Ohashi Wakana, Yamamine Naoki, Imura Johji, Hattori Yuichi
Department of Molecular and Medical Pharmacology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama 930-0194, Japan.
Department of Molecular and Medical Pharmacology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama 930-0194, Japan.
Biochem Biophys Res Commun. 2017 Nov 25;493(3):1342-1348. doi: 10.1016/j.bbrc.2017.09.161. Epub 2017 Sep 29.
Aberrant activation of Wnt signaling plays a pivotal role in the development of human cancers including colon cancer. Small compounds that regulate Wnt signaling are attractive candidate for the colon cancer therapy. Here, we showed that SKL2001, which has been identified as an activator for Wnt signaling by disrupting the Axin/β-Catenin complex, negatively regulates growth of colon cancer spheroids cultured in the 3D condition that simulates tumor microenvironment in vivo. SKL2001 inhibited proliferation of colon cancer cells cultured in 3D spheroid and induced them accumulation in the G0/G1 phase of the cell cycle with a reduced c-myc level. To examine the potential of arrested cells to recover, colon cancer spheroids that were treated with SKL2001 were then cultured in the SKL2001-free medium. We found that SKL2001-treated cells were resumed cell cycle progression and proliferated in the SKL2001-free medium. Notably, SKL2001 facilitated round-shape spheroid formation. This was associated with upregulated expressions of E-cadherin and β-Catenin. These findings suggest that SKL2001 can suppress colon cancer spheroid growth through regulating cell cycle progression and cadherin/catenin mediated cell-cell contact.
Wnt信号通路的异常激活在包括结肠癌在内的人类癌症发展中起关键作用。调节Wnt信号通路的小分子化合物是结肠癌治疗的有吸引力的候选物。在此,我们表明,SKL2001已被确定为通过破坏Axin/β-连环蛋白复合物来激活Wnt信号通路,它对在模拟体内肿瘤微环境的三维条件下培养的结肠癌细胞球的生长具有负向调节作用。SKL2001抑制在三维细胞球中培养的结肠癌细胞的增殖,并诱导它们在细胞周期的G0/G1期积累,同时c-myc水平降低。为了检测停滞细胞恢复的潜力,用SKL2001处理过的结肠癌细胞球随后在不含SKL2001的培养基中培养。我们发现,用SKL2001处理过的细胞在不含SKL2001的培养基中恢复了细胞周期进程并开始增殖。值得注意的是,SKL2001促进了圆形细胞球的形成。这与E-钙黏蛋白和β-连环蛋白表达上调有关。这些发现表明,SKL2001可以通过调节细胞周期进程以及钙黏蛋白/连环蛋白介导的细胞间接触来抑制结肠癌细胞球的生长。