Steele C, Cowsert L M, Shillitoe E J
Department of Microbiology, University of Texas Dental Branch, Houston 77225.
Cancer Res. 1993 May 15;53(10 Suppl):2330-7.
DNA of human papillomavirus type 18 is present in several human cancer cell lines that were derived from oral or cervical tumors, and it is known that several features of the transformed phenotype can be inhibited by expression of antisense RNA to human papillomavirus (HPV). The present study was performed to find out whether antisense oligonucleotides were also inhibitory. Synthetic oligonucleotides were made that were complementary to regions of the start codons of the E6 and E7 genes of HPV-18. These were added to cultures of the oral cancer cell line 1483 and the cervical cancer cell line C4-1, each of which contain DNA of HPV-18. As controls we used the oral cancer cell line 183 and the monkey kidney cell line Vero, which do not contain HPV. Anti-E6 and anti-E7 oligonucleotides, in concentrations between 1 and 5 microM, significantly inhibited the growth of the 1483 and C4-1 cells, but not the 183 or Vero cell lines. Treatment of the 1483 cells with a combination of 2.5 microM of each of the antisense oligonucleotides was a more effective inhibitor than 5 microM of either one used alone. Antisense oligonucleotides had no effect on the ability of 1483 cells to form foci in soft agar, nor on their plating efficiency or serum requirements. Microscopic examination of 1483 cells showed that the antisense E7 oligonucleotide produced cell-rounding, detachment from the surface of the culture flask, and cell death, while the antisense E6 oligonucleotide had none of these effects. Random-sequence oligonucleotides had no effects of any type on any cells that were growing in culture. However, if random-sequence oligonucleotides were added to cells at the time they were passed to a new culture vessel, they produced severe nonspecific toxic effects. These results show that the use of synthetic oligonucleotides is an effective way of producing antisense-mediated changes in the behavior of human cancer cells that contain DNA of HPV-18.
18型人乳头瘤病毒的DNA存在于多种源自口腔或宫颈肿瘤的人类癌细胞系中,并且已知通过表达针对人乳头瘤病毒(HPV)的反义RNA可以抑制转化表型的几个特征。本研究旨在确定反义寡核苷酸是否也具有抑制作用。合成了与HPV - 18的E6和E7基因起始密码子区域互补的寡核苷酸。将这些寡核苷酸添加到口腔癌细胞系1483和宫颈癌细胞系C4 - 1的培养物中,这两种细胞系均含有HPV - 18的DNA。作为对照,我们使用了不含HPV的口腔癌细胞系183和猴肾细胞系Vero。浓度在1至5微摩尔之间的抗E6和抗E7寡核苷酸显著抑制了1483和C4 - 1细胞的生长,但对183或Vero细胞系没有影响。用每种反义寡核苷酸2.5微摩尔的组合处理1483细胞比单独使用5微摩尔的任何一种都更有效。反义寡核苷酸对1483细胞在软琼脂中形成集落的能力、其接种效率或血清需求没有影响。对1483细胞的显微镜检查表明,反义E7寡核苷酸导致细胞变圆、从培养瓶表面脱离并细胞死亡,而反义E6寡核苷酸没有这些作用。随机序列寡核苷酸对培养中的任何细胞都没有任何类型的影响。然而,如果在将细胞传代到新的培养容器时添加随机序列寡核苷酸,它们会产生严重的非特异性毒性作用。这些结果表明,使用合成寡核苷酸是在含有HPV - 18 DNA的人类癌细胞行为中产生反义介导变化的有效方法。