Cancer Research Institute, Seoul National University College of Medicine, Seoul, South Korea.
Invest New Drugs. 2012 Dec;30(6):2148-60. doi: 10.1007/s10637-011-9782-6. Epub 2011 Dec 25.
Biliary tract cancer (BTC) is associated with poor survival and unresponsiveness to chemotherapy. Targeted therapies for BTC have been studied, and HER family members are promising therapeutic targets in BTC. In this study, we evaluated the efficacy of PF00299804, an irreversible pan-HER inhibitor, in eight BTC cell lines alone or combined with gemcitabine. PF00299804 potently inhibited the growth of two cell lines (SNU308 and SNU478) out of the eight BTC cell lines as a single agent. PF00299804 blocked HER family and downstream signaling pathways, inducing G1 arrest or apoptosis. Moreover, PF00299804 exerted synergistic effects with gemcitabine in seven of the eight BTC cell lines, possibly through the regulation of the genes involved in the response to gemcitabine, such as TS (thymidylate synthase), RRM1 (ribonucleotide reductase), and MAGEH1, which is negatively correlated with gemcitabine sensitivity. Our results support the need for further study of PF00299804 alone or combined with gemcitabine for the treatment of BTC.
胆管癌(BTC)与生存不良和对化疗无反应有关。已经研究了针对 BTC 的靶向治疗方法,HER 家族成员是 BTC 中有前途的治疗靶点。在这项研究中,我们评估了不可逆的泛 HER 抑制剂 PF00299804 单独或联合吉西他滨在八种 BTC 细胞系中的疗效。PF00299804 作为单一药物强烈抑制了八种 BTC 细胞系中的两种细胞系(SNU308 和 SNU478)的生长。PF00299804 阻断了 HER 家族和下游信号通路,诱导 G1 期停滞或细胞凋亡。此外,PF00299804 在八种 BTC 细胞系中的七种细胞系中与吉西他滨具有协同作用,可能通过调节与吉西他滨反应相关的基因,如胸苷酸合成酶(TS)、核糖核苷酸还原酶(RRM1)和 MAGEH1 的表达,MAGEH1 与吉西他滨的敏感性呈负相关。我们的研究结果支持需要进一步研究 PF00299804 单独或联合吉西他滨治疗 BTC。