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高胆固醇血症通过减少造血干细胞产生自然杀伤T细胞和γδT细胞来增加结直肠癌发病率。

Hypercholesterolemia Increases Colorectal Cancer Incidence by Reducing Production of NKT and γδ T Cells from Hematopoietic Stem Cells.

作者信息

Tie Guodong, Yan Jinglian, Khair Lyne, Messina Julia A, Deng April, Kang Joonsoo, Fazzio Thomas, Messina Louis M

机构信息

Diabetes Center of Excellence and Division of Vascular and Endovascular Surgery, University of Massachusetts Medical School, Worcester, Massachusetts.

Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina.

出版信息

Cancer Res. 2017 May 1;77(9):2351-2362. doi: 10.1158/0008-5472.CAN-16-1916. Epub 2017 Mar 1.

DOI:10.1158/0008-5472.CAN-16-1916
PMID:28249902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6193767/
Abstract

Obesity will soon surpass smoking as the most preventable cause of cancer. Hypercholesterolemia, a common comorbidity of obesity, has been shown to increase cancer risk, especially colorectal cancer. However, the mechanism by which hypercholesterolemia or any metabolic disorder increases cancer risk remains unknown. In this study, we show that hypercholesterolemia increases the incidence and pathologic severity of colorectal neoplasia in two independent mouse models. Hypocholesterolemia induced an oxidant stress-dependent increase in miR101c, which downregulated Tet1 in hematopoietic stem cells (HSC), resulting in reduced expression of genes critical to natural killer T cell (NKT) and γδ T-cell differentiation. These effects reduced the number and function of terminally differentiated NKT and γδ T cells in the thymus, the colon submucosa, and during early tumorigenesis. These results suggest a novel mechanism by which a metabolic disorder induces epigenetic changes to reduce lineage priming of HSC toward immune cells, thereby compromising immunosurveillance against cancer. .

摘要

肥胖症很快将超越吸烟,成为最可预防的癌症病因。高胆固醇血症是肥胖症常见的合并症,已被证明会增加癌症风险,尤其是结直肠癌风险。然而,高胆固醇血症或任何代谢紊乱增加癌症风险的机制仍不清楚。在本研究中,我们表明,在两个独立的小鼠模型中,高胆固醇血症会增加结直肠肿瘤形成的发生率和病理严重程度。低胆固醇血症诱导了miR101c的氧化应激依赖性增加,这下调了造血干细胞(HSC)中的Tet1,导致对自然杀伤T细胞(NKT)和γδT细胞分化至关重要的基因表达减少。这些效应减少了胸腺、结肠黏膜下层以及早期肿瘤发生过程中终末分化的NKT和γδT细胞的数量和功能。这些结果提示了一种新机制,即代谢紊乱通过诱导表观遗传变化来减少造血干细胞向免疫细胞的谱系启动,从而损害对癌症的免疫监视。

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Sci Rep. 2016 May 26;6:26591. doi: 10.1038/srep26591.
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Shared Risk Factors in Cardiovascular Disease and Cancer.心血管疾病和癌症的共同风险因素。
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Obesity and Cancer: The Oil that Feeds the Flame.肥胖与癌症:火上浇油。
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Region-Specific CD16 Neutrophils Promote Colorectal Cancer Progression by Inhibiting Natural Killer Cells.区域特异性 CD16 中性粒细胞通过抑制自然杀伤细胞促进结直肠癌进展。
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Hypercholesterolemia impairs collateral artery enlargement by ten-eleven translocation 1-dependent hematopoietic stem cell autonomous mechanism in a murine model of limb ischemia.在肢体缺血小鼠模型中,高胆固醇血症通过10-11易位蛋白1依赖性造血干细胞自主机制损害侧支动脉扩张。
JVS Vasc Sci. 2024 Apr 6;5:100203. doi: 10.1016/j.jvssci.2024.100203. eCollection 2024.
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Hypoxia-induced NOS1 as a therapeutic target in hypercholesterolemia-related colorectal cancer.缺氧诱导的一氧化氮合酶1作为高胆固醇血症相关结直肠癌的治疗靶点。
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Statins as anti-tumor agents: A paradigm for repurposed drugs.他汀类药物作为抗肿瘤药物:重新定位药物的范例。
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