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c-ets-2、c-myc、N-ras三个癌基因联合反义RNA对肝癌细胞恶性表型的逆转 被引量:14

REVEERSALOF MALiGNANT PHENOTYPE OF HUMAN HEPATOMA CELLS BY ANTISNSE c-ets-2,c-myc and N-raS
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摘要 作者构建了一个能表达c-ets-2、c-myc及N-ras三个癌基因联合反义RNA的重组逆转录病毒载体,经病毒包装细胞PA317包装成假型逆转录病毒,利用此病毒成功地感染了人肝癌细胞株SMMC-7721,经G418筛选得到G418抗性细胞,基因组DNA杂交结果表明重组病毒稳定地整合入7721细胞基因组中。RNA杂交结果表明转化细胞中有较高水平的联合反义RNA表达。初步结果表明,反义RNA使7721细胞生长速率下降约70%,软琼脂集落形成能力及裸鼠致瘤能力显著下降。这一结果表明,针对多个癌基因的联合反义RNA可能给肿瘤基因治疗提供新的途径,有进一步探索的价值。 Abstract A recombinant retroviral vector was constructed which expressed antisense RNA of c-ets-2,c -myc and N-ras.The pseudotype virus was packaec and rescued by transfection in PA317 cells and used to infect human hepatoma cell line SMMC-7721.After selection with G418,resistant colonies were obtained. Stable integration of retrovirus in infectants was shown bv Southernhybridization of genomic DNA and the presence of antisense RNA was detected by RNA dot blot hybribization. It was demonstrated that the antisense RNAs did inhibit the growth of humanSMMC-7721 hepatoma cells.The ability to form colony in soft agar and tumorigenicity in nudemicr of SMMC-7721 were significantly suppressed by the antisense RNAs. The result implicatesthe potential value in future cancer gene therapy.
出处 《中华肿瘤杂志》 CSCD 北大核心 1994年第4期243-246,共4页 Chinese Journal of Oncology
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参考文献3

  • 1叶昕,中国科学.B,1991年,2卷,174页
  • 2田勇泉,分子生物学方法,1990年
  • 3鄂征,组织培养技术(第2版),1988年

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