File Download
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.3390/ijms22179386
- Scopus: eid_2-s2.0-85113847288
- PMID: 34502295
- WOS: WOS:000694273800001
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: A-FABP in Metabolic Diseases and the Therapeutic Implications: An Update
Title | A-FABP in Metabolic Diseases and the Therapeutic Implications: An Update |
---|---|
Authors | |
Keywords | A-FABP metabolic syndrome cardiovascular diseases |
Issue Date | 2021 |
Publisher | Molecular 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? |
Abstract | Adipocyte 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 Identifier | http://hdl.handle.net/10722/304448 |
ISSN | 2023 Impact Factor: 4.9 2023 SCImago Journal Rankings: 1.179 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Li, HL | - |
dc.contributor.author | Wu, X | - |
dc.contributor.author | Xu, A | - |
dc.contributor.author | Hoo, RLC | - |
dc.date.accessioned | 2021-09-23T09:00:11Z | - |
dc.date.available | 2021-09-23T09:00:11Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | International Journal of Molecular Sciences, 2021, v. 22 n. 17, p. article no. 9386 | - |
dc.identifier.issn | 1661-6596 | - |
dc.identifier.uri | http://hdl.handle.net/10722/304448 | - |
dc.description.abstract | Adipocyte 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.language | eng | - |
dc.publisher | Molecular Diversity Preservation International. The Journal's web site is located at http://www.mdpi.org/ijms | - |
dc.relation.ispartof | International Journal of Molecular Sciences | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | A-FABP | - |
dc.subject | metabolic syndrome | - |
dc.subject | cardiovascular diseases | - |
dc.title | A-FABP in Metabolic Diseases and the Therapeutic Implications: An Update | - |
dc.type | Article | - |
dc.identifier.email | Wu, X: raxpwu@hku.hk | - |
dc.identifier.email | Xu, A: amxu@hkucc.hku.hk | - |
dc.identifier.email | Hoo, RLC: rubyhoo@hkucc.hku.hk | - |
dc.identifier.authority | Xu, A=rp00485 | - |
dc.identifier.authority | Hoo, RLC=rp01334 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.3390/ijms22179386 | - |
dc.identifier.pmid | 34502295 | - |
dc.identifier.pmcid | PMC8456319 | - |
dc.identifier.scopus | eid_2-s2.0-85113847288 | - |
dc.identifier.hkuros | 325693 | - |
dc.identifier.volume | 22 | - |
dc.identifier.issue | 17 | - |
dc.identifier.spage | article no. 9386 | - |
dc.identifier.epage | article no. 9386 | - |
dc.identifier.isi | WOS:000694273800001 | - |
dc.publisher.place | Switzerland | - |