ku80表达水平与影响乳腺癌患者预后的生物学特征相关,特别是与HER-2关系密切;Ku80与HER-2之间可能存在调控通路。 Objective: To study the expression of Ku80 in breastal carcinoma and to explore the correlation between the expression of Ku80 and the characters of clinic, pathology and biology. Methods: Immunohistochemistry was used to measure the expression of Ku80, ER, PR, HER-2 and mutant p53 in 65 cases of breast carcinoma. Results: The expression of Ku80 was 78.5% and was associated with the tumor size and the expressions of ER, PR, HER-2 and mutant p53 (P<0.05). It was positively correlated with HER-2(rs=0.319, P=0.010). Conclusions: The expression of Ku80 in breast carcinoma had close relationship with prognosis factors, especially with HER-2; there may be a modulation pathway between Ku80 and HER-2.
出处 《中国肿瘤临床》 CAS CSCD 北大核心 2004年第10期587-589,共3页 Chinese Journal of Clinical Oncology
关键词 KU80 HER-2 乳腺癌 预后 免疫组织化学 Ku80 HER-2 Breast carcinoma Prognosis Immunohistochemistry
  • 相关文献

参考文献10

  • 1Coffey G, Campbell C. An alternate form of Ku80 is required for DNA end-binding activity in mammalian mitochondria [J]. Nucleic Acids Research, 2000, 28(19): 3793-3800
  • 2Kim CH, Park SJ, Lee SH. A Targeted Inhibition of DNA-Dependent Protein Kinase Sensitizes Breast Cancer Cells Following Ionizing Radiation[J]. J Pharmacol Exp Ther, 2002, 303 (2): 753-759
  • 3Dai Y, Kysela B, Hanakahi LA, et al. Nonhomologous end joining and V (D)J recombination require an additional factor [J].PNAS, 2003, 100(5):2462- 2467
  • 4Manabu K. Dimerization, Translocation and Localization of Ku70and Ku80 Proteins[J].J Radiat Res, 2002, 43:223-236
  • 5Wilson CR, Davidson SE, Margison GP, et al. Expression of Ku70 correlation with survival in carcinoma of the cervix [J]. Br J Cancer, 2000, 83(12): 1702-1706
  • 6Korabiowska M, Tscherny M, Scherry M, et al. Differential expression of DNA nonhomologous end-joining proteins Ku70 and Ku80 in melanoma progression[J]. Mod Pathol, 2002, 15(4):426-433
  • 7GibbsJB. Anticancer drug targets: growth factors and growth factor signaling[J]. Nucleic Acids Res, 2000, 28(19):3793-3800
  • 8Pietras RJ, Poen JC, Gallardo D, et al. Monoclonal antibody to HER-2/neureceptor modulates repair of radiation-induced DNA damage and enhances radiosensitivity of human breast cancer cells overexpressing this oncogene [J]. Cancer Res, 1999, 59(6):1347~13
  • 9Lim DS, Vogel H, Dennis M. Analysis of ku80-Mutant Mice and Cells with Deficient Levels of p53[J]. Molecular and Cellular Biology, 2000, 20(11): 3772-3780
  • 10Smith GG, Jackson SP. The DNA-dependent protein kinase[J].Genes Dev, 1999, 13(8):916-934

共引文献1

同被引文献26

  • 1熊华,于世英,张孟贤.短干扰RNA抑制人宫颈癌HeLa细胞Ku80基因表达[J].华中科技大学学报(医学版),2006,35(3):400-402. 被引量:1
  • 2Collis S J, DeWeese T L, Jeggo P A, et al. The life and death of DNA-PK [J]. Oncogene, 2005,24(6) :949-961.
  • 3Koike M. Dimerization, translocation and localization of Ku70 and Ku80 proteins [ J ]. J Radiat Res (Tokyo), 2002,43 (3) :223-236.
  • 4Brummelkamp T R, Bemards R, Agami R. A system for stable expression of short interfering RNAs in mammalian cells [J]. Science, 2002,296(5567) :550-553.
  • 5Lieber M R, Ma Y, Pannicke U, et al. Mechanism and regulation of human non-homologous DNA end-joining [J]. Nat Rev Mol Cell Biol, 2003,4(9) :712-720.
  • 6Valerie K, Povirk L F. Regulation and mechanisms of mammalian double-strand break repair [J]. Oncogene, 2003, 22 (37) : 5792-5812.
  • 7Gullo C, Au M, Feng G, et al. The biology of Ku and its potential oncogenic role in cancer [J]. Biochim Biophys Acta, 2006, 1765(2) :223-234.
  • 8Paddison P J, Caudy A A, Bemstein E, et al. Short hairpin RNAs (shRNAs) induce sequence-specific silencing in mammalian cells [J]. Genes Dev, 2002, 16(8) :948-958.
  • 9Hsu H L, Gilley D, Galande S A, et al. Ku acts in a unique way at the mammalian telomere to prevent end joining [J]. Genes Dev, 2000, 14(22) :2807-2812.
  • 10Bailey S M, Brenneman M A, Halbrook J, et al. The kinase activity of DNA-PK is required to protect mammalian telomeres [J]. DNA Repair (Amst), 2004,3(3) :225-233.

引证文献4

二级引证文献15

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