García-Barros Mónica, Coant Nicolas, Kawamori Toshihiko, Wada Masayuki, Snider Ashley J, Truman Jean-Philip, Wu Bill X, Furuya Hideki, Clarke Christopher J, Bialkowska Agnieszka B, Ghaleb Amr, Yang Vincent W, Obeid Lina M, Hannun Yusuf A
Department of Medicine, Stony Brook University, New York, USA.
Stony Brook Cancer Center, Stony Brook University, Stony Brook, New York, USA.
FASEB J. 2016 Dec;30(12):4159-4171. doi: 10.1096/fj.201600611R. Epub 2016 Sep 8.
Alterations in sphingolipid metabolism, especially ceramide and sphingosine 1-phosphate, have been linked to colon cancer, suggesting that enzymes of sphingolipid metabolism may emerge as novel regulators and targets in colon cancer. Neutral ceramidase (nCDase), a key enzyme in sphingolipid metabolism that hydrolyzes ceramide into sphingosine, is highly expressed in the intestine; however, its role in colon cancer has not been defined. Here we show that molecular and pharmacological inhibition of nCDase in colon cancer cells increases ceramide, and this is accompanied by decreased cell survival and increased apoptosis and autophagy, with minimal effects on noncancerous cells. Inhibition of nCDase resulted in loss of β-catenin and inhibition of ERK, components of pathways relevant for colon cancer development. Furthermore, inhibition of nCDase in a xenograft model delayed tumor growth and increased ceramide while decreasing proliferation. It is noteworthy that mice lacking nCDase treated with azoxymethane were protected from tumor formation. Taken together, these studies show that nCDase is pivotal for regulating initiation and development of colon cancer, and these data suggest that this enzyme is a suitable and novel target for colon cancer therapy.-García-Barros, M., Coant, N., Kawamori, T., Wada, M., Snider, A. J., Truman, J.-P., Wu, B. X., Furuya, H., Clarke, C. J., Bialkowska, A. B., Ghaleb, A., Yang, V. W., Obeid, L. M., Hannun, Y. A. Role of neutral ceramidase in colon cancer.
鞘脂代谢的改变,尤其是神经酰胺和1-磷酸鞘氨醇的改变,与结肠癌有关,这表明鞘脂代谢酶可能成为结肠癌新的调节因子和靶点。中性神经酰胺酶(nCDase)是鞘脂代谢中的一种关键酶,可将神经酰胺水解为鞘氨醇,在肠道中高度表达;然而,其在结肠癌中的作用尚未明确。在此我们表明,对结肠癌细胞中nCDase的分子抑制和药理抑制会增加神经酰胺,同时伴随着细胞存活率降低、凋亡和自噬增加,而对非癌细胞的影响最小。抑制nCDase导致β-连环蛋白缺失和ERK抑制,ERK是与结肠癌发展相关途径的组成部分。此外,在异种移植模型中抑制nCDase可延缓肿瘤生长、增加神经酰胺并减少增殖。值得注意的是,用氧化偶氮甲烷处理的缺乏nCDase的小鼠可免受肿瘤形成。综上所述,这些研究表明nCDase对调节结肠癌的起始和发展至关重要,这些数据表明该酶是结肠癌治疗的一个合适且新的靶点。-加西亚-巴罗斯,M.,科安特,N.,川森,T.,和田,M.,斯奈德,A.J.,杜鲁门,J.-P.,吴,B.X.,古屋,H.,克拉克,C.J.,比亚尔科夫斯卡,A.B.,加勒布,A.,杨,V.W.,奥贝德,L.M.,汉农,Y.A. 中性神经酰胺酶在结肠癌中的作用