Department of Pathological Anatomy, Nantong University, Nantong, Jiangsu 226001, P.R. China.
Mol Med Rep. 2013 Oct;8(4):1037-42. doi: 10.3892/mmr.2013.1646. Epub 2013 Aug 19.
Hepatocellular carcinoma (HCC) is one of the most common types of malignant tumor. Studies have demonstrated that the toll‑like receptor 3 (TLR3)/interferon pathway is inhibitory in cancer cell proliferation, suggesting that the activation of this pathway may have therapeutic potential. In the present study, the inhibitory effects of BM‑06, a double‑stranded (ds)RNA TLR3 agonist, against HCC were studied in vivo. Using a 2‑acetylaminofluorene-induced HCC rat model, histological examination and analysis of corresponding biomarkers following treatment with BM-06, showed a decrease in tumor growth and cell proliferation, and an increase in apoptosis compared with that in a phosphate‑buffered saline control group. In addition, the observed antitumor effect of BM‑06 in the HCC rat model was demonstrated to be superior to the known TLR3 agonist, polyinosinic-polycytidylic acid.
肝细胞癌 (HCC) 是最常见的恶性肿瘤类型之一。研究表明,Toll 样受体 3 (TLR3)/干扰素通路在癌细胞增殖中具有抑制作用,提示该通路的激活可能具有治疗潜力。在本研究中,研究了双链 (ds)RNA TLR3 激动剂 BM-06 对 HCC 的体内抑制作用。使用 2-乙酰氨基芴诱导的 HCC 大鼠模型,用 BM-06 处理后进行组织学检查和相应生物标志物的分析,与磷酸盐缓冲盐水对照组相比,肿瘤生长和细胞增殖减少,凋亡增加。此外,BM-06 在 HCC 大鼠模型中的抗肿瘤作用优于已知的 TLR3 激动剂聚肌胞苷酸。