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The Role of Pro-Resolving Lipid Mediators in Colorectal Cancer-Associated Inflammation: Implications for Therapeutic Strategies

Overview
Journal Cancers (Basel)
Publisher MDPI
Specialty Oncology
Date 2020 Jul 30
PMID 32722560
Citations 5
Authors
Affiliations
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Abstract

Inflammation is a recognized hallmark of cancer that contributes to the development and progression of colorectal cancer (CRC). Anti-inflammatory drugs currently used for the treatment of CRC show many adverse side effects that prompted researchers to propose the polyunsaturated fatty acids-derived specialized pro-resolving mediators (SPMs) as promoters of resolution of cancer-associated inflammation. SPMs were found to inhibit the CRC-associated pro-inflammatory milieu via specific G-coupled protein receptors, although clinical data are still lacking. This review aims to summarize the state-of-the-art in this field, ultimately providing insights for the development of innovative anti-CRC therapies that promote the endogenous lipid-mediated resolution of CRC-associated inflammation.

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References
1.
Gupta R, DuBois R . Colorectal cancer prevention and treatment by inhibition of cyclooxygenase-2. Nat Rev Cancer. 2002; 1(1):11-21. DOI: 10.1038/35094017. View

2.
Le Gouvello S, Bastuji-Garin S, Aloulou N, Mansour H, Chaumette M, Berrehar F . High prevalence of Foxp3 and IL17 in MMR-proficient colorectal carcinomas. Gut. 2007; 57(6):772-9. DOI: 10.1136/gut.2007.123794. View

3.
Tacconi C, Correale C, Gandelli A, Spinelli A, Dejana E, DAlessio S . Vascular endothelial growth factor C disrupts the endothelial lymphatic barrier to promote colorectal cancer invasion. Gastroenterology. 2015; 148(7):1438-51.e8. DOI: 10.1053/j.gastro.2015.03.005. View

4.
Wang W, Yang J, Nimiya Y, Lee K, Sanidad K, Qi W . ω-3 Polyunsaturated fatty acids and their cytochrome P450-derived metabolites suppress colorectal tumor development in mice. J Nutr Biochem. 2017; 48:29-35. PMC: 6278818. DOI: 10.1016/j.jnutbio.2017.06.006. View

5.
Soehnlein O, Lindbom L . Phagocyte partnership during the onset and resolution of inflammation. Nat Rev Immunol. 2010; 10(6):427-39. DOI: 10.1038/nri2779. View