Experimental Therapy Unit, Laboratory of Oncology, G. Gaslini Children's Hospital, Genoa, Italy.
Cancer Res. 2010 Dec 1;70(23):9816-26. doi: 10.1158/0008-5472.CAN-10-1251. Epub 2010 Oct 8.
The Toll-like receptor 9 (TLR9) evolved to cope with pathogens, but it is expressed in a variety of tumors for reasons that are unclear. In this study, we report that neuroblastoma (NB) cells express functional TLR9. Liposome-complexed CpG oligonucleotides inhibited the proliferation of TLR9-expressing NB cells and induced caspase-dependent apoptotic cell death. Inhibitory oligonucleotides (iODNs) abrogated these effects. RNA interference reduced TLR9 expression but not to the level where functional responses to CpG were abolished. Compared with free CpG, liposomal formulations of NB-targeted CpG (TL-CpG) significantly prolonged the survival of mice bearing NB tumor xenografts. While CpG alone lacked antitumor efficacy in NOD/SCID/IL2rg(-/-) mice, TL-CpG retained significant efficacy related to direct effects on tumor cells. TLR9 expression in primary human NB specimens was found to correlate inversely with disease stage. Our findings establish functional expression of TLR9 in NB and suggest that TLR9 may represent a novel theranostic target in this disease.
Toll 样受体 9(TLR9)的进化是为了应对病原体,但它在许多肿瘤中表达,其原因尚不清楚。在这项研究中,我们报告神经母细胞瘤(NB)细胞表达功能性 TLR9。脂质体复合 CpG 寡核苷酸抑制 TLR9 表达的 NB 细胞增殖,并诱导 caspase 依赖性凋亡细胞死亡。抑制性寡核苷酸(iODN)消除了这些作用。RNA 干扰降低了 TLR9 的表达,但并未达到功能性 CpG 反应被消除的水平。与游离 CpG 相比,针对 NB 的靶向 CpG(TL-CpG)的脂质体制剂显著延长了携带 NB 肿瘤异种移植物的小鼠的存活时间。虽然 CpG 单独在 NOD/SCID/IL2rg(-/-) 小鼠中缺乏抗肿瘤功效,但 TL-CpG 保留了与直接作用于肿瘤细胞相关的显著功效。在原发性人 NB 标本中发现 TLR9 的表达与疾病分期呈负相关。我们的研究结果确立了 TLR9 在 NB 中的功能性表达,并表明 TLR9 可能成为该疾病的一种新的治疗靶点。