Immunohistochemical somatostatin receptor expression in insulinomas |
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Author: | Peltola, Elina1,2; Vesterinen, Tiina3,4; Leijon, Helena3; |
Organizations: |
1Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland 2Department of Internal Medicine, Tampere University Hospital, Tampere, Finland 3HUS Diagnostic Center, HUSLAB, Department of Pathology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland
4Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Helsinki, Finland
5Endocrinology, Department of Internal Medicine, Tampere University Hospital, Tampere, Finland 6Faculty of Social Sciences, Tampere University, Tampere, Finland 7Research Unit of Cancer and Translational Medicine, Department of Pathology, University of Oulu and Department of Pathology, Oulu University Hospital, Oulu, Finland 8Fimlab Laboratories, Pathology Department, Tampere University Hospital, Tampere, Finland 9Department of Clinical Pathology, Kuopio University Hospital, Kuopio, Finland 10Department of Pathology, Turku University Hospital, Turku, Finland 11Division of Internal Medicine, Seinäjoki Central Hospital, Seinäjoki, Finland |
Format: | article |
Version: | accepted version |
Access: | embargoed |
Persistent link: | http://urn.fi/urn:nbn:fi-fe2023042739116 |
Language: | English |
Published: |
John Wiley & Sons,
2023
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Publish Date: | 2024-03-10 |
Description: |
AbstractInsulinomas 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. see all
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Series: |
APMIS |
ISSN: | 0903-4641 |
ISSN-E: | 1600-0463 |
ISSN-L: | 0903-4641 |
Volume: | 131 |
Issue: | 4 |
Pages: | 152 - 160 |
DOI: | 10.1111/apm.13297 |
OADOI: | https://oadoi.org/10.1111/apm.13297 |
Type of Publication: |
A1 Journal article – refereed |
Field of Science: |
3121 General medicine, internal medicine and other clinical medicine 3122 Cancers |
Subjects: | |
Funding: |
This work was supported by the Emil Aaltonen Foundation, the Finnish Cancer Foundation, the Helsinki University Hospital Research Fund, the Liv och Hälsa Foundation, the Medical Research Fund of Seinäjoki Central Hospital, and the Research Funding provided by Seinäjoki City, Tampere University and Tampere University Hospital. |
Copyright information: |
© 2023 Scandinavian Societies for Pathology, Medical Microbiology and Immunology. This is the peer reviewed version of the following article: Peltola, E., Vesterinen, T., Leijon, H., Hannula, P., Huhtala, H., Mäkinen, M., Nieminen, L., Pirinen, E., Rönty, M., Söderström, M., Arola, J. and Jaatinen, P. (2023), Immunohistochemical somatostatin receptor expression in insulinomas. APMIS, 131: 152-160, which has been published in final form at https://doi.org/10.1111/apm.13297. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited. |