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作 者:蔡海东[1] 谯娱[2] 余飞[1] 袁雪宇[1] 孙明[1] 吕中伟[1]
机构地区:[1]同济大学附属第十人民医院核医学科,上海200072 [2]第二军医大学附属长海医院输血科,上海200439
出 处:《同济大学学报(医学版)》2009年第5期40-43,共4页Journal of Tongji University(Medical Science)
摘 要:目的探讨jetPEI-RGD介导的125I-(αV)ASODN体外对人HCC细胞生长抑制的影响。方法用125I标记整合素αV亚基的ASODN,以聚乙烯亚胺衍生物jetPEI-RGD为转运载体转染进入Hep G2细胞,MTT法检测复合物对Hep G2细胞生长的抑制率。结果jetPEI-RGD/125I-(αV)ASODN组的细胞抑制率与jetPEI-RGD/(αV)ASODN组比较,差异无统计学意义(P>0.05),与其余各实验对照组比较,细胞抑制率增高,差异具有统计学意义(P<0.001),且在一定的范围内抑制率与投药剂量呈正相关(r=0.879)。结论jetPEI-RGD介导的125I-(αV)ASODN能有效抑制Hep G2细胞的生长增殖。Objective To observe the inhibitive effect of ^125I - (otv ) ASODN mediated by jetPEI-RGD on human hepatic carcinoma cells in vitro. Methods αv antisense oligonucleotides labeled with ^125I were transfected into HepG2 cells by jetPEI-RGD, and the inhibitory rates of hepG2 cells were examined by using MTT method. Results There was no significant difference in the inhibitory rates between jetPEI-RGD/^25I - ( αv) ASODN group and jetPEI-RGD/ ( αv ) ASODN group ( P 〉 0.05 ). However, the inhibitory rates increased with statistically significant difference compared with those of the rest of experimental groups ( P 〈 0. 001 ). The cell inhibitory rates positively correlated with drug dose ( r = 0. 879 ) within a certain range. Conclusion ^125I - (αv) ASODN mediated by jetPEI-RGD can effectively inhibit the growth and proliferation of HepG2 ceils.
关 键 词:jetPEI-RGD 整合素αV亚基 ASODN 肝细胞肝肿瘤
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