Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/10682
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dc.contributor.authorChow, Laurie T Cen
dc.contributor.authorRezmann, Linda Adrianaen
dc.contributor.authorCatt, K Jen
dc.contributor.authorLouis, William Jen
dc.contributor.authorFrauman, Albert Gen
dc.contributor.authorNahmias, Cen
dc.contributor.authorLouis, Simon N Sen
dc.date.accessioned2015-05-16T00:12:48Z
dc.date.available2015-05-16T00:12:48Z
dc.date.issued2008-09-07en
dc.identifier.citationMolecular and Cellular Endocrinology 2008; 302(2): 219-29en
dc.identifier.govdoc18824067en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/10682en
dc.description.abstractProstate cancer is highly prevalent in Western society, and its early stages can be controlled by androgen ablation therapy. However, the cancer eventually regresses to an androgen-independent state for which there is no effective treatment. The renin-angiotensin system (RAS), in particular the octapeptide angiotensin II, is now recognised to have important effects on growth factor signalling and cell growth in addition to its well known actions on blood pressure, fluid homeostasis and electrolyte balance. All components of the RAS have been recently identified in the prostate, consistent with the expression of a local RAS system in this tissue. This review focuses on the role of the RAS in the prostate, and the possibility that this pathway may be a potential therapeutic target for the treatment of prostate cancer and other prostatic diseases.en
dc.language.isoenen
dc.subject.otherHumansen
dc.subject.otherMaleen
dc.subject.otherProstate.chemistryen
dc.subject.otherProstatic Neoplasms.drug therapy.metabolismen
dc.subject.otherReceptors, Angiotensin.drug effectsen
dc.subject.otherRenin-Angiotensin System.drug effects.physiologyen
dc.titleRole of the renin-angiotensin system in prostate cancer.en
dc.typeJournal Articleen
dc.identifier.journaltitleMolecular and cellular endocrinologyen
dc.identifier.affiliationUniversity of Melbourne, Department of Medicine, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.doi10.1016/j.mce.2008.08.032en
dc.description.pages219-29en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/18824067en
dc.type.austinJournal Articleen
local.name.researcherFrauman, Albert G
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.cerifentitytypePublications-
crisitem.author.deptClinical Pharmacology and Therapeutics-
crisitem.author.deptClinical Pharmacology and Therapeutics-
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