Evidence map›Paper›PMID 35119792›Full record

ArticleEMBO molecular medicine2022

Identification of treatment-induced vulnerabilities in pancreatic cancer patients using functional model systems.

Katja Peschke, Hannah Jakubowsky, Arlett Schäfer, Carlo Maurer, Sebastian Lange, Felix Orben, Raquel Bernad, Felix N Harder, Matthias Eiber, Rupert Öllinger and 15 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 6% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Advanced Human Immune Cell-Organoid Co-Cultures for Functional Testing of Cancer Nanovaccines.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  6. Observational
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  17. Article
  18. In-vitro model to mimic T cell subset change in human PDAC organoid co-culture.Journal of cancer research and clinical oncology · 2023
    Article
  19. Review
  20. Article
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

25 authors at 4 institutions in 1 country.

Katja Peschke *Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany.
Hannah Jakubowsky *Institute for Translational Cancer Research and Experimental Cancer Therapy, Technical University of Munich, Munich, Germany.
Arlett SchäferMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany.
Carlo MaurerMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany.ORCID 0000-0002-2193-6014
Sebastian LangeMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany.ORCID 0000-0003-0406-1401
Felix OrbenMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany.ORCID 0000-0002-2196-8702
Raquel BernadMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany.
Felix N HarderInstitute of Diagnostic and Interventional Radiology, Technical University of Munich, Munich, Germany.
Matthias EiberDepartment of Nuclear Medicine, Klinikum Rechts der Isar, Technical University of Munich, Munich, Germany.
Rupert ÖllingerInstitute of Molecular Oncology and Functional Genomics, TUM School of Medicine, Technical University of Munich, Munich, Germany.ORCID 0000-0002-2292-5982
Katja SteigerInstitute of Pathology, Technical University of Munich, München, Germany.
Melissa SchlitterInstitute of Pathology, Technical University of Munich, München, Germany.
Wilko WeichertInstitute of Pathology, Technical University of Munich, München, Germany.
Ulrich MayrMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany.
Veit PhillipMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany.
Christoph SchlagMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany.
Roland M SchmidMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany.
Rickmer F BrarenInstitute of Diagnostic and Interventional Radiology, Technical University of Munich, Munich, Germany.
Bo KongDepartment of Surgery, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Ihsan Ekin DemirDepartment of Surgery, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Helmut FriessDepartment of Surgery, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Roland RadInstitute of Molecular Oncology and Functional Genomics, TUM School of Medicine, Technical University of Munich, Munich, Germany.
Dieter SaurInstitute for Translational Cancer Research and Experimental Cancer Therapy, Technical University of Munich, Munich, Germany.ORCID 0000-0001-5874-0210
Günter Schneider *Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany.ORCID 0000-0003-1840-4508
Maximilian Reichert *Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany.ORCID 0000-0002-8611-5639
TUM Klinikum · DEGerman Cancer Research Center · DETechnical University of Munich · DEUniversität Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the advance and success of precision oncology in gastrointestinal cancers, the frequency of molecular-informed therapy decisions in pancreatic ductal adenocarcinoma (PDAC) is currently neglectable. We present a longitudinal precision oncology platform based on functional model systems, including patient-derived organoids, to identify chemotherapy-induced vulnerabilities. We demonstrate that treatment-induced tumor cell plasticity in vivo distinctly changes responsiveness to targeted therapies, without the presence of a selectable genetic marker, indicating that tumor cell plasticity can be functionalized. By adding a mechanistic layer to precision oncology, adaptive processes of tumors under therapy can be exploited, particularly in highly plastic tumors, such as pancreatic cancer.

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsHumansOrganoidsPrecision Medicinefunctional screeningpancreatic cancerprecision oncologytherapy-induced vulnerabilitiestumor cell plasticity

Identifiers

PMID35119792
PMCPMC8988213
OpenAlexW4210344402

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.