Dass Crispin R, Choong Peter F M
Department of Orthopaedics, St. Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.
Oligonucleotides. 2010 Apr;20(2):51-60. doi: 10.1089/oli.2009.0219.
The oligonucleotide Dz13, a DNA enzyme that cleaves c-Jun mRNA, is capable of inhibiting various model tumors in mice. However, to date, a thorough examination of its target specificity in tumor cells has not been performed. In addition, an evaluation of its safety in a mammalian whole organism system has not been carried out. Dz13 mutated oligonucleotides were designed and tested in a proliferation assay. Dz13 was also tested for its safety in vivo when administered intravenously in a bolus dose, or systemically in an in utero assay. While Dz13 down-regulated target gene (c-Jun) expression in human tumor cells, c-Jun siRNA failed to cause cell growth inhibition. Furthermore, alteration of contiguous G motifs in Dz13 flanking arms inhibits cell death activity, but removal of the same from the catalytic core can increase cell death activity. A 20mer (truncated) derivative Dz13 exhibited similar activity. Dz13 was not toxic to blood and solid tissues in adult or fetal mice, though slight hepatotoxicity was noted with histology. It was also void of adverse effects to the physiological processes of angiogenesis and apoptosis. Collectively, the data support the safety of Dz13 and its activity attributed to off-target effects.
寡核苷酸Dz13是一种可切割c-Jun mRNA的DNA酶,能够抑制小鼠体内的多种模型肿瘤。然而,迄今为止,尚未对其在肿瘤细胞中的靶标特异性进行全面研究。此外,也未在哺乳动物全生物体系统中对其安全性进行评估。设计了Dz13突变寡核苷酸并在增殖试验中进行测试。还通过静脉推注给药或在子宫内试验中全身给药的方式,对Dz13在体内的安全性进行了测试。虽然Dz13在人肿瘤细胞中下调了靶基因(c-Jun)的表达,但c-Jun siRNA未能引起细胞生长抑制。此外,Dz13侧翼臂中连续G基序的改变会抑制细胞死亡活性,但从催化核心中去除相同的基序则可增加细胞死亡活性。一种20聚体(截短的)衍生物Dz13表现出类似的活性。Dz13对成年或胎儿小鼠的血液和实体组织无毒,尽管组织学检查发现有轻微肝毒性。它对血管生成和凋亡的生理过程也没有不良影响。总体而言,这些数据支持了Dz13的安全性及其归因于脱靶效应的活性。