Regulation of Lipid Droplets and FOXO3 in Intestinal Epithelial Cell Proliferatio

描述（由申请人提供）：肥胖和超重，在过去二十年在发达国家已经成为巨大的流行病，与一系列广泛的疾病有关，包括不同器官的癌症，如结肠癌。迄今为止，这些关联的潜在机制尚未完全了解。一种新出现的可能性是，肥胖个体组织中积累的过量脂质直接刺激了结肠肿瘤的发展。细胞内脂质储存在脂滴（ld）中，脂滴是脂肪组织中的动态细胞器，也存在于许多人类肿瘤中。据信，ld是驱动增殖的能量来源，是肿瘤进展的标志；然而，它们的调节和功能尚不清楚。我们的初步数据显示，肥胖小鼠的结肠以及炎症和肿瘤结肠组织中的LD积累增加。此外，LDs受到肿瘤抑制因子FOXO3的负调控，而刺激LDs的积累导致FOXO3活性的丧失。因此，我们提出存在一个LD-FOXO3网络，该网络还包括PI3K和SIRT6（甘油三酯（tg）的负调节因子）。此外，初步数据表明LD-FOXO3网络在结肠癌细胞增殖中起关键作用，也在肥胖影响结肠上皮中起作用。

DESCRIPTION (provided by applicant): Obesity and overweight, which have been immense epidemics in developed countries for the last two decades, are associated with a wide array of diseases including cancer of different organs such as the colon. To date, the underlying mechanisms for these associations are not completely understood. One of emerging possibilities is that excess lipids accumulated in the tissue of obese individuals directly stimulates progression of colonic tumors. Intracellular lipids are stored in lipid droplets (LDs), dynamic organelles found in adipose tissue, as well as in many human tumors. It is believed that LDs are the source of energy that drives proliferation, a hallmark of tumor progression; however, their regulation and function are not well understood. Our preliminary data reveals that LD accumulation is increased in the colon of obese mice as well as in inflamed and neoplastic colonic tissue. Moreover, LDs are negatively regulated by tumor suppressor FOXO3, while stimulating LDs accumulation leads to a loss of FOXO3 activity. Thus we propose the existence of an LD-FOXO3 network that also includes PI3K and SIRT6 (a negative regulator of triglycerides (TGs). Moreover, preliminary data suggested that the LD-FOXO3 network is critical in proliferation of colonic cancer cells and also operates in obesity influence colonic epithelium. There is support that the LD-FOXO3 network is upstream control by EGFR and/or PGE2, while downstream modifies cell cycle regulators and triglyceride synthesis. The central hypothesis of this proposal is that proliferation in colonic cells controlled by LD-FOXO3 network leads to coordinate LD accumulation and cell cycle progression dependent on loss of FOXO3 is one mechanism responsible for obesity related colon tumor progression. The following Specific Aims are proposed: Aim 1. To assess if the LD induced proliferative response in colonic cancer cells depends on FOXO3 activity via (a) activation of EGFR and whether this is dependent on PGE2, (b) PI3K dependent loss of FOXO3 cell cycle arrest, and (c) SIRT6 dependent, a negative regulator of TGs in colon cancer cells. Aim 2. To determine if TNF-induced proliferation and consequent LD accumulation are due to activation of EGFR, PGE2 and a loss of FOXO3 cell cycle arrest and SIRT6 (in vitro), and (b) to find if selective blockade of LD in TNF treated Foxo3 or EGFR deficient mice suppresses proliferation of colonic epithelia by promoting Foxo3 dependent SIRT6 and cell cycle arrest and TGs. Aim 3. To assess if obesity and a deficiency in Foxo3 (a) exacerbated adenoma progression in DSS/AOM model leading to alterations in regulators of G0-G1 checkpoint and TGs, (b) if adenoma progression is suppressed by selective blockade of LD, PGE2, or TNF, and (c) to identify the Foxo3 dependent genes regulating lipid metabolism. Findings from the proposed study would have significant positive effects on human health by presenting the LD-FOXO3 network as a novel therapeutic target. Although mechanisms of colon cancer progression are complex, the inhibition of LDs may provide an effective blockade to tumor progression in patients with obesity promoted colonic tumor progression. PUBLIC HEALTH RELEVANCE: Obesity and general overweight, which have been immense epidemics in developed countries for the last two decades, are associated with increased risk of a spectrum of tumors including colon cancer. Once cancer develops, overweight or obese individuals are at larger risk of recurrence and decreased chance of survival. The mechanisms underlying why obesity causes increased risk of tumors are unclear. One possibility which is not explored, is that excess lipids accumulated in non-fat tissue of obese individual, promote tumor development. In support of this theory is that accumulation of lipids in cancer cells is critical i tumor growth. Our preliminary data suggests lipid accumulation and activity of FOXO3 tumor suppressor depend on each other and activation of their network may drive colon cancer progression. The goal of this proposed study is to define the mechanisms responsible for colonic cancer progression induced by lipid accumulation and suppressed by FOXO3 activity and to study the involvement of this mechanism in obesity promoted colonic tumor progression. Significance: This knowledge will allow us to establish the therapeutic potential of lipids in the treatment of colonic tumors. This data is expected to have significant positive effects on human health, because they will lead to an understanding of the mechanisms by which lipids stimulate progression of colonic tumors and will provide the foundation necessary for further development of new pharmacological options for treatment.