Immunohistochemical study of somatostatin and dopamine receptors (SSTR2, SSTR5, DR2) in pituitary adenomas to justify targeted therapy

封面

如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅或者付费存取

详细

Introduction. Adenomas are the most common disease affecting the pituitary gland. Most of these tumors can be successfully treated. The main method is transsphenoidal resection. The exception is prolactinomas, which are treated with dopamine agonists.

Objective. Analysis of DR2, SSTR2, SSTR5 expression in various adenomas and normal adenohypophysis to justify targeted therapy.

Material and methods. Histological and immunohistochemical examination of surgical material from 42 pituitary adenomas and 6 pituitary glands without pathology (autopsy) with SSTR2, SSTR5, DR2 markers, ACTH, PRL, GH, FSH, LH, TSH hormones. Of these, 22 prolactinomas of patients undergoing preoperative treatment with cabergoline, 10 corticotropin, 10 zero-cell adenomas; 6 pituitary glands without pathology (control group). Receptor expression was assessed in points from 1 to 4.

Results. DR2 were expressed in 39 of 42 adenomas and in all 6 normal adenohypophysis; SSTR2 – in 12 adenomas and all normal adenohypophysis, SSTR5 – in 29 and 6, respectively. Statistical analysis did not reveal a significant difference in DR2 expression in different types of adenomas; in prolactinomas and normal adenohypophysis; in the level of SSTR2 and SSTR5 expression in corticotropinomas and normal adenohypophysis; SSTR5 and DR2 in a group with 19 prolactinomas, 2 mammosomatropinomas, 1 plurihormonal adenoma (the last 3 were considered by clinicians as prolactinomas).

Conclusion. There is no significant difference in DR2 expression in patients with prolactinomas, zero-cell adenomas, and corticotropinomas, which raises questions about the feasibility of dopamine agonist therapy only in patients with hyperprolactinemia.

There is no significant difference in DR2 and SSTR5 expression in prolactinomas, which indicates the possibility of alternative therapy with somatostatin receptor analogs.

The pronounced expression of DR2, SSTR2, and SSTR5 not only in pituitary adenomas but also in the normal adenohypophysis raises questions about the adverse effects on unchanged adenomeres and also requires larger-scale studies.

全文:

受限制的访问

作者简介

Ksenia Guseva

Federal State Budgetary Institution «V.A. Almazov National Medical Research Centre» of the Ministry of Health of the Russian Federation

编辑信件的主要联系方式.
Email: ksuha.gus@yandex.ru
ORCID iD: 0009-0009-4477-9128
SPIN 代码: 8344-2560

Clinical resident of the Department of Pathological Anatomy with clinic

俄罗斯联邦, st. Akkuratova, 2, Saint-Petersburg, 197341

Artem Paltsev

Federal State Budgetary Institution «V.A. Almazov National Medical Research Centre» of the Ministry of Health of the Russian Federation

Email: Artem.paltsev@gmail.com
ORCID iD: 0000-0002-9966-2965
SPIN 代码: 9944-1407

Head of the Department of Neurosurgery No. 6

俄罗斯联邦, st. Akkuratova, 2, Saint-Petersburg, 197341

Lyubov Mitrofanova

Federal State Budgetary Institution «V.A. Almazov National Medical Research Centre» of the Ministry of Health of the Russian Federation

Email: lubamitr@yandex.ru
ORCID iD: 0000-0003-0735-7822
SPIN 代码: 9552-8248

Head of the Department of Pathological Anatomy with Clinic, Chief Researcher of the Pathomorphology Research Laboratory, Head of the Pathomorphology Service, pathologist of the highest category of the Pathoanatomical Department of the University Clinic., Executive Secretary of the Central Attestation Commission of the Ministry of Health of the Russian Federation according to the laboratory diagnostic profile, Deputy Chairman of the Dissertation Council on 21.1.028.04 on pathological anatomy 3.3.2, Doctor of Medical Sciences, Professor

俄罗斯联邦, st. Akkuratova, 2, Saint-Petersburg, 197341

参考

  1. Yeh P.J., Chen J.W. Pituitary tumors: surgical and medical management. Surgical Oncology. 1997; 6 (2): 67–92. doi: 10.1016/s0960-7404(97)00008-x. PMID: 9436654.
  2. La Rosa S., Uccella S. Pituitary Tumors: Pathology and Genetics. Reference Module in Biomedical Sciences. 2018. doi: 10.1016/B978-0-12-801238-3.65086-9
  3. Liu X., Tang C., Wen G., Zhong C., Yang J., Zhu J., Ma C. The Mechanism and Pathways of Dopamine and Dopamine Agonists in Prolactinomas. Frontiers in Endocrinology (Lausanne). 2019; 9: 768. doi: 10.3389/fendo.2018.00768. PMID: 30740089; PMCID: PMC6357924.
  4. Asa S., Mete O., Perry A., Osamura R. Overview of the 2022 WHO Classification of Pituitary Tumors. Endocrine Pathology. 2022; 33 (1): 6–26. doi: 10.1007/s12022-022-09703-7.
  5. Fernandez A., Karavitaki N., Wass J.A. Prevalence of pituitary adenomas: a community-based, cross-sectional study in Banbury (Oxfordshire, UK). The Journal of Clinical Endocrinology (Oxford). 2010; 72 (3): 377–82. doi: 10.1111/j.1365-2265.2009.03667.
  6. Daly A.F., Beckers A. The Epidemiology of Pituitary Adenomas. Endocrinology and Metabolism Clinics of North America. 2020; 49 (3): 347–55. doi: 10.1016/j.ecl.2020.04.002
  7. Vamvoukaki R., Chrysoulaki M., Betsi G., Xekouki P. Pituitary Tumorigenesis-Implications for Management. Medicina (Kaunas). 2023; 59 (4): 812. doi: 10.3390/medicina59040812.
  8. Шутова А.С., Дзеранова Л.К., Воротникова С.Ю., Кутин МА, Пигарова Е.А. Современные представления о генетических и иммуногистохимических особенностях пролактинсекретирующих аденом гипофиза. Проблемы эндокринологии. 2023; 69 (3): 44–50. doi: 10.14341/probl13222. PMID: 37448246; PMCID: PMC10350616. [Shutova A.S., Dzeranova L.K., Vorotnikova S.Y., Kutin M.A., Pigarova E.A. Modern concepts of genetic and immunohistochemical features of prolactin-secreting pituitary adenomas. Problems of Endokrinology. 2023; 69 (3): 44–50. doi: 10.14341/probl13222. PMID: 37448246; PMCID: PMC10350616 (in Russian)]
  9. Шутова А.С., Пигарова Е.А., Лепешкина Л.И., Иоутси В.А., Дроков М.Ю., Воротникова С.Ю., Астафьева Л.И., Дзеранова Л.К. Преодоление резистентности пролактином к медикаментозной терапии: от перспектив к реальной клинической практике. Проблемы Эндокринологии. 2023; 69 (6): 63–9. doi: 10.14341/probl13351. [Shutova A.S., Pigarova E.A., Lepeshkina L.I., Ioutsi V.A., Drokov M.Yu., Vorotnikova S.Yu., Astafieva L.I., Dzeranova L.K. Overcoming prolactin resistance to drug therapy: from prospects to the implementation of clinical practice. Problems of Endocrinology. 2023; 69 (6): 63–9. doi: 10.14341/probl13351 (in Russian)]
  10. Мельниченко Г.А., Дзеранова Л.К., Пигарова Е.А., Воротникова С.Ю., Рожинская Л.Я., Дедов И.И. Федеральные клинические рекомендации по гиперпролактинемии: клиника, диагностика, дифференциальная диагностика и методы лечения. Проблемы эндокринологии. 2013; 3. DOI: 7062-11501-1. [Melnichenko G.A., Dzeranova L.K., Pigarova E.A., Vorotnikova S.Yu., Rozhinskaya L.Ya., Dedov I.I. Federal clinical guidelines for hyperprolactinemia: clinical presentation, diagnostics, differential diagnostics and treatment methods. Problems of Endocrinology. 2013; 3. DOI: 7062-11501-1 (in Russian)]
  11. Андреева А.В., Маркина Н.В., Анциферов М.Б. Современные подходы к терапии болезни Иценко-Кушинга. Проблемы Эндокринологии. 2016; 62 (4): 50–5. doi: 10.14341/probl201662450-55. [Andreeva A.V., Markina N.V., Antsiferov M.B. Modern approaches to the treatment of Itsenko-Cushing’s disease. Problems of Endocrinology. 2016; 62 (4): 50–5. doi: 10.14341/probl201662450-55 (in Russian)]
  12. Марова Е.И., Дзеранова Л.К., Воронцов А.В., Гончаров Н.П., Каменская Е.А., Беляева А.В., Бармина И.И. Перекрестное рандомизированное клиническое исследование сравнения эффективности и безопасности препаратов абергин и бромокриптин у больных с синдромом гиперпролактинемии. Проблемы Эндокринологии. 2008; 54 (5): 20–5. doi: 10.14341/probl200854520-25. [Marova E.I., Dzeranova L.K., Vorontsov A.V., Goncharov N.P., Kamenskaya E.A., Belyaeva A.V., Barmina I.I. Crossover randomized clinical trial comparing the efficacy and safety of abergin and bromocriptine in patients with hyperprolactinemia syndrome. Problems of Endocrinology. 2008; 54 (5): 20–5. doi: 10.14341/probl200854520-25 (in Russian)]
  13. Bhatia A., Lenchner J.R., Saadabadi A. Biochemistry, Dopamine Receptors. StatPearls [Internet]. 2025. PMID: 30855830
  14. Гусева К.А., Лазарева А.А., Мацуева И.А., Пальцев А.А., Гринева Е.Н., Митрофанова Л.Б. Вызывают ли агонисты дофамина фиброз? Сравнительное морфологическое исследование различных аденом гипофиза. Медлайн.ру. 2025; 26: 142–69. [Guseva K.A., Lazareva A.A., Matsueva I.A., Pal’tsev A.A., Grineva E.N., Mitrofanova L.B. Do dopamine agonists cause fibrosis? Comparative morphological study of various pituitary adenomas. Medline.ru. 2025; 26: 142–69 (in Russian)]
  15. Liu X., Tang C., Wen G., Zhong C., Yang J., Zhu J., Ma C. The Mechanism and Pathways of Dopamine and Dopamine Agonists in Prolactinomas. Frontiers in Endocrinology (Lausanne). 2019; 9: 768. doi: 10.3389/fendo.2018.00768. PMID: 30740089; PMCID: PMC6357924.
  16. Gomes-Porras M., Cárdenas-Salas J., Álvarez-Escolá C. Somatostatin Analogs in Clinical Practice: a Review. International J. of Molecular Sciences. 2020; 21 (5): 1682. doi: 10.3390/ijms21051682. PMID: 32121432; PMCID: PMC7084228.
  17. Sawicka-Gutaj N., Owecki M., Ruchala M. Pasireotide – Mechanism of Action and Clinical Applications. Current Drug Metabolism. 2018; 19 (10): 876–82. doi: 10.2174/1389200219666180328113801. PMID: 29595102.
  18. Lasolle H., Vasiljevic A., Borson-Chazot F., Raverot G. Pasireotide: A potential therapeutic alternative for resistant prolactinoma. The Annales d’Endocrinologie (Paris). 2019; 80 (2): 84–8. doi: 10.1016/j.ando.2018.07.013.
  19. Schmid H.A. Pasireotide (SOM230): development, mechanism of action and potential applications. Molecular and Cellular Endocrinology. 2008; 286 (1–2): 69–74. doi: 10.1016/j.mce.2007.09.006. Epub 2007 Sep 19. PMID: 17977644.
  20. Coopmans E.C., van Meyel S.W.F., Pieterman K.J., van Ipenburg J.A., Hofland L.J., Donga E., Daly A.F., Beckers A., van der Lely A.J., Neggers S.J.C.M.M. Excellent response to pasireotide therapy in an aggressive and dopamine-resistant prolactinoma. European J. of Endocrinology. 2019; 181 (2): 21–7. doi: 10.1530/EJE-19-0279. PMID: 31167168.
  21. Raverot G., Vasiljevic A., Jouanneau E., Lasolle H. Confirmation of a new therapeutic option for aggressive or dopamine agonist-resistant prolactin pituitary neuroendocrine tumors. European J. of Endocrinology. 2019; 181 (2): 1–3. doi: 10.1530/EJE-19-0359. PMID: 31167164.
  22. Митрофанова Л.Б., Коновалов П.В., Крылова Ю.С., Полякова В.О., Кветной И.М. Плюригормональные клетки аденогипофиза. Новые возможности оптимизации молекулярной диагностики нейроэндокринных опухолей. Молекулярная медицина. 2017; 15 (6): 38–45. DOI: 2310.2174/1389200219666180328113801. PMID: 29595102. [Mitrofanova L.B., Konovalov P.V., Krylova Yu.S., Polyakova V.O., Kvetnoy I.M. Plurihormonal cells of the adenohypophysis. New possibilities for optimization of molecular diagnostics of neuroendocrine tumors. Molecular Medicine. 2017; 15 (6): 38–45. DOI: 2310.2174/1389200219666180328113801. PMID: 29595102 (in Russian)]

补充文件

附件文件
动作
1. JATS XML
2. Fig. 1. Histogram of SSTR2, SSTR5, and DR2 expression (in points) in different groups

下载 (104KB)
3. Fig. 2. Immunohistochemical study with antibody to DR2 (brown staining) in zero-cell adenoma of patient G., 47 years old – expression was estimated at 3 points out of 4 (а); in prolactinoma of patient K., 30 years old – expression was estimated at 4 points out of 4 (б); in adenohypophysis without pathology of patient A., 68 years old – expression was estimated at 3 points out of 4 (в); in corticotropinoma of patient Ch., 42 years old – expression was estimated at 3 points out of 4 (г); ×200

下载 (770KB)
4. Fig. 3. Immunohistochemical study with an antibody to SSTR2 (brown staining) in the corticotropinoma of patient K., 54 years old – expression was estimated at 3 points out of 4 (а); in the normal adenohypophysis of patient C., 58 years old – expression was estimated at 2 points out of 4 (б); in the zero-cell adenoma of patient G., 57 years old – expression is absent (в); in the prolactinoma of patient D., 61 years old – expression is absent (г); ×200

下载 (583KB)
5. Fig. 4. Immunohistochemical study with antibody to SSTR5 in corticotropinoma of patient L., 43 years old – expression was estimated at 3 points out of 4 (а); in normal adenohypophysis of patient A., 56 years old – expression was estimated at 3 points out of 4 (б); in zero-cell adenoma of patient A. – expression was estimated at 4 points out of 4 (в); in prolactinoma of patient K., 43 years old – expression was estimated at 4 points out of 4 (г); ×200

下载 (667KB)
6. Fig. 5. Medians of DR2 expression in groups with prolactinomas and adenohypophysis without documented pathology. Abscissa axis: Group 1 – group with prolactinomas; Group 2 – group with normal adenohypophysis. Ordinate axis: DR2 expression severity in points

下载 (33KB)
7. Fig. 6. Graph of SSTR2 and DR2 expression in the group with prolactinomas. Abscissa axis – cases studied, ordinate axis – expression severity of markers in points: 1 – expression in single cells; 2 – focal expression; 3 – no expression in single cells; 4 – diffuse expression in all cells

下载 (75KB)
8. Fig. 7. Graph of SSTR5 and DR2 expression in the group with prolactinomas. Abscissa axis – cases studied, ordinate axis – expression severity of markers in points: 1 – expression in single cells; 2 – focal expression; 3 – no expression in single cells; 4 – diffuse expression in all cells

下载 (72KB)

版权所有 © Russkiy Vrach Publishing House, 2025