郑州大学学报(医学版)
鄭州大學學報(醫學版)
정주대학학보(의학판)
JOURNAL OF ZHENGZHOU UNIVERSITY(MEDICAL SCIENCES)
2014年
1期
4-7,8
,共5页
唐悦%轩小燕%柳璐璐%李敏
唐悅%軒小燕%柳璐璐%李敏
당열%헌소연%류로로%리민
EC9706/cDDP细胞%耐药%谷胱甘肽S转移酶-π%RNA干扰
EC9706/cDDP細胞%耐藥%穀胱甘肽S轉移酶-π%RNA榦擾
EC9706/cDDP세포%내약%곡광감태S전이매-π%RNA간우
EC9706/cDDP cell%drug-resistant%glutathione S-transferase-π%RNA interfering
目的:观察沉默谷胱甘肽S转移酶-π( GST-π)基因的表达对食管鳞状细胞癌顺铂耐药细胞系EC9706/cDDP细胞耐药性的影响。方法:构建靶向GST-π基因的siRNA重组慢病毒GSTs1i、 GSTsi2和无义对照GSTsiC,转染EC9706/cDDP细胞。通过RT-PCR及Western blot法检测GSTsi1、GSTsi2和GSTsiC感染前后EC9706/cDDP细胞中GST-πmRNA和蛋白的表达;MTT法检测感染GSTsi2、GSTsiC与未感染的EC9706/cDDP细胞对顺铂敏感性的变化。结果:感染GSTsi1、GSTsi2后EC9706/cDDP细胞GST-πmRNA的表达下调(F=3.490,P<0.001),其蛋白表达也减弱。感染GSTsi2的EC9706/cDDP细胞对顺铂的耐药指数较感染GSTsiC和未感染的EC9706/cDDP细胞降低(F=50.510,P<0.001)。结论:沉默GST-π基因的表达可降低EC9706/cDDP细胞的顺铂耐药性。
目的:觀察沉默穀胱甘肽S轉移酶-π( GST-π)基因的錶達對食管鱗狀細胞癌順鉑耐藥細胞繫EC9706/cDDP細胞耐藥性的影響。方法:構建靶嚮GST-π基因的siRNA重組慢病毒GSTs1i、 GSTsi2和無義對照GSTsiC,轉染EC9706/cDDP細胞。通過RT-PCR及Western blot法檢測GSTsi1、GSTsi2和GSTsiC感染前後EC9706/cDDP細胞中GST-πmRNA和蛋白的錶達;MTT法檢測感染GSTsi2、GSTsiC與未感染的EC9706/cDDP細胞對順鉑敏感性的變化。結果:感染GSTsi1、GSTsi2後EC9706/cDDP細胞GST-πmRNA的錶達下調(F=3.490,P<0.001),其蛋白錶達也減弱。感染GSTsi2的EC9706/cDDP細胞對順鉑的耐藥指數較感染GSTsiC和未感染的EC9706/cDDP細胞降低(F=50.510,P<0.001)。結論:沉默GST-π基因的錶達可降低EC9706/cDDP細胞的順鉑耐藥性。
목적:관찰침묵곡광감태S전이매-π( GST-π)기인적표체대식관린상세포암순박내약세포계EC9706/cDDP세포내약성적영향。방법:구건파향GST-π기인적siRNA중조만병독GSTs1i、 GSTsi2화무의대조GSTsiC,전염EC9706/cDDP세포。통과RT-PCR급Western blot법검측GSTsi1、GSTsi2화GSTsiC감염전후EC9706/cDDP세포중GST-πmRNA화단백적표체;MTT법검측감염GSTsi2、GSTsiC여미감염적EC9706/cDDP세포대순박민감성적변화。결과:감염GSTsi1、GSTsi2후EC9706/cDDP세포GST-πmRNA적표체하조(F=3.490,P<0.001),기단백표체야감약。감염GSTsi2적EC9706/cDDP세포대순박적내약지수교감염GSTsiC화미감염적EC9706/cDDP세포강저(F=50.510,P<0.001)。결론:침묵GST-π기인적표체가강저EC9706/cDDP세포적순박내약성。
Aim:To observe the effects of silencing the expression of GST-πon the drug-resistance of esophageal car-cinoma cells.Methods:The lentivirus of siRNA targeting to GST-πwas constructed.EC9706/cDDP cells were infected by the lentivirus named GSTsi1,GSTsi2.The mRNA and protein expressions of GST-πbefore and after infection were measured by RT-PCR and Western blot.Cells were divided into four groups:cells infected with GSTsi2, GSTsiC, untreat-ed EC9706/cDDP and EC9706 .Drug sensitivity to cDDP was determined by MTT .Results:The expression level of GST-πmRNA in cells infected by GSTsi1 and GSTsi2 were lower than those in control cells (F=3.490,P<0.001),and the ex-pression of GST-πprotein was also decreased .Compared with untreated EC9706/cDDP and EC9706/cDDP infected by GSTsiC,the resistance index of EC9706/cDDP infected by GSTsi2 decreased(F=50.510,P<0.001).Conclusion: Si-lencing the expression of GST-πby RNAi can partly reverse the drug resistance of EC 9706/cDDP.