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Obesity increased cancer risk by NKT cell depletion (PQ1)

Obesity increased cancer risk by NKT cell depletion (PQ1)
肥胖会因 NKT 细胞耗竭而增加癌症风险 (PQ1)
批准号:
8544448
负责人:
MARK A EXLEY
金额:
$17.25万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-09-15 至 2015-08-31

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中文摘要
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DESCRIPTION (provided by applicant): The obesity epidemic threatens a massive surge in metabolic disorders and other diseases including cancer. It is now known that inflammation can reinforce obesity and associated metabolic syndrome. This leads to chronic inflammation, which with other factors contribute to cancer risk. Reversing obesity or metabolic syndrome brings cancer risk toward normal levels. Natural Killer T cells (NKT) are conserved innate-like cells that can positively or negatively influence immune cells and therefore responses and outcomes in various models. We have reversed functional NKT defects in a cancer model and in vitro with human NKT. NKT are protective, but also reversibly depleted in obesity. The proposed studies will determine the mechanism for a novel role of NKT in metabolism and determine their therapeutic potential for treatment of metabolic syndrome, with implications for increased risk of cancer in obesity. Hypothesis: In obesity, we hypothesize that protective anti-tumor NKT cells are depleted throughout the body, contributing to loss of control of macrophages and consequent metabolic disease syndrome and increased cancer. This hypothesis leads to the following testable and not mutually exclusive predictions: a) Endoplasmic reticulum stress caused by obesity, leads to a loss of CD1d on the plasma membrane and therefore a decline in iNKT cells, and / or b) cancers that escape physiological control have suppressed iNKT, and this is more aggressive in obesity. Finally, there is the therapeutic question of how to reverse such defects in obesity, which we will also address. Aim 1: Determine whether cancer risk and aggressiveness are associated with iNKT loss in obesity. Aim 2: Determine whether reversing NKT cell defects can be protective in obesity-associated cancer. To perform these studies, we will exploit 2 models of cancer in which we have identified iNKT defects and combine these with obesity through high fat diets to test for increased aggressiveness. We will then determine optimal ways to reverse these defects and measure improvements in obesity, metabolic syndrome, and cancer. We are immuno-monitoring a trial of iNKT reconstitution in melanoma, so have experience in translating our findings to the clinic.
期刊论文(1)
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科研奖励(0)
会议论文
What Makes MAITs Wait?
是什么让 MAIT 等待?
DOI: 10.1016/j.immuni.2015.12.021
发表时间: 2016
期刊: Immunity
影响因子: 32.4
作者: [Exley,MarkA]
通讯作者: Exley,MarkA
Obesity increased cancer risk by NKT cell depletion (PQ1)
  • 批准号:
    8374250
  • 项目类别:
  • 资助金额:
    $22.74万
  • 财政年份:
    2012
  • 负责人:
    MARK A EXLEY
  • 依托单位:
Regulation of hepatic NKT cells by CDld+ liver cells
Regulation of hepatic NKT cells by CDld+ liver cells
Innate-like hepatic CD1d-reative NKT cells:Liver Disease
海外基金