Evidence map›Paper›PMID 41751264›Full record

ReviewBiomedicines2026

Immunosuppressive Environment of Pancreatic NENs-A Review.

Jacek Kabut, Anita Gorzelak-Magiera, Jakub Sokołowski, Wiktoria Żelazna, Mateusz Stępień, Marta Strauchman, Natalia Jaworska, Beata Kos-Kudła, Iwona Gisterek-Grocholska

Abstract readReview
In one paragraph

Review in Biomedicines, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Jacek KabutDepartment of Oncology and Radiotherapy, Medical University of Silesia, 40-615 Katowice, Poland.ORCID 0000-0002-0873-4952
Anita Gorzelak-MagieraDepartment of Oncology and Radiotherapy, Medical University of Silesia, 40-615 Katowice, Poland.ORCID 0000-0003-4183-4522
Jakub SokołowskiStudent Scientific Club, Department and Clinic of Oncology and Radiotherapy, The Faculty of Medical Sciences, Medical University of Silesia, 40-615 Katowice, Poland.ORCID 0009-0008-7031-5311
Wiktoria ŻelaznaStudent Scientific Club, Department and Clinic of Oncology and Radiotherapy, The Faculty of Medical Sciences, Medical University of Silesia, 40-615 Katowice, Poland.ORCID 0009-0001-8185-4846
Mateusz StępieńStudent Scientific Club, Department and Clinic of Oncology and Radiotherapy, The Faculty of Medical Sciences, Medical University of Silesia, 40-615 Katowice, Poland.ORCID 0009-0000-7313-0437
Marta StrauchmanStudent Scientific Club, Department and Clinic of Oncology and Radiotherapy, The Faculty of Medical Sciences, Medical University of Silesia, 40-615 Katowice, Poland.
Natalia JaworskaStudent Scientific Club, Department and Clinic of Oncology and Radiotherapy, The Faculty of Medical Sciences, Medical University of Silesia, 40-615 Katowice, Poland.
Beata Kos-KudłaDepartment of Endocrinology and Neuroendocrine Tumours, Department of Pathophysiology and Endocrinology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, Katowice, ul. Ceglana 35, 40-514 Katowice, Poland.ORCID 0000-0003-3755-1722
Iwona Gisterek-GrocholskaDepartment of Oncology and Radiotherapy, Medical University of Silesia, 40-615 Katowice, Poland.ORCID 0000-0002-6320-0224

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic neuroendocrine neoplasms (pNENs) are rare tumors with significant biological diversity. Despite significant improvements in diagnostics and a growing range of available therapies, long-term disease control remains difficult in advanced cases. The tumor microenvironment, which in pNENs adopts a predominantly immunosuppressive profile and promotes tumor development, is attracting increasing attention. A complex network of interactions dominates the tumor tissue, including M2 macrophages, regulatory T cells, and numerous pathways that inhibit effector lymphocyte activity. M2 macrophages, through the secretion of anti-inflammatory cytokines and exosome-mediated signaling, support angiogenesis while simultaneously attenuating the cytotoxic response. Simultaneously, receptors and ligands associated with immune checkpoints are overexpressed. In addition to classic molecules such as PD-1/PD-L1 and CTLA-4, the role of B7x and CD276 is increasingly being emphasized, as their presence correlates with rapid disease progression and poor prognosis. To date, attempts to use checkpoint inhibitors as monotherapy have yielded modest clinical benefits. However, approaches based on combination strategies-both in the form of dual immune blockade and in combination with chemotherapy or angiogenesis-targeted therapy-have shown significantly greater activity. Therapies using tyrosine kinase inhibitors, such as sunitinib and newer drugs (lenvatinib, surufatinib, cabozantinib), may partially normalize the tumor's disrupted vascular architecture and thus increase its susceptibility to immunological interventions. In the coming years, it will be crucial not only to overcome the immunosuppressive nature of the TME but also to identify predictive biomarkers that will allow for more precise patient selection. This approach may open the way to more effective, personalized therapies for pNENs.

Indexed as

antiangiogenic therapyimmune checkpointsimmunosuppressionimmunotherapypancreatic neuroendocrine tumorstumor microenvironment

Identifiers

PMID41751264
PMCPMC12937858

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.