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Article: A-FABP in Metabolic Diseases and the Therapeutic Implications: An Update

TitleA-FABP in Metabolic Diseases and the Therapeutic Implications: An Update
Authors
KeywordsA-FABP
metabolic syndrome
cardiovascular diseases
Issue Date2021
PublisherMolecular Diversity Preservation International. The Journal's web site is located at http://www.mdpi.org/ijms
Citation
International Journal of Molecular Sciences, 2021, v. 22 n. 17, p. article no. 9386 How to Cite?
AbstractAdipocyte fatty acid-binding protein (A-FABP), which is also known as ap2 or FABP4, is a fatty acid chaperone that has been further defined as a fat-derived hormone. It regulates lipid homeostasis and is a key mediator of inflammation. Circulating levels of A-FABP are closely associated with metabolic syndrome and cardiometabolic diseases with imminent diagnostic and prognostic significance. Numerous animal studies have elucidated the potential underlying mechanisms involving A-FABP in these diseases. Recent studies demonstrated its physiological role in the regulation of adaptive thermogenesis and its pathological roles in ischemic stroke and liver fibrosis. Due to its implication in various diseases, A-FABP has become a promising target for the development of small molecule inhibitors and neutralizing antibodies for disease treatment. This review summarizes the clinical and animal findings of A-FABP in the pathogenesis of cardio-metabolic diseases in recent years. The underlying mechanism and its therapeutic implications are also highlighted.
Persistent Identifierhttp://hdl.handle.net/10722/304448
ISSN
2011 Impact Factor: 2.598
2020 SCImago Journal Rankings: 1.455
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLi, HL-
dc.contributor.authorWu, X-
dc.contributor.authorXu, A-
dc.contributor.authorHoo, RLC-
dc.date.accessioned2021-09-23T09:00:11Z-
dc.date.available2021-09-23T09:00:11Z-
dc.date.issued2021-
dc.identifier.citationInternational Journal of Molecular Sciences, 2021, v. 22 n. 17, p. article no. 9386-
dc.identifier.issn1661-6596-
dc.identifier.urihttp://hdl.handle.net/10722/304448-
dc.description.abstractAdipocyte fatty acid-binding protein (A-FABP), which is also known as ap2 or FABP4, is a fatty acid chaperone that has been further defined as a fat-derived hormone. It regulates lipid homeostasis and is a key mediator of inflammation. Circulating levels of A-FABP are closely associated with metabolic syndrome and cardiometabolic diseases with imminent diagnostic and prognostic significance. Numerous animal studies have elucidated the potential underlying mechanisms involving A-FABP in these diseases. Recent studies demonstrated its physiological role in the regulation of adaptive thermogenesis and its pathological roles in ischemic stroke and liver fibrosis. Due to its implication in various diseases, A-FABP has become a promising target for the development of small molecule inhibitors and neutralizing antibodies for disease treatment. This review summarizes the clinical and animal findings of A-FABP in the pathogenesis of cardio-metabolic diseases in recent years. The underlying mechanism and its therapeutic implications are also highlighted.-
dc.languageeng-
dc.publisherMolecular Diversity Preservation International. The Journal's web site is located at http://www.mdpi.org/ijms-
dc.relation.ispartofInternational Journal of Molecular Sciences-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectA-FABP-
dc.subjectmetabolic syndrome-
dc.subjectcardiovascular diseases-
dc.titleA-FABP in Metabolic Diseases and the Therapeutic Implications: An Update-
dc.typeArticle-
dc.identifier.emailWu, X: raxpwu@hku.hk-
dc.identifier.emailXu, A: amxu@hkucc.hku.hk-
dc.identifier.emailHoo, RLC: rubyhoo@hkucc.hku.hk-
dc.identifier.authorityXu, A=rp00485-
dc.identifier.authorityHoo, RLC=rp01334-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.3390/ijms22179386-
dc.identifier.pmid34502295-
dc.identifier.pmcidPMC8456319-
dc.identifier.scopuseid_2-s2.0-85113847288-
dc.identifier.hkuros325693-
dc.identifier.volume22-
dc.identifier.issue17-
dc.identifier.spagearticle no. 9386-
dc.identifier.epagearticle no. 9386-
dc.identifier.isiWOS:000694273800001-
dc.publisher.placeSwitzerland-

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