Cancer Research UK Beatson Institute, Glasgow, United Kingdom.
University of Melbourne and Victorian Infectious Diseases Reference Laboratory, Doherty Institute of Infection and Immunity, Melbourne, Australia.
Cancer Res. 2019 Dec 1;79(23):5901-5906. doi: 10.1158/0008-5472.CAN-19-1362. Epub 2019 Aug 20.
In the March 1 issue of , we identified the Wnt receptor Fzd7 as an attractive therapeutic target for the treatment of gastric cancer. In summary, we showed that pharmacological inhibition of Wnt receptors, or genetic deletion of , blocks the initiation and growth of gastric tumors. Inhibiting Fzd receptors, specifically Fzd7, inhibits the growth of gastric cancer cells even in the presence of () mutation. Apc is located in the cytoplasm downstream of Fzd7 in the Wnt signaling cascade and mutations activate Wnt/β-catenin signaling, therefore, this result seems counterintuitive. Here, we analyze this result in greater detail in the context of current knowledge of Wnt signaling and discuss the wider implications of this aspect of Wnt signaling in other cancers.
在 3 月 1 日的那期《细胞》杂志上,我们确定了 Wnt 受体 Fzd7 是治疗胃癌的一个有吸引力的治疗靶点。总的来说,我们表明,Wnt 受体的药理抑制,或 Fzd7 的基因缺失,阻断了胃肿瘤的起始和生长。抑制 Fzd 受体,特别是 Fzd7,即使在 ()突变的情况下也能抑制胃癌细胞的生长。Apc 位于 Fzd7 在 Wnt 信号级联反应中的细胞质下游,突变激活 Wnt/β-catenin 信号,因此,这一结果似乎有违直觉。在这里,我们根据目前对 Wnt 信号的了解,更详细地分析了这一结果,并讨论了 Wnt 信号在其他癌症中的这一方面的更广泛影响。