期刊文献+

索拉非尼联合顺铂抑制卵巢癌H08910细胞生长的体外研究

The in vitro study on sorafenib combined with cisplatin for ovarian cancer cell H08910 growth inhibition
下载PDF
导出
摘要 目的对索拉非尼联合顺铂抑制卵巢癌H08910细胞生长进行体外研究。方法探讨索拉非尼、顺铂单用以及索拉非尼与顺铂联合应用对卵巢癌H08910细胞增殖的抑制率、细胞凋亡率、细胞周期影响。检测细胞增殖的抑制率采用四甲基偶氮唑蓝方法,检测细胞凋亡率、细胞周期应用流式细胞仪。结果联合用药组对卵巢癌H0-8910细胞增殖抑制率明显高于单独用药组,两者能够诱导细胞凋亡及阻滞细胞周期,在联合应用时表现出协同作用趋势。结论索拉非尼能够将患者对化疗药物的敏感性提高,降低化疗药物应用剂量及毒副作用,可能成为化疗药物良好辅助用药。 【Objective】To make an in vitro study on sorafenib combined with cisplatin for ovarian cancer cell H08910 growth inhibition.【Methods】 We studied on the effect of inhibition rate of ovarian cancer cell H08910 proliferation,the rate of apoptosis and cell cycle when used sorafenib or cisplatin alone,and Sorafenib combined with cisplatin.We used tetramethyl azo blue method to detect the inhibition rate of cell proliferation and flow cytometry to detect the rates of apoptosis and cell cycle.【Resluts】 The combined treatment group was significantly higher than simplex treatment group on inhibition rate of ovarian cancer cell H08910 proliferation.They can induce apoptosis and block the cell cycle in both groups.It demonstrated the synergies trend in combined group.【Conclusion】 Sorafenib can increase the sensitivity to chemotherapy drugs of patients and reduce the dose of chemotherapy drugs and side effects.It may become a good assistant drug for chemotherapy.
作者 胡丁月 张爽
出处 《中国医学工程》 2012年第12期28-29,共2页 China Medical Engineering
关键词 索拉非尼 顺铂 卵巢癌H08910细胞 体外研究 Sorafenib Cisplatin ovarian cancer cell H08910 in vitro study
  • 相关文献

参考文献6

二级参考文献43

  • 1Robertson D M, Klein R, de Vos FL, et al. The isolation of polypeptides with FSH suppressing activity from bovine follicular fluid which are structurally different to inhibin [J]. Biochem Biophys Res Commun, 1987,149 (2) :744.
  • 2Ueno N, Ling N, Ying S Y, et al. Isolation and partial characterization of follistatin: a single-chain Mr 35,000 monomeric protein that inhibits the release of follicle-stimulating hormone [J]. Proc Natl Acad Sei USA, 1987,84 (23) : 8282.
  • 3Maguer-Satta V, Bartholin L, Jeanpierre S, et al. Regulation of human erythropoiesis by activin A, BMP2, and BMP4, members of the TGFbeta family [J]. Exp Cell Res,2003,282(2): 110.
  • 4Nakamura T, Hasegawa Y, SuginoK, et al. Follistatin inhibits actvin-induced diffrenciatian of rat follistatin grannulosa ceils in vitro [J]. Biochem Biophys Acta, 1992,1135:103.
  • 5Wakatsuki M, Shintani M, Abe M, et al. Immunoradiometric assay for follistatin: Serum Immunoreactive follistatin level in normal adult and pregnant women [ J]. J Clin Endocrinol Metab, 1996,81:630.
  • 6Liu Z H, Shintani Y, Sakamoto Y, et al. Effects of LHRH, FSH and activin A on follistatin secretion from cuhured rat anterior pituitary cells [J]. Endocrine J, 1996,43: 321.
  • 7Farrell W E, Clark AJL, Stewart M F, et al. Bromocriptine inhibits Proopiomelanocortin mRNA and ACTH precursor secretion in small cell lung cancer cell lines [ J]. J Clin Invest, 1992,90: 705.
  • 8[1]Wilhelm SM,Carter C,Tang L,et al.BAY 43-9006 exhibits broad spectrum oral antitumor activity and targets the RAF/MEK/ERK pathway and receptor tyrosine kinases involved in tumor progression and angiogenesis.Cancer Res.2004 Oct 1; 64 (19):7099-109.
  • 9[2]Strumberg D,Richly H,Hilger RA,et al.Phase Ⅰ clinical and pharmacokinetic study of the Novel Raf kinase and vascular endothelial growth factor receptor inhibitor BAY 43 -9006in patients with advanced refractory solid tumors.J Clin Oncol,2005,23 (5):965
  • 10[3]Ratain MJ,Eisen T,Stadler WM,et al.Final findings from a phase Ⅱ,placebo-controlled,randomized discontinuatoin trial (RDT) of Sorafenib (Bay 43-9006) in patients with advanced renal cell carcinoma (RCC).J Clin Oncol,2005,23 (16S):Abstract 4544

共引文献75

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