Genes Differentially Expressed in Prolactinomas Responsive and Resistant to Dopamine Agonists

被引:56
作者
Passos, Vanessa Q. [1 ]
Fortes, Maria Angela H. Z. [2 ]
Giannella-Neto, Daniel [2 ]
Bronstein, Marcello D. [1 ]
机构
[1] Univ Sao Paulo, Sch Med, Div Endocrinol & Metab, Neuroendocrine Unit,Hosp Clin, Sao Paulo, Brazil
[2] Univ Sao Paulo, Sch Med, Hosp Clin, Lab Cellular & Mol Endocrinol LIM 25, Sao Paulo, Brazil
关键词
Prolactinoma; Dopamine agonist; Gene expression; Estrogen receptor; Pituitary tumor transforming gene; TUMOR-TRANSFORMING GENE; NERVE GROWTH-FACTOR; PITUITARY-CELLS; LONG-TERM; BROMOCRIPTINE; CABERGOLINE; ESTROGEN; PTTG; MACROPROLACTINOMA; TUMORIGENESIS;
D O I
10.1159/000156116
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Aims: Prolactin (PRL) secretion and its gene expression are inhibited by dopamine. Prolactinomas are the most common secreting pituitary adenomas, and dopamine agonists (DA) are the first choice for their treatment. However, a subset of patients is resistant to DA. As the mechanisms involved in DA resistance are not fully understood, the aim of this study was to obtain new insights regarding the molecular differences between the prolactinomas that are responsive to DA and those that are resistant. Methods: Tumor tissue samples were collected from 17 patients who harbored prolactinomas, which were classified as responsive or resistant according to their clinical and laboratorial reaction to DA. The expression of 6 genes was evaluated by real-time polymerase chain reaction: dopamine receptor type 2 (DRD 2), nerve growth factor-beta (NGFB) and its receptor (NGFR), estrogen receptor-alpha (ERA), estrogen receptor-beta (ERB) and the pituitary tumor transforming gene (PTTG). Results: Median DRD 2 and NGFR expression in responsive patients was significantly higher than in resistant ones (p = 0.029 and p = 0.020, respectively). Moreover, the expressions of DRD 2 and NGFR were positively correlated with PRL decrease during treatment (r = 0.66, p = 0.005 and r = 0.57, p = 0.044, respectively). Furthermore, ERB expression was positively correlated to PTTG expression (r = 0.68, p = 0.032) and negatively correlated to NGFB expression (r = -0.75, p = 0.02). Conclusions: DRD2 and NGFR expressions are related to the responsiveness of prolactinoma to DA. However, PTTG, ERB and ERA expressions are not. Also ERB, ERA and PTTG expressions did not present a clear correlation to tumor aggressiveness. Furthermore, the response of prolactinomas to DA should be viewed as a spectrum ranging from the most responsive to the most resistant ones. Copyright (c) 2008 S. Karger AG, Basel
引用
收藏
页码:163 / 170
页数:8
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