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本文引用的文献

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Tumor Necrosis Factor-α (TNFα)-induced Ceramide Generation via Ceramide Synthases Regulates Loss of Focal Adhesion Kinase (FAK) and Programmed Cell Death.肿瘤坏死因子-α(TNFα)通过神经酰胺合酶诱导神经酰胺生成,调节粘着斑激酶(FAK)缺失和程序性细胞死亡。
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Enhanced colonic tumorigenesis in alkaline sphingomyelinase (NPP7) knockout mice.碱性鞘磷脂酶(NPP7)基因敲除小鼠的结肠肿瘤发生增强。
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Sphingosine-1-phosphate lyase downregulation promotes colon carcinogenesis through STAT3-activated microRNAs.鞘氨醇-1-磷酸裂解酶下调通过STAT3激活的微小RNA促进结肠癌发生。
J Clin Invest. 2014 Dec;124(12):5368-84. doi: 10.1172/JCI74188. Epub 2014 Oct 27.
4
Sphingosine kinase 1 promotes malignant progression in colon cancer and independently predicts survival of patients with colon cancer by competing risk approach in South asian population.鞘氨醇激酶 1 通过竞争风险方法促进亚洲南部人群结肠癌的恶性进展,并独立预测结肠癌患者的生存。
Clin Transl Gastroenterol. 2014 Feb 27;5(2):e51. doi: 10.1038/ctg.2013.21.
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Aberrant crypt foci: the case for inclusion as a biomarker for colon cancer.异常隐窝病灶:作为结直肠癌生物标志物的入选理由。
Cancers (Basel). 2010 Sep 16;2(3):1705-16. doi: 10.3390/cancers2031705.
6
New insight into the structure, reaction mechanism, and biological functions of neutral ceramidase.对中性神经酰胺酶的结构、反应机制及生物学功能的新见解。
Biochim Biophys Acta. 2014 May;1841(5):682-91. doi: 10.1016/j.bbalip.2013.09.008. Epub 2013 Sep 21.
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Sphingolipids in colon cancer.结肠癌中的鞘脂类
Biochim Biophys Acta. 2014 May;1841(5):773-82. doi: 10.1016/j.bbalip.2013.09.007. Epub 2013 Sep 21.
8
Sphingosine-1-phosphate links persistent STAT3 activation, chronic intestinal inflammation, and development of colitis-associated cancer.鞘氨醇-1-磷酸将持续的 STAT3 激活、慢性肠道炎症和结肠炎相关癌症的发展联系起来。
Cancer Cell. 2013 Jan 14;23(1):107-20. doi: 10.1016/j.ccr.2012.11.013. Epub 2012 Dec 27.
9
Ceramide-orchestrated signalling in cancer cells.细胞癌变过程中的神经酰胺信号传导
Nat Rev Cancer. 2013 Jan;13(1):51-65. doi: 10.1038/nrc3398. Epub 2012 Dec 13.
10
Sphingosine 1-phosphate induces filopodia formation through S1PR2 activation of ERM proteins.鞘氨醇 1-磷酸通过 S1PR2 激活 ERM 蛋白诱导丝状伪足形成。
Biochem J. 2013 Feb 1;449(3):661-72. doi: 10.1042/BJ20120213.

中性神经酰胺酶在结肠癌中的作用。

Role of neutral ceramidase in colon cancer.

作者信息

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

机构信息

Department of Medicine, Stony Brook University, New York, USA.

Stony Brook Cancer Center, Stony Brook University, Stony Brook, New York, USA.

出版信息

FASEB J. 2016 Dec;30(12):4159-4171. doi: 10.1096/fj.201600611R. Epub 2016 Sep 8.

DOI:10.1096/fj.201600611R
PMID:27609772
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5102116/
Abstract

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.

摘要

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