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Sphingosine-1-phosphate: Driver of NFB and STAT3 persistent activation in chronic intestinal inflammation and colitis-associated cancer.

机译:Sphingosine-1-phosphate:负反馈和STAT3的司机持续激活慢性肠道炎症和colitis-associated癌症。

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摘要

Inflammatory bowel disease is associated with an increased risk of colorectal cancer. Colitis-associated cancer is a classical inflammation-driven cancer in which constitutive NFB and STAT3 activation drive tumorigenesis. Recent findings published by Liang et al. in Cancer Cell demonstrate that sphingosine kinase 1 (SphK1)-mediated upregulation of sphingosine-1-phosphate (S1P) drives a persistent NFB/IL-6/STAT3/sphingosine-1-phosphate receptor 1 (S1PR1) amplification loop that is critical to the development of chronic colitis and colitis-associated cancer. FTY720, an antagonist of S1PR1, abolished persistent NFB/IL-6/STAT3 signaling and reduced the development and progression of colitis-associated cancer. Targeting SphK1/S1P/S1PR1 may provide a therapeutic option to prevent the progression of colitis to cancer.ISSN Print 2162-3988
机译:炎症性肠病与一个关联增加结直肠癌的风险。Colitis-associated癌症是一种经典本构inflammation-driven癌症负反馈和STAT3激活驱动肿瘤发生。最近发现梁等人发表癌症细胞表明鞘氨醇激酶1(SphK1)介导upregulationsphingosine-1-phosphate (S1P)驱动一个持久负反馈/ il - 6 / STAT3 / sphingosine-1-phosphate受体1(S1PR1)扩增循环至关重要慢性结肠炎和的发展colitis-associated癌症。S1PR1,废除持续负反馈/ il - 6 / STAT3信号,降低了开发和colitis-associated癌症的发展。针对SphK1 / S1P S1PR1可能提供一个治疗选择预防的发展结肠炎癌症。

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