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Antitumor Activity of Synthetic Oligonucleotides with Sequences from cDNA Encoding Proteins of Mycobacterium bovis BCG

机译:牛分枝杆菌卡介苗cDNA编码蛋白序列的合成寡核苷酸的抗肿瘤活性

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摘要

Thirteen kinds of 45‐mer or 30‐mer synthetic oligonucleotides with sequences randomly selected from the cDNA encoding three kinds of protein of Mycobacterium bovis BCG were tested for their antitumor activity in a murine tumor system. Six out of the 13 single‐stranded oligonucleotides which contained one or more hexameric palindromic sequences showed strong antitumor activity while the others without palindromic structure did not. Namely, repeated intralesional injections of 100 μg of the 6 oligonucleotides caused regression of the established tumor but the other 7 were ineffective. When tumor cells were mixed with 100 μg of an effective oligonucleotide and injected into mice, tumor growth was markedly suppressed. These results suggested that palindromic structure is essential for the antitumor activity of the synthetic oligonucleotides.
机译:测试了13种45-mer或30-mer合成寡核苷酸,它们从编码牛分枝杆菌BCG三种蛋白质的cDNA中随机选择的序列在鼠肿瘤系统中的抗肿瘤活性。在包含一个或多个六聚体回文序列的13个单链寡核苷酸中,有六个显示出强大的抗肿瘤活性,而其他没有回文结构的寡核苷酸则没有。即,病灶内重复注射100μg的6种寡核苷酸导致已建立的肿瘤消退,而其他7种无效。当将肿瘤细胞与100μg有效寡核苷酸混合并注射到小鼠中时,肿瘤生长被显着抑制。这些结果表明回文结构对于合成寡核苷酸的抗肿瘤活性是必不可少的。

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