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作 者:杨定成[1] 战洪生[1] 张礼和[1] 李通[1] 藏传兵 王来新 吕有勇[1]
机构地区:[1]北京医科第一医院外科,北京医科大学天然及仿生药物国家重点实验室,北京市肿瘤防治研究所生化室
出 处:《北京医科大学学报》1995年第5期353-355,369,共4页Journal of Peking University(Health Sciences)
基 金:国家自然科学基金及国家重点实验室资助课题
摘 要:应用突变c-Ha-ras质粒DNA转化小鼠C3H10T1/2纤维细胞,发现细胞获得恶性表型。本文合成了反义DNA(oligo),它与c-Ha-ras基因前4个密码子及其上游正链序列互补;并发现oligo可有效地抑制恶性转化细胞内c-Ha-ras基因表达、细胞在软琼脂中集落形成以及细胞在裸鼠体内的致瘤作用。补骨脂素修饰oligo后,其生物学活性增强。n this study ,the mice fibroblast cell line-C3H10T1/2 was transformed with mutated c-Ha-ras plasmid DNA.The transformed C3H10T1/2 cell obtained the malignant phenotype. The antisense c-Ha-ras DNA (oligo) was syn-thesized in this study. The oligo was complementary to the single positive strand of the first four codons and the upstream sequence of c-Ha-ras gene.We found that the expression of activated c-Ha-ras oncogene,foci formation in soft agar and tumorigenicity in nude mice of the transformed C3H10T1/2 cells could be effectively inhibited by oli- go.When psoralen group was covalently linked to the 5’-end of the oligo,the biological effect of oligo was en-banced.
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