期刊文献+

维泰醇和紫杉醇抗肿瘤转移作用比较 被引量:7

Comparison of the anti-metastasis effect of alternol and paclitaxel
下载PDF
导出
摘要 目的观察维泰醇和紫杉醇对肿瘤细胞体外迁移能力以及血管内皮细胞管腔形成能力的影响,对它们的抗肿瘤转移能力进行比较,以证实维泰醇的抗肿瘤血管新生及抗肿瘤转移作用。方法采用SRB法,划痕试验,明胶酶谱法、ELISA、AO/EB染色法以及管腔样结构形成试验等方法观察比较维泰醇与紫杉醇的抗肿瘤转移能力。结果维泰醇对黑色素瘤细胞(B16F1)生长抑制率和致死率低于紫杉醇,维泰醇对黑色素瘤细胞迁移、MMP-2表达和对血管内皮细胞(ECV304)管腔形成的抑制能力略低于紫杉醇。结论维泰醇具有较强的抗肿瘤转移活性,虽然其抗转移能力弱于紫杉醇,但其低细胞毒特性依然有望成为新的抗肿瘤转移的药物。 To evaluate the anti-metastasis effect and the inhibition of the tube-like structure formation of human umbilical vein endothelial cells of alternol and paclitaxel.Methods SRB assay,scratch wound assay,gelatin zymography,ELISA methods,AO/EB assays and tube-like structure formation test were used to observe and compare the antitumor and antimetastasis ability. Results Alternol against melanoma cell growth inhibition rate and mortality rate were lower than paclitaxel,Alternol against melanoma cell migration,MMP-2 expression and the ability of inhibiting acknowledged formation slightly lower than paclitaxel.Results Taken together,the data suggested that alternol and paclitaxel have strong anti-metastasis activities.Alternol will be expected to become a novel,effective and low cytotoxic drug in the treatment of cancer.
出处 《中国药理学通报》 CAS CSCD 北大核心 2011年第8期1111-1115,共5页 Chinese Pharmacological Bulletin
基金 科技部重大新药创制科技重大专项研究资助项目(No2009ZX09103-141)
关键词 维泰醇 紫杉醇 转移 B16F1细胞 ECV304细胞 凋亡 管腔样结构 alternol paclitaxel metastasis B16F1 cells ECV304 cells apoptosis tube-like structure formation
  • 相关文献

参考文献4

二级参考文献28

  • 1杜钢军,林海红,许启泰,王敏伟,杨义明.反应停的抗新生血管形成及抗肿瘤作用研究[J].中国药理学通报,2005,21(4):471-474. 被引量:20
  • 2Wang G L, Semenza G L. General involvement of hypoxia-inducible factor 1 in transcriptional response to hypoxia[ J]. Proc Natl Acad Sci USA,1993,90(9) :4304 -8. 被引量:1
  • 3Semenza G L. Hydroxylation of HIF-1 : oxygen sensing at the molecular level [ J ]. Physiology ( Bethesda ) ,2004,19 : 176 - 82. 被引量:1
  • 4Kaelin W G. Proline hydroxylation and gene expression [ J ]. Annu Rev Biochem ,2005,74 : 115 - 28. 被引量:1
  • 5Bruick R K, McKnight S L. A conserved family of prolyl-4-hydroxylases that modify HIF [ J ]. Science, 2001,294 ( 5545 ) : 1337 - 40. 被引量:1
  • 6Amina A Q, Aleksmader S P. A computational model of intracellular oxygen sensing by hypoxia-inducible factor HIF-1 a [ J ]. J Cell Sci,2006,119 ( 16 ) :3467 - 80. 被引量:1
  • 7Stiehl D P, Jelkmann W,Wenger R H,et al. Normoxic induction of the hypoxia-inducible factor 1 alpha byinsulin and interleukin-1 beta involves the phosphatidylinositol 3-kinase pathway [ J ]. FEBS Lett. 2002,512 ( 1-3 ) : 157 - 62. 被引量:1
  • 8Nakayama K, Frew I J, Hagensen M, et al. Siah2 regulates stability of prolylhydroxylases, controls HIF1 alpha abundance, and modulates physiological responses to hypoxia [J]. Cell, 2004,117 ( 7 ) : 941 - 52. 被引量:1
  • 9Li Z,Wang D, Messing E M,et al. VHL protein-interacting deubiquitinating enzyme 2 eubiquitinates and stabilizes HIF-1 alpha [ J ]. EMBO Rep,2005,6(4) :373 - 8. 被引量:1
  • 10Li F, Sonveaux P, Rabbani Z N, et al. Regulation of HIF-lalpha stability through S-nitrosylation [ J ]. Mol Cell, 2007,26 ( 1 ) : 63 - 74. 被引量:1

共引文献16

同被引文献51

引证文献7

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