Suppr超能文献

用于治疗HPV16阳性宫颈癌的新型高效特异性E6和E7小干扰RNA

New highly potent and specific E6 and E7 siRNAs for treatment of HPV16 positive cervical cancer.

作者信息

Yamato K, Yamada T, Kizaki M, Ui-Tei K, Natori Y, Fujino M, Nishihara T, Ikeda Y, Nasu Y, Saigo K, Yoshinouchi M

机构信息

Molecular Cellular Oncology and Microbiology, Graduate School, Tokyo Medical and Dental University, Tokyo, Japan.

出版信息

Cancer Gene Ther. 2008 Mar;15(3):140-53. doi: 10.1038/sj.cgt.7701118. Epub 2007 Dec 21.

Abstract

Persistent infection by high-risk types of human papillomaviruses (HPV) is a necessary cause of cervical cancer, with HPV16 the most prevalent, accounting for more than 50% of reported cases. The virus encodes the E6 and E7 oncoproteins, whose expression is essential for maintenance of the malignant phenotype. To select efficacious siRNAs applicable to RNAi therapy for patients with HPV16+ cervical cancer, E6 and E7 siRNAs were designed using siDirect computer software, after which 10 compatible with all HPV16 variants were selected, and then extensively examined for RNAi activity and specificity using HPV16+ and HPV16-cells. Three siRNAs with the highest RNAi activities toward E6 and E7 expression, as well as specific and potent growth suppression of HPV16+ cancer cells as low as 1 nM were chosen. Growth suppression was accompanied by accumulation of p53 and p21(WAF1/CIP1), as well as morphological and cytochemical changes characteristic of cellular senescence. Antitumor activity of one of the selected siRNAs was confirmed by retarded tumor growth of HPV16+ cells in NOD/SCID mice when locally injected in a complex with atelocollagen. Our results demonstrate that these E6 and E7 siRNAs are promising therapeutic agents for treatment of virus-related cancer.

摘要

高危型人乳头瘤病毒(HPV)的持续感染是宫颈癌的必要病因,其中HPV16最为常见,占报告病例的50%以上。该病毒编码E6和E7癌蛋白,它们的表达对于维持恶性表型至关重要。为了筛选适用于HPV16阳性宫颈癌患者RNA干扰治疗的有效小干扰RNA(siRNA),利用siDirect计算机软件设计了E6和E7的siRNA,之后筛选出10种与所有HPV16变体兼容的siRNA,然后使用HPV16阳性和HPV16阴性细胞对其RNA干扰活性和特异性进行了广泛检测。选择了三种对E6和E7表达具有最高RNA干扰活性、对低至1 nM的HPV16阳性癌细胞具有特异性且强效生长抑制作用的siRNA。生长抑制伴随着p53和p21(WAF1/CIP1)的积累,以及细胞衰老特征性的形态学和细胞化学变化。当与去端肽胶原复合局部注射时,NOD/SCID小鼠体内HPV16阳性细胞的肿瘤生长延迟,证实了所选siRNA之一的抗肿瘤活性。我们的结果表明,这些E6和E7的siRNA有望成为治疗病毒相关癌症的治疗药物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验