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Identification of quinazoline compounds as novel potent inhibitors of Wnt/β-catenin signaling in colorectal cancer cells

机译:喹唑啉化合物在大肠癌细胞中作为Wnt /β-catenin信号的新型有效抑制剂的鉴定

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摘要

The Wnt/β-catenin signaling pathway is critical for the initiation and progression of most colon cancers, and has emerged as one of the most promising targets for colorectal cancer chemoprevention and treatment. In this study, we have discovered a structurally related series of quinazolines as potent inhibitors of Wnt/β-catenin signaling in colorectal cancer cells harboring mutations in CTNNB1 or APC. We showed that the quinazoline leads suppressed Wnt/β-catenin signaling without altering the level of β-catenin protein in colorectal cancer cells, suggesting that they act on the downstream elements of the pathway. Moreover, the quinazoline leads displayed potent anticancer activities with IC50 values between 4.9 and 17.4 μM in colorectal cancer cells. Importantly, we also found that a structurally related quinazoline lacking inhibitory effect on Wnt/β-catenin signaling was unable to suppress colorectal cancer cell proliferation. Together, these results suggest that the quinazoline lead compounds identified in this study have therapeutic potential for the prevention and treatment of colorectal cancer.
机译:Wnt /β-catenin信号传导途径对大多数结肠癌的发生和发展至关重要,并且已成为大肠癌化学预防和治疗的最有希望的靶标之一。在这项研究中,我们发现了一系列与结构相关的喹唑啉类化合物,它们是Wnt /β-catenin信号传导的有效抑制剂,可抑制CTNNB1或APC突变的结直肠癌细胞。我们显示喹唑啉导致抑制的Wnt /β-catenin信号传导,而不会改变大肠癌细胞中β-catenin蛋白的水平,表明它们作用于该途径的下游元素。此外,喹唑啉铅在结直肠癌细胞中显示出有效的抗癌活性,IC50值在4.9和17.4μM之间。重要的是,我们还发现对Wnt /β-catenin信号缺乏抑制作用的结构相关的喹唑啉不能抑制结直肠癌细胞的增殖。总之,这些结果表明,在这项研究中确定的喹唑啉铅化合物具有预防和治疗结肠直肠癌的治疗潜力。

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