Literature DB >> 12638719

Expression of aromatase P450 is increased in spontaneous prolactinomas of aged rats.

José Carretero1, Deborah Jane Burks, Gabriel Vázquez, Manuel Rubio, Elena Hernández, Pilar Bodego, Ricardo Vázquez.   

Abstract

We have recently reported the presence of aromatase P450 in the rat hypophysis. This enzyme is responsible for the aromatization of testosterone to estradiol. Since the induction of prolactinomas has been demonstrated in the rat following chronic treatment with estradiol, the aim of the present study was to analyze whether a relationship exists between the presence of pituitary aromatase and the appearance of spontaneous prolactinomas in aged rats. Of a series of 90 adenomas studied, 53% showed prolactin immunoreactive cells and were classified as prolactinomas; only 33% of the adenomas were pure prolactinomas and the other 20% were multi-hormonal protactinomas. Moreover, 60% of the adenomas were aromatase-positive tumors. Interestingly, 100% of the pure prolactinomas were aromatase-positive while only 60% of the multi-hormonal prolactinomas expressed the enzyme. Western blotting with anti-aromatase antibodies revealed a 3.8-fold increase in expression of aromatase in pituitary tumors as compared to normal rat pituitary gland. Double immunohistochemical labeling detected the coexistence of prolactin and aromatase P450 in prolactinoma cells. ACTH- and LH-positive adenomas were considered as controls; only multi-hormonal ACTH and LH tumors display aromatase-positive cells and all of these also contained prolactin-positive cells. Our results demonstrate for the first time that aromatase is expressed in pituitary adenomas and that it is related to the functional nature of the tumor, especially in the case of pure prolactinomas, suggesting the possibility that an abnormally high conversion of testosterone into estradiol in pituitary cells may contribute to the genesis of spontaneous prolactinomas in aged rats.

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Year:  2002        PMID: 12638719     DOI: 10.1023/a:1022176631922

Source DB:  PubMed          Journal:  Pituitary        ISSN: 1386-341X            Impact factor:   4.107


  27 in total

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5.  Immunohistochemical evidence of the presence of aromatase P450 in the rat hypophysis.

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Journal:  Cell Tissue Res       Date:  1999-03       Impact factor: 5.249

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Journal:  Brain Res       Date:  1994-02-28       Impact factor: 3.252

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Journal:  Am J Pathol       Date:  1991-09       Impact factor: 4.307

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Authors:  V Herman; J Fagin; R Gonsky; K Kovacs; S Melmed
Journal:  J Clin Endocrinol Metab       Date:  1990-12       Impact factor: 5.958

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3.  Localization of the aromatase enzyme expression in the human pituitary gland and its effect on growth hormone, prolactin, and thyroid stimulating hormone axis.

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Journal:  Endocrine       Date:  2015-02-20       Impact factor: 3.633

4.  Locally produced estrogen through aromatization might enhance tissue expression of pituitary tumor transforming gene and fibroblast growth factor 2 in growth hormone-secreting adenomas.

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5.  Aromatase cytochrome P450 enzyme expression in prolactinomas and its relationship to tumor behavior.

Authors:  Hakan Akinci; Aysegul Kapucu; Kadriye Akgun Dar; Ozlem Celik; Banu Tutunculer; Gozde Sirin; Buge Oz; Nurperi Gazioglu; Haluk Ince; Süheyla Aliustaoglu; Pinar Kadioglu
Journal:  Pituitary       Date:  2013-09       Impact factor: 4.107

6.  Aromatase cytochrome P450 enzyme expression in human pituitary.

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Review 7.  What can we learn from rodents about prolactin in humans?

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8.  Local transformations of androgens into estradiol by aromatase P450 is involved in the regulation of prolactin and the proliferation of pituitary prolactin-positive cells.

Authors:  María José García Barrado; Enrique J Blanco; Marta Carretero Hernández; María Carmen Iglesias Osma; Manuel Carretero; Julio J Herrero; Deborah Jane Burks; José Carretero
Journal:  PLoS One       Date:  2014-06-30       Impact factor: 3.240

Review 9.  Relation among Aromatase P450 and Tumoral Growth in Human Prolactinomas.

Authors:  María José García-Barrado; Enrique J Blanco; María Carmen Iglesias-Osma; Marta Carretero-Hernández; Leonardo Catalano-Iniesta; Virginia Sanchez-Robledo; Manuel Carretero; Julio Joaquín Herrero; Sixto Carrero; José Carretero
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  9 in total

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