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甲基化转移酶抑制剂zebularine对人胃癌SGC-7901细胞株上皮性钙黏附蛋白基因表达的影响 被引量:1

The effect of zebularine on E-cadherin mRNA expression in SGC-7901 cell line
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摘要 目的 观察甲基化转移酶抑制剂zebularine对人胃癌SGC-7901细胞株增殖、迁移和上皮性钙黏附蛋白(E-cadherin)基因表达的影响.方法 采用噻唑蓝(MTT)法和划痕实验检测zebularine对人胃癌SGC-7901细胞株的抑制率及其细胞迁移率的影响,采用实时定量聚合酶链反应(Real-time PCR)检测作用前后E-cadherin基因表达的变化.结果 (1)终质量浓度100 μmol/L的zebularine作用24h能显著抑制SGC-7901细胞株的增殖率和迁移率.MTT法对照组吸光度值为0.50±0.01,实验组为0.45 ±0.02(P <0.05);对照组划痕愈合率为(47.45±10.05)%,实验组为(88.23±5.45)% (P <0.05).(2) zebularine作用24h能显著增加E-cadherin mRNA的表达,对照组相对表达量为1.02±0.10,实验组为4.25±0.56(P <0.05).结论 甲基化转移酶抑制剂zebularine可以有效抑制SGC-7901细胞株的增殖和迁移,并提高抑癌基因E-cadherin mRNA的表达. Objective To study the effect of DNA methylation inhibitor zebularine on the proliferation,migration and the expression of E-cadherin in human gastric carcinoma cell line SGC-7901.Methods Methyl thiazol tetrazolium (MTT) and the wound healing assays were used to evaluate the effect of zebularine on proliferation and migration of SGC-7901 cells.The mRNA expression of E-cadherin was detected by real-time quantitative polymerase chain reaction (Real-time PCR).Results (1) zebularine at a final concentration of 100 μmol/L significantly inhibited the proliferation (0.50 ± 0.01 vs.0.45 ± 0.02) and migration capacity [(47.45 ± 10.05) % vs.(88.23 ± 5.45) %] of SGC-7901 cells after 24 h (P 〈 0.05).(2) Zebularine significantly increased the mRNA expression of E-cadherin in SGC-7901 cells after 24 h (1.02 ± 0.10 vs.4.25 ± 0.56,P 〈 0.05).Conclusion DNA methylation inhibitor zebularine can effectively decrease the proliferation and migration of SGC-7901 cells,and significantlv increase the mRNA expression of E-cadherin at a final concentration of 100 μmol/L after 24 h.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2015年第3期470-472,共3页 Chinese Journal of Experimental Surgery
关键词 ZEBULARINE 上皮性钙黏附蛋白 胃癌 Zebularine E - cadherin Gastric carcinoma
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  • 1戴观荣,景洪标,邓鉴文.胃癌中脆性组氨酸三联体基因的甲基化和表达及其意义[J].中华实验外科杂志,2006,23(5):594-596. 被引量:7
  • 2Vogelauer M,Wu J,Suka N,et al.Global histone acetylation and deacetylation inyeast[J].Nature,2000,408(6811):495-498
  • 3Wajed SA,Laird PW,DeMeester TR.DNA methylaion:an alternative pathway to caner[J].Ann Surg,2001,234(1):10-20
  • 4Ou JN,Torrisani J,Unterberger A,et al.Histone deacetylase inhibitor Trichostatin A induces global and gene-specific DNA demethylation in human cancer cell lines[J].Biochem Pharmacol,2007,73:1297-1307
  • 5Jones PA.DNA methylation errors and cancer J[J].Cancer Res,1996,56(11):2465-2467
  • 6房静远.表型遗传修饰与肿瘤[M].上海:上海科技出版社,2002
  • 7Xu XL,Yu J,Zhang HY,et al.Methylation profile of the promoter CpG island of 31 genes that may contribute tocolorectal carcinogenesis[J].World J Gastroenterol,2004,10(23):3441-3454
  • 8Reinhold WC,Reimers MA,Lorenzi P,et al.Multifactorial regulation of E-cadherin expression:an integrative study[J].Mol Cancer Ther,2010,9(1):1-16.
  • 9van Roy F,Berx G.The cell-cell adhesion molecule E-cadherin[J].Cell Mol Life Sci,2008,65(23):3756-3788.
  • 10Saydam O,Shen Y,Würdinger T,et al.Downregulated microRNA-200a in meningiomas promotes tumor growth by reducing E-cadherin and activating the Wnt/beta-catenin signaling pathway[J].Mol Cell Biol,2009,29(21):5923-5940.

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