MG132、顺铂联合用药对Caov-3细胞中NF-κB、VEGF表达的影响

顾光华, 张磊, 李彩霞

顾光华, 张磊, 李彩霞. MG132、顺铂联合用药对Caov-3细胞中NF-κB、VEGF表达的影响[J]. 实用临床医药杂志, 2010, (17): 22-25. DOI: 10.3969/j.issn.1672-2353.2010.17.007
引用本文: 顾光华, 张磊, 李彩霞. MG132、顺铂联合用药对Caov-3细胞中NF-κB、VEGF表达的影响[J]. 实用临床医药杂志, 2010, (17): 22-25. DOI: 10.3969/j.issn.1672-2353.2010.17.007
GU Guang-hua, ZHANG Lei, LI Cai-xia. Expressions of NF-κB and VEGF in Caov-3 cells after the administration of MG132 combined with DDP[J]. Journal of Clinical Medicine in Practice, 2010, (17): 22-25. DOI: 10.3969/j.issn.1672-2353.2010.17.007
Citation: GU Guang-hua, ZHANG Lei, LI Cai-xia. Expressions of NF-κB and VEGF in Caov-3 cells after the administration of MG132 combined with DDP[J]. Journal of Clinical Medicine in Practice, 2010, (17): 22-25. DOI: 10.3969/j.issn.1672-2353.2010.17.007

MG132、顺铂联合用药对Caov-3细胞中NF-κB、VEGF表达的影响

详细信息
  • 中图分类号: R737.31

Expressions of NF-κB and VEGF in Caov-3 cells after the administration of MG132 combined with DDP

  • 摘要: 目的 研究蛋白酶体抑制剂MG132与DDP联合用药前后卵巢癌细胞株Caov-3细胞内NF-κB、VEGF表达情况.方法 免疫组化SP法测定用药前后Caov-3细胞中NF-κB、VEGF的表达情况.结果 免疫组化结果显示MG132、DDP联合用药作用24 h后Caov-3细胞中NF-κB、VEGF表达均下调,与对照组、DDP组比较差异有显著性(P<0.01),联合用药组各组间两两比较差异有显著性(P<0.01).结论 MG132能通过抑制NF-κB活性诱导卵巢癌细胞Caov-3凋亡,抑制肿瘤血管生长.
  • 乐杰. 妇产科学 [M]. 北京:人民卫生出版社, 2008.278.
    Wu HJ, Zhang ZG. Ubiquitin-Proteasome pathway and its significance [J]. Journal of International Pathology and Clinical Medicine, 2006(1):7.doi: 10.3969/j.issn.1673-2588.2006.01.002.
    Inoue S, Nakase H, Matsuura M. The effect of proteasome inhibitor MG132 on experimental inflammatory bowel disease [J]. Clinical and Experimental Immunology, 2009(1):172.doi: 10.1111/j.1365-2249.2008.03872.x.
    Sen R, Baltimore D. Multiple nuclear factors interact with the immunoglobulin enhancer sequence [J]. Cell, 1986(5):705.doi: 10.1016/0092-8674(86)90346-6.
    Ishii Y, Waxman S, Germain D. Targeting the ubiquitin-proteasome pathway in cancer therapy [J]. Anti-cancer Agents in Medical Chemistry, 2007(3):359.doi: 10.2174/187152007780618180.
    Meiners S, Lauie M, Rother W. Ubiquitin-proteasome pathway as a new target for the prevention of restenosi [J]. Circulation, 2002(4):483.doi: 10.1161/hc0402.102951.
    Munshi A, Kurland JF, Nishnkawa T. Inhibition of constitutively activated nuclear factor-kappaB radiosensitizes human melanoma cells [J]. Molecular Cancer Therapeutics, 2004(8):985.
    Ferrara N, Henzel WJ. Pituitary follicular cells secrete a novel heparin-binding growth factor specific for vascular endothelial cells [J]. Biochemical and Biophysical Research Communications, 1989(2):851.doi: 10.1016/0006-291X(89)92678-8.
    Wong C, Wellman TL, Lounsbury KM. VEGF and HIF-1alpha expression are increased in advanced stages of epithelial ovarian cancer [J]. Gynecologic Oncology, 2003(3):513.doi: 10.1016/j.ygyno.2003.08.022.
    Byrne AT, Ross L, Holash J. Vascular endothelial growth factor-trap decreases tumor burden, inhibits ascites, and causes dramatic vascular remodeling in an ovarian cancer model [J]. Clinical Cancer Research, 2003, (15):5721.
    Xiong HQ, Abbruzzese JL, Lin E. NF-kappaB activity blockade impairs the angiogenic potential of human pancreatic cancer cells [J]. International Journal of Cancer, 2004(2):181.doi: 10.1002/ijc.11562.
    Yu HG, Zhong X, Yang YN. Increased expression of nuclear factor-kappaB (RelA) is correlated with tumor angiogenesis in human colorectal cancer [J]. International Journal of Colorectal Disease, 2004(1):18.doi: 10.1007/s00384-003-0494-z.
    Yoshida S, Ono M, Shono T. Involvement of interleukin-8, vascular endothelial growth factor, and basic fibroblast growth factor in tumor necrosis factor anlpha-dependent angiogenesis [J]. Molecular and Cellular Biology, 1997(7):4015.
    Huang S, Pettaway CA, Uehara H. Blockade of NF-kappaB activity in human prostate cancer cells is associated with suppression of angiogenesis, invasion, and metastasis [J]. Oncogene, 2001, (31):4188.
    Shibata A, Nagaya T, Imai T. Inhibition of NF-kappaB activity decreases the VEGF mRNA expression in MDA-MB-231 breast cancer cells [J]. Breast Cancer Research and Treatment, 2002(3):237.doi: 10.1023/A:1015872531675.
计量
  • 文章访问数:  240
  • HTML全文浏览量:  23
  • PDF下载量:  11
  • 被引次数: 0
出版历程
  • 发布日期:  2010-12-15

目录

    /

    返回文章
    返回
    x 关闭 永久关闭