Literature DB >> 25536318

Dopamine 2 and somatostatin 1-5 receptors coexpression in clinically non-functioning pituitary adenomas.

F Gabalec1, M Drastikova, T Cesak, D Netuka, V Masopust, J Machac, J Marek, J Cap, M Beranek.   

Abstract

This study investigated quantitated expression of dopamine 2 receptor (D2R) and somatostatin receptors of the five types (SSTR1-SSTR5) in a large series of clinically non-functioning pituitary adenomas (CNFAs). Co-expression of these receptors in individual adenomas was studied as well as correlation between receptor types. Adenoma tissue from 198 patients who underwent surgery for CNFAs was analyzed by immunohistochemistry and quantitative real-time PCR. D2R and SSTR1-3 mRNA was expressed in all 198 adenomas. SSTR4 and SSTR5 were detectable in 85 % and 61 % of adenomas, respectively. Expression of D2R was significantly higher than that of the somatostatin receptors. The median relative expressions were as follows from highest D2R >> SSTR3 > SSTR2 > SSTR1 > SSTR5 > SSTR4. High relative expression (ratio to beta-glucuronidase mRNA > 1) of D2R was found in 60 % of tumors, high expression of SSTR1 in 7.5 %, SSTR2 in 7 %, SSTR3 in 4 % and SSTR5 in 0.5 %. The quantity of D2R correlated positively with expression of SSTR2 and SSTR3, and negatively with SSTR1 and SSTR5. Among histological adenoma types, SSTR1 was significantly higher in null-cell adenomas and SSTR3 was lower in silent corticotroph adenomas. In conclusions, in CNFAs, high expression of somatostatin receptors is much less common than that of D2R, and co-expression of both these receptors is exceptional. D2R and SSTR3 seem to be the most promising targets for pharmacological treatment.

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Year:  2014        PMID: 25536318     DOI: 10.33549/physiolres.932821

Source DB:  PubMed          Journal:  Physiol Res        ISSN: 0862-8408            Impact factor:   1.881


  6 in total

Review 1.  International Union of Basic and Clinical Pharmacology. CV. Somatostatin Receptors: Structure, Function, Ligands, and New Nomenclature.

Authors:  Thomas Günther; Giovanni Tulipano; Pascal Dournaud; Corinne Bousquet; Zsolt Csaba; Hans-Jürgen Kreienkamp; Amelie Lupp; Márta Korbonits; Justo P Castaño; Hans-Jürgen Wester; Michael Culler; Shlomo Melmed; Stefan Schulz
Journal:  Pharmacol Rev       Date:  2018-10       Impact factor: 25.468

2.  TBR-760, a Dopamine-Somatostatin Compound, Arrests Growth of Aggressive Nonfunctioning Pituitary Adenomas in Mice.

Authors:  Heather A Halem; Ute Hochgeschwender; Jeong Keun Rih; Richard Nelson; G Allan Johnson; Arunthi Thiagalingam; Michael D Culler
Journal:  Endocrinology       Date:  2020-08-01       Impact factor: 4.736

Review 3.  Targeting Aggressive Pituitary Adenomas at the Molecular Level-A Review.

Authors:  Benjamin Voellger; Zhuo Zhang; Julia Benzel; Junwen Wang; Ting Lei; Christopher Nimsky; Jörg-Walter Bartsch
Journal:  J Clin Med       Date:  2021-12-27       Impact factor: 4.241

4.  68Ga-DOTATATE PET imaging in clinically non-functioning pituitary macroadenomas.

Authors:  Peter H Bisschop; Eric Fliers; Tessel M Boertien; Jan Booij; Charles B L M Majoie; Madeleine L Drent; Alberto M Pereira; Nienke R Biermasz; Suat Simsek; Ronald Groote Veldman; Marcel P M Stokkel
Journal:  Eur J Hybrid Imaging       Date:  2020-02-27

Review 5.  Dopamine Agonists for Pituitary Adenomas.

Authors:  Odelia Cooper; Yona Greenman
Journal:  Front Endocrinol (Lausanne)       Date:  2018-08-21       Impact factor: 5.555

6.  The GALANT trial: study protocol of a randomised placebo-controlled trial in patients with a 68 Ga -DOTATATE PET-positive, clinically non-functioning pituitary macroadenoma on the effect of lan reotide on t umour size.

Authors:  Eric Fliers; Peter H Bisschop; Tessel M Boertien; Madeleine L Drent; Jan Booij; Charles B L M Majoie; Marcel P M Stokkel; Jantien Hoogmoed; Alberto Pereira; Nienke R Biermasz; Suat Simsek; Ronald Groote Veldman; Michael W T Tanck
Journal:  BMJ Open       Date:  2020-08-13       Impact factor: 2.692

  6 in total

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