Wickstrom E, Bacon T A, Wickstrom E L
Department of Chemistry, University of South Florida, Tampa 33620.
Cancer Res. 1992 Dec 15;52(24):6741-5.
In transgenic mice bearing a murine immunoglobulin enhancer/c-myc fusion transgene (Emu-myc), it was found that antisense DNA methylphosphonates targeted against c-myc mRNA inhibited production of c-MYC protein in peripheral lymphocytes. The decrease in protein was measured 3-4 h after i.v. administration of a 300-nmol dose. c-MYC was detected by immunofluorescence of fixed cells stained with an anti-c-MYC antiserum. In addition, DNA methylphosphonates did not induce acute toxicity following i.v. administration of a 300-nmol dose. An identically administered scrambled sequence oligomer did not decrease c-MYC protein or induce toxicity. Finally, recovery of DNA methylphosphonates from the blood plasma of treated mice indicated that the oligomers remained intact up to 3 h, while their concentrations decreased rapidly for the first h, then slowly decreased over the next 2 h. This is the first demonstration of sequence-specific antisense DNA methylphosphonate inhibition of gene expression in the bloodstream of an animal model.
在携带鼠免疫球蛋白增强子/c-myc融合转基因(Emu-myc)的转基因小鼠中,发现针对c-myc mRNA的反义DNA甲基膦酸酯可抑制外周淋巴细胞中c-MYC蛋白的产生。静脉注射300 nmol剂量后3-4小时测量蛋白减少情况。用抗c-MYC抗血清对固定细胞进行免疫荧光检测c-MYC。此外,静脉注射300 nmol剂量的DNA甲基膦酸酯后未诱导急性毒性。同样给药的乱序序列寡聚物未降低c-MYC蛋白或诱导毒性。最后,从处理过的小鼠血浆中回收DNA甲基膦酸酯表明,寡聚物在长达3小时内保持完整,而其浓度在第一个小时迅速下降,然后在接下来的2小时内缓慢下降。这是首次在动物模型的血流中证明序列特异性反义DNA甲基膦酸酯对基因表达的抑制作用。