Immunohistochemical somatostatin receptor expression in insulinomas

dc.contributor.authorPeltola Elina
dc.contributor.authorVesterinen Tiina
dc.contributor.authorLeijon Helena
dc.contributor.authorHannula Päivi
dc.contributor.authorHuhtala Heini
dc.contributor.authorMäkinen Markus
dc.contributor.authorNieminen Lasse
dc.contributor.authorPirinen Elina
dc.contributor.authorRönty Mikko
dc.contributor.authorSöderström Mirva
dc.contributor.authorArola Johanna
dc.contributor.authorJaatinen Pia
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code2607100
dc.converis.publication-id178886485
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/178886485
dc.date.accessioned2025-08-28T00:39:50Z
dc.date.available2025-08-28T00:39:50Z
dc.description.abstract<p>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.<br></p>
dc.format.pagerange152
dc.format.pagerange160
dc.identifier.jour-issn0903-4641
dc.identifier.olddbid206153
dc.identifier.oldhandle10024/189180
dc.identifier.urihttps://www.utupub.fi/handle/11111/43219
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1111/apm.13297
dc.identifier.urnURN:NBN:fi-fe2025082791161
dc.language.isoen
dc.okm.affiliatedauthorSöderström, Mirvamaaria
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3122 Cancersen_GB
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.discipline3122 Syöpätauditfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherJohn Wiley and Sons Inc
dc.publisher.countryDenmarken_GB
dc.publisher.countryTanskafi_FI
dc.publisher.country-codeDK
dc.relation.doi10.1111/apm.13297
dc.relation.ispartofjournalAPMIS
dc.relation.issue4
dc.relation.volume131
dc.source.identifierhttps://www.utupub.fi/handle/10024/189180
dc.titleImmunohistochemical somatostatin receptor expression in insulinomas
dc.year.issued2023

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