Alvarez-Salas L M, Cullinan A E, Siwkowski A, Hampel A, DiPaolo J A
Laboratory of Biology, Division of Basic Sciences, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892-4255, USA.
Proc Natl Acad Sci U S A. 1998 Feb 3;95(3):1189-94. doi: 10.1073/pnas.95.3.1189.
HPV-16 E6 and E7 genes are required to efficiently immortalize a broad spectrum of cell types including cervical keratinocytes. Therefore, the E6/E7 genes can be considered relevant targets for anti-cancer therapy. We produced several engineered hairpin (HP) ribozymes to specifically disrupt HPV-16 E6/E7 mRNA. After extensive biochemical characterization, one anti-E6 HP ribozyme (R434) was selected for in vivo testing because of its superior catalytic capabilities. When expressed in cis, R434 efficiently inhibited E6 in vitro translation. Cis-expression of the HP ribozyme with HPV-16 E6/E7 genes in normal human keratinocytes reduced the growth rate and prevented immortalization. RNA analysis by reverse transcription-PCR showed that E6/E7 transcripts were cleaved in post-transfected cells and virtually were eliminated after long term expression. Of interest, an inactive version of the HP also was able to significantly affect the immortalizing ability of E6/E7, probably through passive hybridization. The combination of passive and cleaving antisense RNA therefore is established as an effective inhibitor of HPV-16 E6/E7 immortalization.
HPV - 16 E6和E7基因对于有效永生化包括宫颈角质形成细胞在内的多种细胞类型是必需的。因此,E6/E7基因可被视为抗癌治疗的相关靶点。我们制备了几种工程化发夹(HP)核酶,以特异性破坏HPV - 16 E6/E7 mRNA。经过广泛的生化特性分析,由于其卓越的催化能力,选择了一种抗E6 HP核酶(R434)进行体内测试。当顺式表达时,R434在体外有效抑制E6的翻译。在正常人角质形成细胞中,HP核酶与HPV - 16 E6/E7基因的顺式表达降低了生长速率并阻止了永生化。通过逆转录 - PCR进行的RNA分析表明,E6/E7转录本在转染后细胞中被切割,长期表达后几乎被消除。有趣的是,HP的无活性版本也能够显著影响E6/E7的永生化能力,可能是通过被动杂交。因此,被动和切割反义RNA的组合被确立为HPV - 16 E6/E7永生化的有效抑制剂。