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      Lipoprotein‐associated phospholipase A2: The story continues

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          Abstract

          Inflammation is thought to play an important role in the pathogenesis of vascular diseases. Lipoprotein‐associated phospholipase A2 (Lp‐PLA2) mediates vascular inflammation through the regulation of lipid metabolism in blood, thus, it has been extensively investigated to identify its role in vascular inflammation‐related diseases, mainly atherosclerosis. Although darapladib, the most advanced Lp‐PLA2 inhibitor, failed to meet the primary endpoints of two large phase III trials in atherosclerosis patients cotreated with standard medical care, the research on Lp‐PLA2 has not been terminated. Novel pathogenic, epidemiologic, genetic, and crystallographic studies regarding Lp‐PLA2 have been reported recently, while novel inhibitors were identified through a fragment‐based lead discovery strategy. More strikingly, recent clinical and preclinical studies revealed that Lp‐PLA2 inhibition showed promising therapeutic effects in diabetic macular edema and Alzheimer's disease. In this review, we not only summarized the knowledge of Lp‐PLA2 established in the past decades but also emphasized new findings in recent years. We hope this review could be valuable for helping researchers acquire a much deeper insight into the nature of Lp‐PLA2, identify more potent and selective Lp‐PLA2 inhibitors, and discover the potential indications of Lp‐PLA2 inhibitors.

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          Proresolving lipid mediators and mechanisms in the resolution of acute inflammation.

          Inflammatory responses, like all biological cascades, are shaped by a delicate balance between positive and negative feedback loops. It is now clear that in addition to positive and negative checkpoints, the inflammatory cascade rather unexpectedly boasts an additional checkpoint, a family of chemicals that actively promote resolution and tissue repair without compromising host defense. Indeed, the resolution phase of inflammation is just as actively orchestrated and carefully choreographed as its induction and inhibition. In this review, we explore the immunological consequences of omega-3-derived specialized proresolving mediators (SPMs) and discuss their place within what is currently understood of the role of the arachidonic acid-derived prostaglandins, lipoxins, and their natural C15-epimers. We propose that treatment of inflammation should not be restricted to the use of inhibitors of the acute cascade (antagonism) but broadened to take account of the enormous therapeutic potential of inducers (agonists) of the resolution phase of inflammation.
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            Phospholipase A2 enzymes: physical structure, biological function, disease implication, chemical inhibition, and therapeutic intervention.

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              Resolution of inflammation: a new therapeutic frontier.

              Dysregulated inflammation is a central pathological process in diverse disease states. Traditionally, therapeutic approaches have sought to modulate the pro- or anti-inflammatory limbs of inflammation, with mixed success. However, insight into the pathways by which inflammation is resolved has highlighted novel opportunities to pharmacologically manipulate these processes - a strategy that might represent a complementary (and perhaps even superior) therapeutic approach. This Review discusses the state of the art in the biology of resolution of inflammation, highlighting the opportunities and challenges for translational research in this field.
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                Author and article information

                Contributors
                kwang@simm.ac.cn
                jhshen@simm.ac.cn
                Journal
                Med Res Rev
                Med Res Rev
                10.1002/(ISSN)1098-1128
                MED
                Medicinal Research Reviews
                John Wiley and Sons Inc. (Hoboken )
                0198-6325
                1098-1128
                29 May 2019
                January 2020
                : 40
                : 1 ( doiID: 10.1002/med.v40.1 )
                : 79-134
                Affiliations
                [ 1 ] State Key Laboratory of Drug Research Shanghai Institute of Materia Medica (SIMM), Chinese Academy of Sciences Shanghai China
                [ 2 ] School of Pharmacy University of Chinese Academy of Sciences Beijing China
                Author notes
                [*] [* ] Correspondence Kai Wang and Jianhua Shen, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica (SIMM), Chinese Academy of Sciences, 555 Zuchongzhi Road, 201203 Shanghai, China. Email: kwang@ 123456simm.ac.cn (KW); jhshen@ 123456simm.ac.cn (JS)

                Author information
                http://orcid.org/0000-0002-8654-7327
                Article
                MED21597
                10.1002/med.21597
                6973114
                31140638
                f6ea9936-15d0-4acc-bf9d-f5b2038c5f7f
                © 2019 The Authors. Medicinal Research Reviews Published by Wiley Periodicals, Inc.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 28 November 2018
                : 20 April 2019
                : 30 April 2019
                Page count
                Figures: 16, Tables: 1, Pages: 56, Words: 32916
                Funding
                Funded by: Shanghai Committee of Science and Technology, China
                Award ID: 18431901000
                Funded by: National Natural Science Foundation of China , open-funder-registry 10.13039/501100001809;
                Award ID: 81673302
                Award ID: 81602963
                Funded by: National Science & Technology Major Project 'Key New Drug Creation and Manufacturing Program', China
                Award ID: 2018ZX09711002‐006‐014
                Categories
                Review Article
                Review Articles
                Custom metadata
                2.0
                January 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.5 mode:remove_FC converted:21.01.2020

                fragment‐based lead discovery,inflammation,inhibitors,lipoprotein‐associated phospholipase a2,vascular diseases

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