Literature DB >> 8910802

Alteration of G alpha subunits mRNA levels in bromocriptine resistant prolactinomas.

L Caccavelli1, I Morange-Ramos, C Kordon, P Jaquet, A Enjalbert.   

Abstract

Patients with prolactinoma are commonly treated with the D2 dopamine agonist bromocriptine, which in most cases, normalizes prolactin (PRL) levels. However, resistance to bromocriptine has been observed in 5 to 18% of tested prolactinomas and is associated to a decrease in both D2 receptor density and mRNA levels. In this study, we used quantitative RT-PCR to investigate whether expression of G alpha proteins could be also modified in bromocriptine resistant prolactinomas. No difference in G alpha o mRNA levels or in the relative expression of G alpha s between bromocriptine sensitive and bromocriptine resistant prolactinomas was observed. In contrast, the relative expression of G alpha i2 was found to be decreased in bromocriptine resistant prolactinomas when compared to that of bromocriptine sensitive prolactinomas. Interestingly, the relative G alpha i2 expression was correlated to both bromocriptine inhibition of in vitro PRL secretion and D2 receptor mRNA levels. Bromocriptine resistance could thus result from a decrease in D2 dopamine receptors associated with a decrease in G alpha i2 expression.

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Year:  1996        PMID: 8910802     DOI: 10.1046/j.1365-2826.1996.04902.x

Source DB:  PubMed          Journal:  J Neuroendocrinol        ISSN: 0953-8194            Impact factor:   3.627


  16 in total

1.  Dopamine D2 receptor gene expression in human adenohypophysial adenomas.

Authors:  L Stefaneanu; K Kovacs; E Horvath; M Buchfelder; R Fahlbusch; L Lancranjan
Journal:  Endocrine       Date:  2001-04       Impact factor: 3.633

Review 2.  Pharmacologic resistance in prolactinoma patients.

Authors:  Mark E Molitch
Journal:  Pituitary       Date:  2005       Impact factor: 4.107

3.  Cabergoline and prolactinomas: lack of association between DRD2 polymorphisms and response to treatment.

Authors:  Cbf Bueno; E B Trarbach; M D Bronstein; A Glezer
Journal:  Pituitary       Date:  2017-06       Impact factor: 4.107

Review 4.  The pituitary TGFβ1 system as a novel target for the treatment of resistant prolactinomas.

Authors:  M Victoria Recouvreux; M Andrea Camilletti; Daniel B Rifkin; Graciela Díaz-Torga
Journal:  J Endocrinol       Date:  2015-12-23       Impact factor: 4.286

5.  Shrinkage of a PRL-secreting pituitary macroadenoma resistant to cabergoline.

Authors:  S Cannavò; L Bartolone; A Blandino; S Spinella; S Galatioto; F Trimarchi
Journal:  J Endocrinol Invest       Date:  1999-04       Impact factor: 4.256

6.  Curcumin Sensitizes Prolactinoma Cells to Bromocriptine by Activating the ERK/EGR1 and Inhibiting the AKT/GSK-3β Signaling Pathway In Vitro and In Vivo.

Authors:  Chao Tang; Junhao Zhu; Feng Yuan; Jin Yang; Xiangming Cai; Chiyuan Ma
Journal:  Mol Neurobiol       Date:  2021-08-31       Impact factor: 5.590

7.  Invasive giant prolactinoma with loss of therapeutic response to cabergoline: expression of angiogenic markers.

Authors:  María Susana Mallea-Gil; Carolina Cristina; María Inés Perez-Millan; Ana M Rodriguez Villafañe; Carolina Ballarino; Graciela Stalldecker; Damasia Becu-Villalobos
Journal:  Endocr Pathol       Date:  2009       Impact factor: 3.943

Review 8.  Dopamine resistance of prolactinomas.

Authors:  Mark E Molitch
Journal:  Pituitary       Date:  2003       Impact factor: 4.107

Review 9.  Drug resistance in pituitary tumours: from cell membrane to intracellular signalling.

Authors:  Erika Peverelli; Donatella Treppiedi; Federica Mangili; Rosa Catalano; Anna Spada; Giovanna Mantovani
Journal:  Nat Rev Endocrinol       Date:  2021-06-30       Impact factor: 43.330

Review 10.  Management of medically refractory prolactinoma.

Authors:  Mark E Molitch
Journal:  J Neurooncol       Date:  2013-10-22       Impact factor: 4.130

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