Evidence map›Paper›PMID 36417691›Full record

ArticleAdvanced healthcare materials2023

A Tumor Microenvironment Model of Pancreatic Cancer to Elucidate Responses toward Immunotherapy.

Verena Kast, Ali Nadernezhad, Dagmar Pette, Anastasiia Gabrielyan, Maximilian Fusenig, Kim C Honselmann, Daniel E Stange, Carsten Werner, Daniela Loessner

Open access · hybridAbstract read
In one paragraph

Article in Advanced healthcare materials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.5field-weighted citation impact, top 8% of its field
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

13 citing papers in PubMed, 24 citations in OpenAlex.

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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 at 3 institutions in 2 countries.

Verena KastLeibniz Institute of Polymer Research Dresden e.V, Max Bergmann Centre of Biomaterials, Hohe Straße 6, 01069, Dresden, Germany.
Ali NadernezhadLeibniz Institute of Polymer Research Dresden e.V, Max Bergmann Centre of Biomaterials, Hohe Straße 6, 01069, Dresden, Germany.
Dagmar PetteLeibniz Institute of Polymer Research Dresden e.V, Max Bergmann Centre of Biomaterials, Hohe Straße 6, 01069, Dresden, Germany.
Anastasiia GabrielyanLeibniz Institute of Polymer Research Dresden e.V, Max Bergmann Centre of Biomaterials, Hohe Straße 6, 01069, Dresden, Germany.
Maximilian FusenigLeibniz Institute of Polymer Research Dresden e.V, Max Bergmann Centre of Biomaterials, Hohe Straße 6, 01069, Dresden, Germany.
Kim C HonselmannDepartment of Surgery, University Medical Center Schleswig-Holstein, Campus Lübeck, 23562, Lübeck, Germany.
Daniel E StangeDepartment of Visceral, Thoracic and Vascular Surgery, University Hospital Carl Gustav Carus, Medical Faculty, Technical University Dresden, 01307, Dresden, Germany.
Carsten WernerLeibniz Institute of Polymer Research Dresden e.V, Max Bergmann Centre of Biomaterials, Hohe Straße 6, 01069, Dresden, Germany.
Daniela LoessnerLeibniz Institute of Polymer Research Dresden e.V, Max Bergmann Centre of Biomaterials, Hohe Straße 6, 01069, Dresden, Germany.ORCID 0000-0001-5891-3441
Leibniz Institute of Polymer Research · DEUniversity Hospital Carl Gustav Carus · DEUniversity of Lübeck · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer is a devastating malignancy with minimal treatment options. Standard-of-care therapy, including surgery and chemotherapy, is unsatisfactory, and therapies harnessing the immune system have been unsuccessful in clinical trials. Resistance to therapy and disease progression are mediated by the tumor microenvironment, which contains excessive amounts of extracellular matrix and stromal cells, acting as a barrier to drug delivery. There is a lack of preclinical pancreatic cancer models that reconstruct the extracellular, cellular, and biomechanical elements of tumor tissues to assess responses toward immunotherapy. To address this limitation and explore the effects of immunotherapy in combination with chemotherapy, a multicellular 3D cancer model using a star-shaped poly(ethylene glycol)-heparin hydrogel matrix is developed. Human pancreatic cancer cells, cancer-associated fibroblasts, and myeloid cells are grown encapsulated in hydrogels to mimic key components of tumor tissues, and cell responses toward treatment are assessed. Combining the CD11b agonist ADH-503 with anti-PD-1 immunotherapy and chemotherapy leads to a significant reduction in tumor cell viability, proliferation, metabolic activity, immunomodulation, and secretion of immunosuppressive and tumor growth-promoting cytokines.

Indexed as

Pancreatic NeoplasmsTumor MicroenvironmentHumansImmunomodulationImmunotherapy3D cancer modelsCD11b agonistextracellular matrixhydrogelsimmunotherapy

Identifiers

PMID36417691
PMCPMC11468239
OpenAlexW4309859183

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.