Budryk M, Wilczyńska U, Szary J, Szala S
Department of Molecular Biology, Centre of Oncology-Maria Skłodowska-Curie Memorial Institute, Gliwice, Poland.
Acta Biochim Pol. 2000;47(2):385-91.
We investigated the feasibility of transferring naked plasmid DNA containing a therapeutic gene (IL-12) into mice harboring growing Renca tumors. We found that naked DNA transferred into growing Renca and B16(F10) tumors gives higher expression level of reporter gene than complexes of DNA with DDAB/DOPE or DC-Chol/DOPE. Transfer of naked DNA carrying the IL-12 gene into growing Renca tumors causes a distinct therapeutic effect that depends on the time span between inoculation of mice with cancer cells and the beginning of the therapy. Therapy started on day 3 resulted in total cure (100%) of mice.
我们研究了将携带治疗性基因(白细胞介素-12)的裸质粒DNA导入患有正在生长的Renca肿瘤的小鼠体内的可行性。我们发现,导入正在生长的Renca和B16(F10)肿瘤中的裸DNA所产生的报告基因表达水平高于DNA与二甲基二烯丙基氯化铵/二油酰磷脂酰乙醇胺(DDAB/DOPE)或二氯胆固醇/二油酰磷脂酰乙醇胺(DC-Chol/DOPE)形成的复合物。将携带白细胞介素-12基因的裸DNA导入正在生长的Renca肿瘤会产生显著的治疗效果,这取决于给小鼠接种癌细胞与开始治疗之间的时间间隔。在第3天开始治疗可使小鼠完全治愈(100%)。