Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1994-7-5
pubmed:abstractText
Forty-one human pituitary adenoma specimens were examined for the presence of estrogen receptor (ER) messenger ribonucleic acid and protein using a combination of ribonuclease protection assay, [3H] estradiol ([3H]E2) binding, and ER immunohistochemistry. ER messenger ribonucleic acid prevalence was high in PRL-immunoreactive tumors (2 of 2), moderate in GH/PRL tumors (2 of 5), and low or absent (0 of 4) in GH tumors. In the GH/PRL-immunostaining tumors, the presence of the ER was uniformly associated with elevated serum PRL levels. Among the gonadotropin-immunostaining tumors, 10 of 17 were ER positive; within this group, those with gonadotroph adenoma characteristics were ER positive, whereas those with null cell/oncocytic characteristics were ER negative. Of the tumors that did not immunostain for any known anterior pituitary hormones, 3 of 11 were ER positive. ER immunohistochemistry in 14 tumors revealed a 100% correlation with ribonuclease protection assay results, whereas [3H]E2 binding, determined in 9 tumors, showed an 87% correlation. In summary, it appears that PRL and a specific class of gonadotropin-immunostaining tumors (identifiable by specific characteristics on electron microscope) contain ER, whereas GH-immunostaining tumors are ER negative. ER expression in normal pituitary paralleled that in macroadenomas (GH, 2.3%; PRL, 50%; FSH, 70%; LH, 83%; TSH, 4%; ACTH, 1%). The ER-positive tumors represent a subset whose growth and secretory profiles may be influenced by the gonadal steroidal milieu or by pharmacological agents that affect E2 levels or ER function.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Adrenocorticotropic Hormone, http://linkedlifedata.com/resource/pubmed/chemical/Estradiol, http://linkedlifedata.com/resource/pubmed/chemical/Follicle Stimulating Hormone, http://linkedlifedata.com/resource/pubmed/chemical/Follicle Stimulating Hormone, beta..., http://linkedlifedata.com/resource/pubmed/chemical/Glycoprotein Hormones, alpha Subunit, http://linkedlifedata.com/resource/pubmed/chemical/Growth Hormone, http://linkedlifedata.com/resource/pubmed/chemical/Luteinizing Hormone, http://linkedlifedata.com/resource/pubmed/chemical/Prolactin, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Estrogen, http://linkedlifedata.com/resource/pubmed/chemical/Thyrotropin
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0021-972X
pubmed:author
pubmed:issnType
Print
pubmed:volume
78
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1497-504
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:7515390-Adenoma, pubmed-meshheading:7515390-Adrenocorticotropic Hormone, pubmed-meshheading:7515390-Estradiol, pubmed-meshheading:7515390-Follicle Stimulating Hormone, pubmed-meshheading:7515390-Follicle Stimulating Hormone, beta Subunit, pubmed-meshheading:7515390-Gene Expression, pubmed-meshheading:7515390-Glycoprotein Hormones, alpha Subunit, pubmed-meshheading:7515390-Growth Hormone, pubmed-meshheading:7515390-Humans, pubmed-meshheading:7515390-Immunohistochemistry, pubmed-meshheading:7515390-Luteinizing Hormone, pubmed-meshheading:7515390-Pituitary Gland, pubmed-meshheading:7515390-Pituitary Neoplasms, pubmed-meshheading:7515390-Prolactin, pubmed-meshheading:7515390-RNA, Messenger, pubmed-meshheading:7515390-Receptors, Estrogen, pubmed-meshheading:7515390-Reference Values, pubmed-meshheading:7515390-Thyrotropin
pubmed:year
1994
pubmed:articleTitle
Estrogen receptor expression in human pituitary: correlation with immunohistochemistry in normal tissue, and immunohistochemistry and morphology in macroadenomas.
pubmed:affiliation
Department of Internal Medicine, University of Virginia Health Sciences Center, Charlottesville 22908.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't