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Article: Fibroblast Growth Factor 21 Mimetics for Treating Atherosclerosis
Title | Fibroblast Growth Factor 21 Mimetics for Treating Atherosclerosis |
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Authors | |
Keywords | Atherosclerosis Dyslipidemia Fibroblast growth factor 21 |
Issue Date | 2017 |
Publisher | Korean Endocrine Society. The Journal's web site is located at http://www.enm-kes.org/ |
Citation | Endocrinology and Metabolism, 2017, v. 32 n. 2, p. 145-151 How to Cite? |
Abstract | Fibroblast growth factor 21 (FGF21) is an atypical member of the FGF family. Acting in an endocrine fashion, it increases glucose uptake, modulates lipid metabolism, and sensitizes insulin response in metabolically active organs, including the liver and adipose tissue. Emerging evidence shows a strong correlation between circulating FGF21 levels and the incidence and severity of atherosclerosis. Animal studies have demonstrated a beneficial role of FGF21 in protecting against aberrant lipid profile, while recent development in FGF21 mimetics has provided further insight into the lipid-lowering effects of FGF21 signaling. The present review summarizes the physiological roles of FGF21, and discusses major breakthroughs and limitations of FGF21 mimetic-based therapeutic strategies for treating atherosclerosis. |
Persistent Identifier | http://hdl.handle.net/10722/242226 |
ISSN | 2023 Impact Factor: 3.9 2023 SCImago Journal Rankings: 1.122 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | KWOK, HM | - |
dc.contributor.author | Lam, KSL | - |
dc.date.accessioned | 2017-07-24T01:36:59Z | - |
dc.date.available | 2017-07-24T01:36:59Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | Endocrinology and Metabolism, 2017, v. 32 n. 2, p. 145-151 | - |
dc.identifier.issn | 2093-596X | - |
dc.identifier.uri | http://hdl.handle.net/10722/242226 | - |
dc.description.abstract | Fibroblast growth factor 21 (FGF21) is an atypical member of the FGF family. Acting in an endocrine fashion, it increases glucose uptake, modulates lipid metabolism, and sensitizes insulin response in metabolically active organs, including the liver and adipose tissue. Emerging evidence shows a strong correlation between circulating FGF21 levels and the incidence and severity of atherosclerosis. Animal studies have demonstrated a beneficial role of FGF21 in protecting against aberrant lipid profile, while recent development in FGF21 mimetics has provided further insight into the lipid-lowering effects of FGF21 signaling. The present review summarizes the physiological roles of FGF21, and discusses major breakthroughs and limitations of FGF21 mimetic-based therapeutic strategies for treating atherosclerosis. | - |
dc.language | eng | - |
dc.publisher | Korean Endocrine Society. The Journal's web site is located at http://www.enm-kes.org/ | - |
dc.relation.ispartof | Endocrinology and Metabolism | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Atherosclerosis | - |
dc.subject | Dyslipidemia | - |
dc.subject | Fibroblast growth factor 21 | - |
dc.title | Fibroblast Growth Factor 21 Mimetics for Treating Atherosclerosis | - |
dc.type | Article | - |
dc.identifier.email | Lam, KSL: ksllam@hku.hk | - |
dc.identifier.authority | Lam, KSL=rp00343 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.3803/EnM.2017.32.2.145 | - |
dc.identifier.scopus | eid_2-s2.0-85023204908 | - |
dc.identifier.hkuros | 273618 | - |
dc.identifier.volume | 32 | - |
dc.identifier.issue | 2 | - |
dc.identifier.spage | 145 | - |
dc.identifier.epage | 151 | - |
dc.identifier.isi | WOS:000407811300001 | - |
dc.publisher.place | Republic of Korea | - |
dc.identifier.issnl | 2093-596X | - |