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血管生成素样蛋白4通过过氧化物酶体增殖物激活受体信号通路在代谢与癌症相互作用中的潜在作用

Potential Role of ANGPTL4 in the Cross Talk between Metabolism and Cancer through PPAR Signaling Pathway.

作者信息

La Paglia Laura, Listì Angela, Caruso Stefano, Amodeo Valeria, Passiglia Francesco, Bazan Viviana, Fanale Daniele

机构信息

ICAR-CNR, National Research Council of Italy, 90146 Palermo, Italy.

Department of Surgical, Oncological and Oral Sciences, Section of Medical Oncology, University of Palermo, 90127 Palermo, Italy.

出版信息

PPAR Res. 2017;2017:8187235. doi: 10.1155/2017/8187235. Epub 2017 Jan 15.

Abstract

The angiopoietin-like 4 (ANGPTL4) protein belongs to a superfamily of secreted proteins structurally related to factors modulating angiogenesis known as angiopoietins. At first, ANGPTL4 has been identified as an adipokine exclusively involved in lipid metabolism, because of its prevalent expression in liver and adipose tissue. This protein regulates lipid metabolism by inhibiting lipoprotein lipase (LPL) activity and stimulating lipolysis of white adipose tissue (WAT), resulting in increased levels of plasma triglycerides (TG) and fatty acids. Subsequently, ANGPTL4 has been shown to be involved in several nonmetabolic and metabolic conditions, both physiological and pathological, including angiogenesis and vascular permeability, cell differentiation, tumorigenesis, glucose homoeostasis, lipid metabolism, energy homeostasis, wound healing, inflammation, and redox regulation. The transcriptional regulation of ANGPTL4 can be modulated by several transcription factors, including PPAR, PPAR/, PPAR, and HIF-1, and nutritional and hormonal conditions. Several studies showed that high levels of ANGPTL4 are associated with poor prognosis in patients with various solid tumors, suggesting an important role in cancer onset and progression, metastasis, and anoikis resistance. Here, we have discussed the potential role of ANGPTL4 in mediating the cross talk between metabolic syndromes, such as diabetes and obesity, and cancer through regulation of its expression by PPARs.

摘要

血管生成素样4(ANGPTL4)蛋白属于一个分泌蛋白超家族,其结构与调节血管生成的因子(称为血管生成素)相关。起初,ANGPTL4被鉴定为一种仅参与脂质代谢的脂肪因子,因为它在肝脏和脂肪组织中普遍表达。该蛋白通过抑制脂蛋白脂肪酶(LPL)活性和刺激白色脂肪组织(WAT)的脂解作用来调节脂质代谢,从而导致血浆甘油三酯(TG)和脂肪酸水平升高。随后,ANGPTL4已被证明参与多种非代谢和代谢状况,包括生理和病理状况,如血管生成和血管通透性、细胞分化、肿瘤发生、葡萄糖稳态、脂质代谢、能量稳态、伤口愈合、炎症和氧化还原调节。ANGPTL4的转录调控可由多种转录因子调节,包括PPAR、PPAR/、PPAR和HIF-1,以及营养和激素状况。多项研究表明,高水平的ANGPTL4与各种实体瘤患者的不良预后相关,提示其在癌症发生、进展、转移和失巢凋亡抵抗中起重要作用。在此,我们讨论了ANGPTL4通过PPARs调节其表达在介导代谢综合征(如糖尿病和肥胖)与癌症之间的相互作用中的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e983/5274667/3ade4d3bbceb/PPAR2017-8187235.001.jpg

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