Citro G, Ginobbi P, Szczylik C
Laboratory of Experimental Chemotherapy, Regina Elena Institute for Cancer Research, Rome, Italy.
Cytotechnology. 1993;11 Suppl 1:S30-4.
The lack of efficient and specific delivery to target cells still limits the potential application of antisense oligodeoxynucleotides as therapeutic agents in cancer disease. We have covalently linked a polylysine chain (10,000-20,000 mw) to compounds as folic acid, retinoic acid, transferrin, insulin and estradiol, to deliver c-myb antisense oligonucleotide into tumor cells. Using these complexes as carriers for the oligodeoxynucleotides can be achieved an increase in their uptake into target cells through a natural endocytosis pathway.
缺乏对靶细胞高效且特异的递送方式,仍然限制了反义寡脱氧核苷酸作为治疗剂在癌症疾病中的潜在应用。我们已将一条聚赖氨酸链(分子量10,000 - 20,000)共价连接到叶酸、视黄酸、转铁蛋白、胰岛素和雌二醇等化合物上,以将c - myb反义寡核苷酸递送至肿瘤细胞。使用这些复合物作为寡脱氧核苷酸的载体,可通过天然内吞途径实现其对靶细胞摄取的增加。