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Article: Stem cells and aberrant signaling of molecular systems in skin aging

TitleStem cells and aberrant signaling of molecular systems in skin aging
Authors
KeywordsEstrogen deficiency
ROS damage
Skin aging
Skin stem/progenitor cells
Telomere shortening
Issue Date2015
PublisherElsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/arr
Citation
Ageing Research Reviews, 2015, v. 19, p. 8-21 How to Cite?
AbstractThe skin is the body's largest organ and it is able to self-repair throughout an individual's life. With advanced age, skin is prone to degenerate in response to damage. Although cosmetic surgery has been widely adopted to rejuvinate skin, we are far from a clear understanding of the mechanisms responsible for skin aging. Recently, adult skin-resident stem/progenitor cells, growth arrest, senescence or apoptotic death and dysfunction caused by alterations in key signaling genes, such as Ras/Raf/MEK/ERK, PI3K/Akt-kinases, Wnt, p21 and p53, have been shown to play a vital role in skin regeneration. Simultaneously, enhanced telomere attrition, hormone exhaustion, oxidative stress, genetic events and ultraviolet radiation exposure that result in severe DNA damage, genomic instability and epigenetic mutations also contribute to skin aging. Therefore, cell replacement and targeting of the molecular systems found in skin hold great promise for controlling or even curing skin aging. Copyright © 2014 Elsevier B.V. All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/210765
ISSN
2021 Impact Factor: 11.788
2020 SCImago Journal Rankings: 3.523
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorPENG, Y-
dc.contributor.authorXuan, M-
dc.contributor.authorLeung, VYL-
dc.contributor.authorCheng, B-
dc.date.accessioned2015-06-23T05:49:56Z-
dc.date.available2015-06-23T05:49:56Z-
dc.date.issued2015-
dc.identifier.citationAgeing Research Reviews, 2015, v. 19, p. 8-21-
dc.identifier.issn1568-1637-
dc.identifier.urihttp://hdl.handle.net/10722/210765-
dc.description.abstractThe skin is the body's largest organ and it is able to self-repair throughout an individual's life. With advanced age, skin is prone to degenerate in response to damage. Although cosmetic surgery has been widely adopted to rejuvinate skin, we are far from a clear understanding of the mechanisms responsible for skin aging. Recently, adult skin-resident stem/progenitor cells, growth arrest, senescence or apoptotic death and dysfunction caused by alterations in key signaling genes, such as Ras/Raf/MEK/ERK, PI3K/Akt-kinases, Wnt, p21 and p53, have been shown to play a vital role in skin regeneration. Simultaneously, enhanced telomere attrition, hormone exhaustion, oxidative stress, genetic events and ultraviolet radiation exposure that result in severe DNA damage, genomic instability and epigenetic mutations also contribute to skin aging. Therefore, cell replacement and targeting of the molecular systems found in skin hold great promise for controlling or even curing skin aging. Copyright © 2014 Elsevier B.V. All rights reserved.-
dc.languageeng-
dc.publisherElsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/arr-
dc.relation.ispartofAgeing Research Reviews-
dc.subjectEstrogen deficiency-
dc.subjectROS damage-
dc.subjectSkin aging-
dc.subjectSkin stem/progenitor cells-
dc.subjectTelomere shortening-
dc.titleStem cells and aberrant signaling of molecular systems in skin aging-
dc.typeArticle-
dc.identifier.emailLeung, VYL: vicleung@hku.hk-
dc.identifier.authorityLeung, VYL=rp01764-
dc.identifier.doi10.1016/j.arr.2014.10.006-
dc.identifier.pmid25446806-
dc.identifier.scopuseid_2-s2.0-84911910450-
dc.identifier.hkuros244031-
dc.identifier.volume19-
dc.identifier.spage8-
dc.identifier.epage21-
dc.identifier.isiWOS:000347868000002-
dc.publisher.placeIreland-
dc.identifier.issnl1568-1637-

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