Futami Kazunobu, Kumagai Emi, Makino Hiroshi, Sato Ayumi, Takagi Motoki, Shimamoto Akira, Furuichi Yasuhiro
GeneCare Research Institute, 19-2 Kajiwara, Kamakura, Kanagawa 247-0063, Japan.
Cancer Sci. 2008 Jun;99(6):1227-36. doi: 10.1111/j.1349-7006.2008.00794.x. Epub 2008 Apr 14.
Small interfering RNAs (siRNAs) are expected to have a medical application in human therapy as drugs with a high specificity for their molecular target mRNAs. RecQL1 DNA helicase in the human RecQ helicase family participates in DNA repair and recombination pathways in the cell cycle of replication. Silencing the RecQL1 expression by RecQL1-siRNA induces mitotic death in vitro specifically in growing cancer cells. By contrast, the same RecQL1 silencing does not affect the growth of normal cells, emphasizing that RecQL1 helicase is an ideal molecular target for cancer therapy. In this study, we show that local and systemic administration of RecQL1-siRNA mixed with polyethyleneimine polymer or cationic liposomes prevented cancer cell proliferation in vivo in mouse models of cancer without noticeable adverse effects. The results indicate that RecQL1-siRNA in a complex with a cationic polymer is a very promising anticancer drug candidate, and that in particular, RecQL1-siRNA formulated with a cationic liposome has an enormous potential to be used by intravenous injection for therapy specific for liver cancers, including metastasized cancers from the colon and pancreas.
小干扰RNA(siRNAs)有望作为对其分子靶标mRNA具有高特异性的药物在人类治疗中得到医学应用。人类RecQ解旋酶家族中的RecQL1 DNA解旋酶参与复制细胞周期中的DNA修复和重组途径。通过RecQL1-siRNA沉默RecQL1表达可在体外特异性地诱导正在生长的癌细胞发生有丝分裂死亡。相比之下,相同的RecQL1沉默并不影响正常细胞的生长,这突出表明RecQL1解旋酶是癌症治疗的理想分子靶标。在本研究中,我们表明,将RecQL1-siRNA与聚乙烯亚胺聚合物或阳离子脂质体混合进行局部和全身给药,可在小鼠癌症模型中体内阻止癌细胞增殖,且无明显不良反应。结果表明,与阳离子聚合物复合的RecQL1-siRNA是一种非常有前景的抗癌药物候选物,特别是,用阳离子脂质体制备的RecQL1-siRNA具有通过静脉注射用于治疗包括结肠癌和胰腺癌转移癌在内的肝癌的巨大潜力