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反义RNA对人胃癌细胞生长抑制及恶性表型的阻断作用
引用本文:吕有勇,张青云,谢山海,李诤,李文梅,胥薇,徐宁志,崔建涛,李吉友,邓国仁.反义RNA对人胃癌细胞生长抑制及恶性表型的阻断作用[J].中国生物化学与分子生物学报,1994,10(4):451-456.
作者姓名:吕有勇  张青云  谢山海  李诤  李文梅  胥薇  徐宁志  崔建涛  李吉友  邓国仁
作者单位:北京市肿瘤防治研究所生化及分子生物学实验室
基金项目:国家“863”和北京市科委高技术实验室资助
摘    要:ras原癌基因的点突变是人胃癌发生发展的重要机理之一。利用能表达c-H-ras癌基因反义RNA的质粒,导入人胃癌细胞系BGC-823,研究了ras癌基因反义RNA对人胃癌细胞生长及恶性表型的作用,结果表明,c-H-ras反义RNA可引起BGC-823生长速率及形态的变化,在半固体培养基中细胞集落形成能力减弱,部分地抑制了BGC-823在裸鼠体内的致瘤性。c-H-ras反义RNA对其RNA的过量表达呈特异性抑制作用。

关 键 词:反义RNA  c-H-ras  癌基因  胃癌细胞  恶性表型  
收稿时间:1994-08-20

Inhibition of Growth Ability and Tumorigenicity of Human Gastric Carcinoma Cell Iine BGC-823 Expressing c-Ha-ras Antisense and Sense RNA
Lu,You-yong,Zhang,Qing-yun,Xie,Shan-hai,Li,Zheng,Li,Wen-mei,Xu,Wei,Xu,Ning-zhi,Cui,Jian-tao,Li,Ji-you,Deng,Guo-ren.Inhibition of Growth Ability and Tumorigenicity of Human Gastric Carcinoma Cell Iine BGC-823 Expressing c-Ha-ras Antisense and Sense RNA[J].Chinese Journal of Biochemistry and Molecular Biology,1994,10(4):451-456.
Authors:Lu  You-yong  Zhang  Qing-yun  Xie  Shan-hai  Li  Zheng  Li  Wen-mei  Xu  Wei  Xu  Ning-zhi  Cui  Jian-tao  Li  Ji-you  Deng  Guo-ren
Institution:(Deparrment of Biochemistry and Molecular Biology. Beijing institute for Cancer Research, Beijing 100034
Abstract:Our previous work showed that point mutation plays an important role in the activation of H-ras protooncogene. We have inserted first exon and its upstream 2. 0 kb fragment of c-Ha-ras into shuttle vector pZipneoSV (X). The constructs of pZipneo2.0S and pZipneo2. 0AS of H-ras expressed sense and antisense RNA, respectively. We have introduced the constructs of pZipneo S and AS which expressed c-Ha-ras sense and antisense RNA into BGC-823 cell line with retrovirus infection. The colonies of G418 resistant were analysed on morphology, growth ability in serum free medium or soft agar and tumorigenicity in nude mice. Our data demonstrated that the growth ability or colonies forming efficiency in soft agar and tumorigenicity in nude mice were inhibited by c-Ha-ras antisense RNA.
Keywords:Antisense RNA i c-H-ras  Oncogene  Gastric carcinoma  Malignant phenotype
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