中国医学创新
中國醫學創新
중국의학창신
MEDICAL INNOVATION OF CHINA
2013年
36期
1-3,4
,共4页
张宇晴%徐优慧%黎文婷%邹学森%罗达亚%蔡定浩
張宇晴%徐優慧%黎文婷%鄒學森%囉達亞%蔡定浩
장우청%서우혜%려문정%추학삼%라체아%채정호
胃癌%胃泌素%丙谷胺%DNA甲基转移酶-1%基质金属蛋白酶-2%E-钙粘蛋白%甲基化
胃癌%胃泌素%丙穀胺%DNA甲基轉移酶-1%基質金屬蛋白酶-2%E-鈣粘蛋白%甲基化
위암%위비소%병곡알%DNA갑기전이매-1%기질금속단백매-2%E-개점단백%갑기화
Gastric Cancer%Gastrin%Proglumide%DNMT-1%MMP-2%E-Cadherin%Methylation
目的:通过检测胃泌素及丙谷胺干预下胃癌MKN45细胞DNMT-1基因表达与E-Cadherin和MMP-2基因甲基化变化的相关性。方法:胃癌细胞株分别在胃泌素和丙谷胺干预下分为空白组、胃泌素组、丙谷胺组和混合组,应用SYBR Green I Q-PCR检测各组DNMT-1基因表达水平;运用RQ-MSP法检测用亚硫酸氢盐修饰后的基因组DNA为模板的各组基因甲基化状态。结果:胃泌素组与空白组相比, DNMT-1表达明显增高,而丙谷胺组则表达明显减低(P<0.05);DNMT-1表达量与E-Cadherin甲基化变化存在明显相关性,而与MMP-2甲基化并无明显相关性。结论:胃泌素可促进DNMT-1表达,DNMT-1可能直接影响E-Cadherin甲基化,而其可能间接影响MMP-2表达模式。
目的:通過檢測胃泌素及丙穀胺榦預下胃癌MKN45細胞DNMT-1基因錶達與E-Cadherin和MMP-2基因甲基化變化的相關性。方法:胃癌細胞株分彆在胃泌素和丙穀胺榦預下分為空白組、胃泌素組、丙穀胺組和混閤組,應用SYBR Green I Q-PCR檢測各組DNMT-1基因錶達水平;運用RQ-MSP法檢測用亞硫痠氫鹽脩飾後的基因組DNA為模闆的各組基因甲基化狀態。結果:胃泌素組與空白組相比, DNMT-1錶達明顯增高,而丙穀胺組則錶達明顯減低(P<0.05);DNMT-1錶達量與E-Cadherin甲基化變化存在明顯相關性,而與MMP-2甲基化併無明顯相關性。結論:胃泌素可促進DNMT-1錶達,DNMT-1可能直接影響E-Cadherin甲基化,而其可能間接影響MMP-2錶達模式。
목적:통과검측위비소급병곡알간예하위암MKN45세포DNMT-1기인표체여E-Cadherin화MMP-2기인갑기화변화적상관성。방법:위암세포주분별재위비소화병곡알간예하분위공백조、위비소조、병곡알조화혼합조,응용SYBR Green I Q-PCR검측각조DNMT-1기인표체수평;운용RQ-MSP법검측용아류산경염수식후적기인조DNA위모판적각조기인갑기화상태。결과:위비소조여공백조상비, DNMT-1표체명현증고,이병곡알조칙표체명현감저(P<0.05);DNMT-1표체량여E-Cadherin갑기화변화존재명현상관성,이여MMP-2갑기화병무명현상관성。결론:위비소가촉진DNMT-1표체,DNMT-1가능직접영향E-Cadherin갑기화,이기가능간접영향MMP-2표체모식。
Objective:To study gastrin and its antagonist on the expression of DNMT-1 and MMP-2\E-Cadherin methylation in gastric cancer line MKN45 and evaluate their molecules relationship. Method:Separate gastrin and its antagonist’s effect on gastric cancer cells were divided into four groups:controlled group,gastrin group,proglumid group,and mixed group. SYBR GreenⅠQ-PCR method was used to detect expressions of DNMT-1 in all the cases. Genomic DNA modified by sodium bisulfite was used as a template. RQ-MSP detected the methylation status of the gene promoter of MMP-2\E-cadherin. Result:DNMT-1 expression in gastrin group increased significantly in comparison to those of the controlled group(P<0.05). However,DNMT-1 expression in proglumid group decreased significantly in comparison to those of controlled group(P<0.05). There was a significant positive correlation between the expression of DNMT-1 and E-Cadherin methylation,but no correlation between MMP-2 methylation and the expression of DNMT-1. Conclusion:Gastrin can promote DNMT-1 expression. The expression of DNMT-1 may directly influence E-Cadherin methylation,yet may indirectly influence the expression pattern of MMP-2.