期刊文献+

miRNA-93在卵巢癌OVCAR3细胞的侵袭和迁移中的作用研究 被引量:4

Study on effect of miR-93 on invasion and migration of human ovarian cancer OVCAR3 cells
暂未订购
导出
摘要 目的:研究miR-93对卵巢癌细胞系OVCAR3侵袭及迁移能力的影响。方法:用miR-93的成熟模拟物过表达miR-93,用化学合成的特异性抑制物下调miR-93的表达。通过miRNA特异的定量PCR验证miR-93的过表达和抑制效率,采用MTT、软琼脂集落形成和Transwell侵袭实验分析miR-93表达对OVCAR3细胞增殖、侵袭及迁移能力的影响。结果:miR-93过表达后,OVCAR3细胞的侵袭和迁移能力显著增强(分别达3.82倍和2.56倍)。降低内源性miR-93的表达后,OVCAR3细胞的侵袭和迁移能力分别下降了66.57%和57.26%。结论:miR-93能明显促进卵巢癌OVCAR3细胞的侵袭和迁移。 Objective:To verify the effect of miR-93 on the invasive and migratory abil- ity of human ovarian cancer cell line OVCAR3. Methods: The expression of miR-93 in OVCAR3 cells was upregulated by mimics and downregulated by inhibitors. The expression levels of miR-93 were measured by miRNA specific Real-Time PCR. Cell proliferation was detec- ted with MTT assay and sofl-agar colony formation assay. Effects of miR-93 on cell invasion and migration were evaluated by transwell invasive and migratory assay. Results:Overexpression of miR-93 in OVCAR3 cells, the invasive and migratory abilities were increased by 3.82-fold and 2.56-fold respectively. On the contrary,inhibition of endogenous miR-93 in OVCAR3 cells, the migration and invasion of cells were reduced by 57.26% and 66.57% respectively in vitro. Conclusion:miR-93 plays an important role in promoting invasion and migration of human o- varian cancer cell line OVCAR3.
出处 《现代妇产科进展》 CSCD 2014年第9期681-684,共4页 Progress in Obstetrics and Gynecology
关键词 卵巢癌 侵袭 迁移 miR-93 Ovarian cancer Invasion Migration miR-93
  • 相关文献

参考文献21

  • 1Gupta GP, MassagueJ. Cancer metastasis:building a frame- work[J]. Cell ,2006,127(4) :679-695.
  • 2Bartel DP. MicroRNAs : genomics, biogenesis, mechanism, and function[J]. Ce11,2004,116(2) :281-297.
  • 3Yekta S, Shih IH, Bartel DP. MicroRNA-directed cleavage of HOXB8 mRNA[J].Science,21X)4,304(5670) :594-596.
  • 4Volinia S, Calin CA, Liu CG, et al. A microRNA expression signature of human solid tumors defines cancer gene targets [J]. Proc Natl Acad Sci,2006,103(7):2257-2261.
  • 5Ma L,Teruya-Feldstein J ,Weinberg RA. Tumour invasion and metastasis initiated by microRNA-10b in breast cancer [J]. Nature,2007,449 (7163) :682-688.
  • 6Tavazoie SF ,Alarcon C ,Massague J ,et al. Endogenous human microRNAs that suppress breast cancer metastasis [ J ]. Na- ture ,2008,451 (7175) : 147-152.
  • 7Valastyan S ,Reinhardt F,Weinherg RA,et al. A pleiotropieal- ly acting microRNA,miR-31 ,inhibits breast cancer metastasis [J]. Cell ,2009, 137(6) :1032-1046.
  • 8Iorio MV ,Visone R, Di I-eva G, et al. MicroRNA signatures in human ovarian cancer[J]. Cancer Res,2007,67(18) :8699- 707.
  • 9Corney DC,Flesken-Nikitin A,Godwin AK,et al. MicroRNA- 34b and MicroRNA-34c are targets of p53 and cooperate in control of cell proliferation and adhesion-independent growth [J]. J Cancer Res,2007,67(18) :8433-8438.
  • 10Anlur K,Nagaraja C,Zhifeng Y,et al. A link between mir- 1130 and FRAP1/Mtor in clear cell ovarian cancer[J]. Origi- nal Res,2010,24(2) :447-463.

同被引文献26

引证文献4

二级引证文献26

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