Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/34479
Title: Expression of an oestrogen receptor-related antigen in human endometrium: A microphotometric study.
Authors: Anderson D.C.;Robertson W.R.;Critchley H.O.D.;Buckley C.H.
Institution: (Critchley, Buckley, Anderson, Robertson) Department of Obstetrics and Gynaecology, Monash Medical Centre, Clayton, Melbourne, Vic. 3168 Australia
Issue Date: 24-Oct-2012
Copyright year: 1992
Publisher: Oxford University Press (Great Clarendon Street, Oxford OX2 6DP, United Kingdom)
Place of publication: United Kingdom
Publication information: Human Reproduction. 7 (2) (pp 151-155), 1992. Date of Publication: 1992.
Abstract: The expression of an oestrogen receptor-related antigen has been measured by microspectrophotometry in the glandular epithelium and stroma of tissue sections from endometrial biopsies of women administered exogenous replacement of sex steroids because of premature ovarian failure. We have demonstrated that previously dormant endometrium is capable of expressing an antigen related to oestrogen receptors and that its distribution is influenced by the sex steroid environment. Immunohistochemical staining was more intense (P<0.001) in the glandular compared to the stromal cells in tissue exposed solely to oestradiol. With the administration of progesterone, the stromal staining intensity increased (P<0.0001) and that of the glandular staining decreased (P<0.0001). No assumption, however, has been made to infer that colour is stoichiometrically related to the concentration of antigen present. Further validation of immunohistochemical procedures is required because histological localization and measurement of immunohistochemical staining may be straightforward, but its relationship to antigen concentration remains unproven.
PubMed URL: 1577925 [http://www.ncbi.nlm.nih.gov/pubmed/?term=1577925]
ISSN: 0268-1161
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/34479
Type: Article
Appears in Collections:Articles

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