Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/8223
Title: Pituitary hyperplasia, hormonal changes and prolactinoma development in males exposed to estrogens—an insight from translational studies
Authors: Šošić-Jurjević, Branka
Ajdžanovic V.
Miljic D.
Trifunović S.
Filipović B.
Sanja S.
Bolevich, Sergey
Jakovljevic, Vladimir
Milosević V.
Issue Date: 2020
Abstract: © 2020 by the authors. Licensee MDPI, Basel, Switzerland. Estrogen signaling plays an important role in pituitary development and function. In sensitive rat or mice strains of both sexes, estrogen treatments promote lactotropic cell proliferation and induce the formation of pituitary adenomas (dominantly prolactin or growth-hormone-secreting ones). In male patients receiving estrogen, treatment does not necessarily result in pituitary hyperplasia, hyperprolactinemia or adenoma development. In this review, we comprehensively analyze the mechanisms of estrogen action upon their application in male animal models comparing it with available data in human subjects. Sex-specific molecular targets of estrogen action in lactotropic (PRL) cells are highlighted in the context of their proliferative and secretory activity. In addition, putative effects of estradiol on the cellular/tumor microenvironment and the contribution of postnatal pituitary progenitor/stem cells and transdifferentiation processes to prolactinoma development have been analyzed. Finally, estrogen-induced morphological and hormone-secreting changes in pituitary thyrotropic (TSH) and adrenocorticotropic (ACTH) cells are discussed, as well as the putative role of the thyroid and/or glucocorticoid hormones in prolactinoma development, based on the current scarce literature.
URI: https://scidar.kg.ac.rs/handle/123456789/8223
Type: review
DOI: 10.3390/ijms21062024
ISSN: 1661-6596
SCOPUS: 2-s2.0-85082087099
Appears in Collections:Faculty of Medical Sciences, Kragujevac

Page views(s)

538

Downloads(s)

26

Files in This Item:
File Description SizeFormat 
10.3390-ijms21062024.pdf3.9 MBAdobe PDFThumbnail
View/Open


This item is licensed under a Creative Commons License Creative Commons