Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/17492
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dc.contributor.authorRussell, Nicholas-
dc.contributor.authorCheung, Ada S-
dc.contributor.authorGrossmann, Mathis-
dc.date2017-06-30-
dc.date.accessioned2018-04-22T23:56:47Z-
dc.date.available2018-04-22-
dc.date.issued2017-08-
dc.identifier.citationEndocrine-Related Cancer 2017; 24(8): R297-R313en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/17492-
dc.description.abstractProstate cancer (PCa) is the second most commonly diagnosed cancer in men. Conventional endocrine treatment for PCa leads to global sex steroid deprivation. The ensuing severe hypogonadism is associated with well-documented adverse effects. Recently, it has become apparent that many of the biological actions attributed to androgens in men are in fact not direct, but mediated by estradiol. Available evidence supports a primary role for estradiol in vasomotor stability, skeletal maturation and maintenance, and prevention of fat accumulation. Hence there has been interest in revisiting estradiol as a treatment for PCa. Potential roles for estradiol could be in lieu of conventional androgen deprivation therapy or as low-dose add-back treatment while continuing androgen deprivation therapy. These strategies may limit some of the side effects associated with conventional androgen deprivation therapy. However, although available data are reassuring, the potential for cardiovascular risk and pro-carcinogenic effects on PCa via estrogen receptor signalling must be considered.en_US
dc.language.isoeng-
dc.subjectandrogenen_US
dc.subjectendocrine therapyen_US
dc.subjectestrogenen_US
dc.subjectprostateen_US
dc.subjecttestosteroneen_US
dc.titleEstradiol for the mitigation of adverse effects of androgen deprivation therapy.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleEndocrine-Related Canceren_US
dc.identifier.affiliationEndocrinologyen_US
dc.identifier.affiliationGeneral Medicineen_US
dc.identifier.doi10.1530/ERC-17-0153en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0001-5257-5525en_US
dc.identifier.orcid0000-0001-8261-3457en_US
dc.identifier.pubmedid28667081-
dc.type.austinJournal Article-
dc.type.austinReview-
local.name.researcherCheung, Ada S
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptEndocrinology-
crisitem.author.deptEndocrinology-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptEndocrinology-
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