Immunohistochemical somatostatin receptor expression in insulinomas

Author:

Peltola Elina12ORCID,Vesterinen Tiina34ORCID,Leijon Helena3ORCID,Hannula Päivi15ORCID,Huhtala Heini6ORCID,Mäkinen Markus7ORCID,Nieminen Lasse8,Pirinen Elina9,Rönty Mikko3,Söderström Mirva10,Arola Johanna3ORCID,Jaatinen Pia1211ORCID

Affiliation:

1. Faculty of Medicine and Health Technology Tampere University Tampere Finland

2. Department of Internal Medicine Tampere University Hospital Tampere Finland

3. HUS Diagnostic Center, HUSLAB, Department of Pathology University of Helsinki and Helsinki University Hospital Helsinki Finland

4. Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki Helsinki Finland

5. Endocrinology, Department of Internal Medicine Tampere University Hospital Tampere Finland

6. Faculty of Social Sciences Tampere University Tampere Finland

7. Research Unit of Cancer and Translational Medicine, Department of Pathology University of Oulu and Department of Pathology, Oulu University Hospital Oulu Finland

8. Fimlab Laboratories, Pathology Department Tampere University Hospital Tampere Finland

9. Department of Clinical Pathology Kuopio University Hospital Kuopio Finland

10. Department of Pathology Turku University Hospital Turku Finland

11. Division of Internal Medicine Seinäjoki Central Hospital Seinäjoki Finland

Abstract

Insulinomas are rare pancreatic neuroendocrine tumours. Most patients can be cured with surgery, but patients with a metastatic disease show impaired survival. The aim of this study was to evaluate somatostatin receptor (SSTR) 1‐5 expression in insulinomas and to correlate the expression profile with clinicopathological variables and with patient outcome. This retrospective study involved 52 insulinoma patients. After histological re‐evaluation, formalin‐fixed paraffin‐embedded tissue samples were processed into tissue microarrays and stained immunohistochemically with monoclonal SSTR1‐5 antibodies. All the 52 tumours (49 non‐metastatic, 3 metastatic) expressed at least one SSTR subtype. SSTR2 was expressed most frequently (71%), followed by SSTR3 (33%), SSTR1 (27%), SSTR5 (6%) and SSTR4 (0%). SSTR3 expression was associated with a larger tumour size (median diameter 19 mm vs. 13 mm, p = 0.043), and SSTR3 and SSTR5 expression were associated with impaired overall survival [HR 3.532 (95% CI 1.106–11,277), p = 0.033, and HR 6.805 (95% CI 1.364–33.955), p = 0.019 respectively]. Most insulinomas express SSTR2, which may be utilized in diagnostic imaging, and in planning individualized treatment strategies for insulinoma patients. Further studies are needed to clarify the association between SSTR profile and overall survival.

Funder

Emil Aaltosen Säätiö

Tays

Publisher

Wiley

Subject

Microbiology (medical),General Medicine,Immunology and Allergy,Pathology and Forensic Medicine

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