Evidence map›Paper›PMID 41258226›Full record

ArticleScientific reports2025

Immunohistochemical analysis of filamin a expression in acromegaly and its correlation with tumor characteristics and treatment response.

Maximilian Cosma Gliga, Laura Chinezu, Cristina Preda, Daniel Ilie Rotariu, Maria Ionela Pascanu

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Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Maximilian Cosma GligaEndocrinology Department, George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Târgu Mureș, Târgu Mureș, Romania.ORCID http://orcid.org/0000-0003-0032-194X
Laura ChinezuHistology Department, George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Târgu Mureș, Târgu Mureș, Romania. laura.chinezu@umfst.ro.ORCID http://orcid.org/0000-0003-3013-490X
Cristina PredaEndocrinology Department, Grigore T. Popa University of Medicine and Pharmacy Iasi, Iași, Romania.
Daniel Ilie RotariuNeurosurgery Department, Grigore T. Popa University of Medicine and Pharmacy Iasi, Iași, Romania.
Maria Ionela PascanuEndocrinology Department, George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Târgu Mureș, Târgu Mureș, Romania.ORCID http://orcid.org/0000-0003-0679-1379

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acromegaly, caused by growth hormone-secreting pituitary tumors, often causes significant challenges in its management due to poor surgical outcomes and resistance to pharmacological treatment. The present study aims to explore the expression of Filamin A (FLNA), a cytoskeletal protein involved in somatostatin receptor signaling, and its clinical relevance in acromegaly. We conducted immunohistochemical (IHC) study on 34 GH-secreting pituitary tumors to evaluate FLNA expression intensity and its associations with somatostatin receptors (SSTR2, SSTR5), E-Cadherin, tumor characteristics obtained through imaging studies, and pharmacological treatment responses. Our findings revealed a 100% FLNA positivity rate, with moderate to strong FLNA expression correlating significantly with SSTR5 expression and the presence of suprasellar tumor extension, indicating a potential role in tumor invasiveness. Moreover, patients with macrodenomas presented significantly higher FLNA intensity compared to the ones with microadenomas. FLNA expression showed no significant association with SSTR2, E-Cadherin, surgical cure rate or first-generation somatostatin receptor ligand (fgSRL) responses. However, the series of patients treated with Pasireotide (n = 4) demonstrated a trend suggesting better biochemical control with higher FLNA expression. In conclusion, our results suggest that FLNA may be associated with tumor invasiveness in GH-secreting pituitary tumors. While data on Pasireotide-treated patients are exploratory, further studies are needed to assess FLNA’s potential as a treatment response marker in acromegaly.

Indexed as

AcromegalyFilaminsGrowth Hormone-Secreting Pituitary AdenomaPituitary NeoplasmsAdenomaAdultAgedFemaleHumansImmunohistochemistryMaleMiddle AgedReceptors, SomatostatinTreatment OutcomeFilaminsFLNA protein, humanReceptors, Somatostatinsomatostatin receptor 5AcromegalyCytoskeletonFilamin AImmunohistochemistryPituitary

Identifiers

PMID41258226
PMCPMC12630665

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