期刊文献+

转化生长因子β_1对子宫内膜癌细胞系Ishikawa体外增殖、细胞周期、凋亡的影响 被引量:4

Effect of TGF-β_1 in Proliferation,Cell Cycle and Apoptosis of the Endometrial Carcinoma Cell Line Ishikawa in vitro
暂未订购
导出
摘要 目的探讨转化生长因子β(1TGF-β1)对子宫内膜癌细胞系Ishikawa体外增殖、细胞周期及凋亡的影响。方法用MTT法检测细胞增殖水平,通过流式细胞术观察细胞周期和凋亡的变化。结果TGF-β1以时间依赖方式明显抑制Ishikawa细胞的生长(P<0.05),各浓度间差异显著,随浓度增高抑制更加显著(P<0.05)。TGF-β1促进Ishikawa细胞凋亡,细胞凋亡百分比随时间及浓度的增加而增长;TGF-β1阻滞细胞停滞于G1期,S期的比例显著降低。结论TGF-β1能抑制人子宫内膜癌Ishikawa细胞的增殖,促进细胞凋亡,阻滞细胞周期。 Objective To investigate the effect of TGF-β1 in proliferation,cell cycle and apoptosis of the endometrial carcinoma cell line Ishikawa in vitro.Methods MTT assay was used to measure the proliferation of cells at different time and different concentration.Flow cytometry was employed to investigate cell apoptosis and cell cycle.Results TGF-β1 inhibited the proliferation of Ishikawa cell,and it had significant difference at different concentration of TGF-β1(P〈 0.05).TGF-β1 could promote the apoptosis of Ishikawa cell.TGF-β1 apparently blocked the Ishikawa cell at G1 phase.Conclusion TGF-β1 may partly inhibit the proliferation of Ishikawa cell,promote its apoptosis and block the Ishikawa cell at G1 phase.
出处 《中国医科大学学报》 CAS CSCD 北大核心 2010年第4期255-257,共3页 Journal of China Medical University
基金 辽宁省教育厅科学研究计划项目(05L474)
关键词 转化生长因子β1 人子宫内膜癌细胞 ISHIKAWA 凋亡 细胞周期 TGF-β1 human endometrial carcinoma cell Ishikawa apoptosis cell phase
  • 相关文献

参考文献9

  • 1Lasky JA, Ortiz LA. Antifibrotic therapy for the treatment of pulmonary fibrosis[ J ]. Am J Med Sci, 2001,322(4) : 213-222.
  • 2Barnard JA, Lyins RM, Moses HI. The cell biology of transforming growth factor beta [J]. Biochem Biophys Acta, 1990,1032 ( 1 ) :79- 87.
  • 3Inan S,Vatansever S,Celik-Ozenci C,et al. Immunolocalizations of VEGR, its receptors fit-1, KDR and TGF-beta's in epithelial ovarian tumors[ J ].Histol Histopathol, 2006,21 (10) : 1055-1064.
  • 4Shigeoka Y, Igishi T, Matsumoto S, et al. Sulindac sulfide and caffeic acid phenethyl ester suppress the motility of lung adenocarcinoma cells promoted by transforming growth factor-beta through Akt inhibi- tion[J]. Cancer Res Clin Oncol,2004, 130(3 ) : 146-152.
  • 5Berger DH,Ko CY,Spain DA. Intestinal transformation results in transforming growth factor-beta-dependent alteration in tumor cell- cell matrix interactions[ J ]. Surgery, 2003,133 (5) : 568-579.
  • 6Parekh TV, Gama P, Wen X, et al. Transforming growth factor beta signaling is disabled early in human endometrial carcinogenesis concomitant with loss of growth inhibition [J]. Cancer Res,2002,62 (10) : 2778-2790.
  • 7Carcamo J, Zentella A, Massague J. Disruption of transforming growth factor beta signaling by a mutation that prevents transphosphorylation within the receptor complex[J]. Mol Cell Biol, 1995,15(3):1573- 1581.
  • 8Maliekal TT, Antony ML, Nair A, et al. Loss of expression, and mutations of Smad 2 and smad 4 in human cervical cancer[ J ]. Oncogene, 2003,22(3) :4889-4897.
  • 9Jin X, Gossett DR, Wang S, et al. Inhibition of AKT survival pathway by a small molecule inhibitor in human endometrial cancer cells[J]. Br J Cancer,2004,91 (10) : 1808-1812.

同被引文献37

  • 1曹泽毅.中华妇产科学[M].2版.北京:人民卫生出版社,2004:2163-2169.
  • 2Wildemeersch D, Janssens D, Pylyser K, et al. Management of patients with non-atypical and atypical endometrial hyperplasia with a levonorgestrel-releasing intrauterine system: long-term follow-up[J]. Maturitas, 2007, 57(2): 210-3.
  • 3Higham JM, O' Brien PM, Shaw RW. Assessment of menstrual blood loss using a pictorial chart[J]. Br J Obstet Gynecol, 1990, 97 (8): 734-9.
  • 4许良中.乳腺病删学[M].上海:上海医科大学出版社,1999:332-43.
  • 5Xiao BL, Zhou LY, Zhang XL, et al. Pharmacokinetic and pharmacodynamic studies of levonorgestrel-releasing intrauterine device[J]. Contraception, 1990, 41 (4): 353-62.
  • 6Beatty MN, Blumenthal PD. The levonorgestrel-releasing in- trauterine system: Safety, efficacy, and patient acceptability [J]. Ther Clin Risk Manag, 2009, 5(3): 561-74.
  • 7Gomes MK, Rosa-e-Silva JC, Garcia SB, et al. Effects of the levonorgestrel-releasing intrauterine system on cell proliferation, Fas expression and steroid receptors in endometriosis lesions and normal endometrium[J]. Hum Reprod, 2008, 24(11 ): 2736-45.
  • 8Bergeron C, Ferenczy A, Shyamala G. Distribution of estrogen receptors in various cell types of normal, hyperplastic, and neoplastic human endometrial tissues [J]. Lab Invest, 1988, 58(3): 338-45.
  • 9Critchley HO, Wang H, Kelly RW, et al. Progestin receptor isofonns and prostaglandin dehydrogenase in the endometrium of women using a levonorgestrel-releasing intrauterine system [J]. Hum Reprod, 1998, 13(5): 1210-7.
  • 10Zhu P, Liu X, Luo H, et al. The effect of a levonorgestrel-releasing intrauterine device on human endometrial oestrogen and progesterone receptors after one year of use[J]. Hum Reprod, 1999, 14(4): 970-5.

引证文献4

二级引证文献42

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