Literature DB >> 7078703

Effect of tamoxifen administration on prolactin release by invasive prolactin-secreting pituitary adenomas.

S W Lamberts, T Verleun, R Oosterom.   

Abstract

Bromocriptine treatment of patients with invasive prolactin (PRL)-secreting pituitary adenomas does not invariably result in normalization of the plasma PRL levels. We previously showed that the antiestrogenic drug tamoxifen inhibited hormone release from transplantable PRL-secreting pituitary tumors in rats. In 8 patients with invasive PRL-secreting pituitary adenomas with extrasellar extension, the effect of the administration of tamoxifen was investigated on the plasma PRL concentration and on the bromocriptine-mediated inhibition of PRL release. Treatment for 5 days with tamoxifen (20 mg/day) suppressed plasma PRL levels as measured in 5 samples over the day significantly by 20 +/- 3% (means +/- SEM; p less than 0.01). During tamoxifen administration the inhibition of PRL secretion by 2.5 mg bromocriptine was further suppressed by 36 +/- 7%, in comparison with the plasma PRL levels after bromocriptine alone (p less than 0.01). Tamoxifen administration suppressed PRL release in patients with giant invasive PRL-secreting pituitary adenomas, and it had a slight but significant additive or potentiating effect on the bromocriptine-mediated inhibition of PRL secretion. However, despite the simultaneous administration of bromocriptine and tamoxifen, normalization of the circulating PRL levels was not reached in this type of patient.

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Year:  1982        PMID: 7078703     DOI: 10.1159/000123324

Source DB:  PubMed          Journal:  Neuroendocrinology        ISSN: 0028-3835            Impact factor:   4.914


  15 in total

Review 1.  Medical treatment of prolactinomas.

Authors:  Annamaria Colao; Silvia Savastano
Journal:  Nat Rev Endocrinol       Date:  2011-03-22       Impact factor: 43.330

Review 2.  Pharmacologic resistance in prolactinoma patients.

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

3.  ErbB receptor-driven prolactinomas respond to targeted lapatinib treatment in female transgenic mice.

Authors:  Xiaohai Liu; Maya Kano; Takako Araki; Odelia Cooper; Hidenori Fukuoka; Yukiko Tone; Masahide Tone; Shlomo Melmed
Journal:  Endocrinology       Date:  2015-01       Impact factor: 4.736

4.  Estrogen receptors in prolactinomas: a clinico-pathological study.

Authors:  G J Kaptain; N E Simmons; T D Alden; M B Lopes; M L Vance; E R Laws
Journal:  Pituitary       Date:  1999       Impact factor: 4.107

5.  Prolactinoma ErbB receptor expression and targeted therapy for aggressive tumors.

Authors:  Odelia Cooper; Adam Mamelak; Serguei Bannykh; John Carmichael; Vivien Bonert; Stephen Lim; Galen Cook-Wiens; Anat Ben-Shlomo
Journal:  Endocrine       Date:  2013-11-28       Impact factor: 3.633

6.  Temozolomide in the treatment of an invasive prolactinoma resistant to dopamine agonists.

Authors:  Lisa M Neff; Michelle Weil; Alan Cole; Thomas R Hedges; William Shucart; Donald Lawrence; Jay-Jiguang Zhu; Arthur S Tischler; Ronald M Lechan
Journal:  Pituitary       Date:  2007       Impact factor: 4.107

Review 7.  Dopamine resistance of prolactinomas.

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

Review 8.  Management of medically refractory prolactinoma.

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

9.  Identification of Tamoxifen-Resistant Breast Cancer Cell Lines and Drug Response Signature.

Authors:  Qingzhou Guan; Xuekun Song; Zhenzhen Zhang; Yizhi Zhang; Yating Chen; Jing Li
Journal:  Front Mol Biosci       Date:  2020-12-04

10.  Preventive effects of antioestrogen on mammary and pituitary tumorigenesis in rats.

Authors:  C Sumi; K Yokoro; R Matsushima
Journal:  Br J Cancer       Date:  1984-12       Impact factor: 7.640

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