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

Authors :
Laura La Paglia
Angela Listì
Stefano Caruso
Valeria Amodeo
Francesco Passiglia
Viviana Bazan
Daniele Fanale
Source :
PPAR Research, Vol 2017 (2017)
Publication Year :
2017
Publisher :
Hindawi Limited, 2017.

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 PPARα, PPARβ/δ, PPARγ, and HIF-1α, 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.

Subjects

Subjects :
Biology (General)
QH301-705.5

Details

Language :
English
ISSN :
16874757 and 16874765
Volume :
2017
Database :
Directory of Open Access Journals
Journal :
PPAR Research
Publication Type :
Academic Journal
Accession number :
edsdoj.bf5d54e5d37646e7b9e938b32d0c032c
Document Type :
article
Full Text :
https://doi.org/10.1155/2017/8187235