Evidence map›Paper›PMID 34903606›Full record

ArticleCancer research2022

HDAC2 Facilitates Pancreatic Cancer Metastasis.

Lukas Krauß, Bettina C Urban, Sieglinde Hastreiter, Carolin Schneider, Patrick Wenzel, Zonera Hassan, Matthias Wirth, Katharina Lankes, Andrea Terrasi, Christine Klement and 12 more

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Integrative single-cell analysis revealsFrontiers in immunology · 2026
    Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. FAP-targeted radioligand therapy withJournal for immunotherapy of cancer · 2025
    Article
  13. Article
  14. A Novel AMPK Inhibitor Sensitizes Pancreatic Cancer Cells to Ferroptosis Induction.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
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

22 authors at 8 institutions in 1 country.

Lukas Krauß *Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University Munich, München, Germany.ORCID 0000-0003-0062-8685
Bettina C Urban *Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University Munich, München, Germany.
Sieglinde Hastreiter *Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University Munich, München, Germany.
Carolin Schneider *Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University Munich, München, Germany.
Patrick WenzelMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University Munich, München, Germany.
Zonera HassanMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University Munich, München, Germany.
Matthias WirthDepartment of Hematology, Oncology and Tumor Immunology, Campus Benjamin Franklin, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, German.ORCID 0000-0002-8340-0872
Katharina LankesMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University Munich, München, Germany.
Andrea TerrasiDivision of Molecular Biology, Biomedical Center, Faculty of Medicine, LMU Munich, Planegg-Martinsried, Germany.
Christine KlementDivision of Molecular Biology, Biomedical Center, Faculty of Medicine, LMU Munich, Planegg-Martinsried, Germany.ORCID 0000-0003-1446-3703
Filippo M CernilogarDivision of Molecular Biology, Biomedical Center, Faculty of Medicine, LMU Munich, Planegg-Martinsried, Germany.ORCID 0000-0003-2814-3436
Rupert ÖllingerInstitute of Molecular Oncology and Functional Genomics, Technical University Munich, München, Germany.ORCID 0000-0002-2292-5982
Niklas de Andrade KrätzigInstitute of Molecular Oncology and Functional Genomics, Technical University Munich, München, Germany.ORCID 0000-0003-2141-6745
Thomas EngleitnerInstitute of Molecular Oncology and Functional Genomics, Technical University Munich, München, Germany.
Roland M SchmidMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University Munich, München, Germany.
Katja SteigerInstitute of Pathology, Technische Universität München, München, Germany.ORCID 0000-0002-7269-5433
Roland RadInstitute of Molecular Oncology and Functional Genomics, Technical University Munich, München, Germany.
Oliver H KrämerDepartment of Toxicology, University of Mainz Medical Center, Mainz, Germany.ORCID 0000-0003-3973-045X
Maximilian ReichertMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University Munich, München, Germany.
Gunnar SchottaDivision of Molecular Biology, Biomedical Center, Faculty of Medicine, LMU Munich, Planegg-Martinsried, Germany.ORCID 0000-0003-4940-6135
Dieter SaurGerman Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK), Heidelberg, Germany.ORCID 0000-0001-5874-0210
Günter SchneiderMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University Munich, München, Germany.
TUM Klinikum · DEGerman Cancer Research Center · DETechnical University of Munich · DEUrologische Klinik München · DECenter for Integrated Protein Science Munich · DEHumboldt-Universität zu Berlin · DEJohannes Gutenberg University Mainz · DEMunich University of Applied Sciences · DE

Funding

Deutsche Krebshilfe 70113760DFG SFB1321Wilhelm-Sander-Stiftung 2017.048.2
6 · The paper itself

Abstract

The mortality of patients with pancreatic ductal adenocarcinoma (PDAC) is strongly associated with metastasis, a multistep process that is incompletely understood in this disease. Although genetic drivers of PDAC metastasis have not been defined, transcriptional and epigenetic rewiring can contribute to the metastatic process. The epigenetic eraser histone deacetylase 2 (HDAC2) has been connected to less differentiated PDAC, but the function of HDAC2 in PDAC has not been comprehensively evaluated. Using genetically defined models, we show that HDAC2 is a cellular fitness factor that controls cell cycle in vitro and metastasis in vivo, particularly in undifferentiated, mesenchymal PDAC cells. Unbiased expression profiling detected a core set of HDAC2-regulated genes. HDAC2 controlled expression of several prosurvival receptor tyrosine kinases connected to mesenchymal PDAC, including PDGFRα, PDGFRβ, and EGFR. The HDAC2-maintained program disabled the tumor-suppressive arm of the TGFβ pathway, explaining impaired metastasis formation of HDAC2-deficient PDAC. These data identify HDAC2 as a tractable player in the PDAC metastatic cascade. The complexity of the function of epigenetic regulators like HDAC2 implicates that an increased understanding of these proteins is needed for implementation of effective epigenetic therapies. SIGNIFICANCE: HDAC2 has a context-specific role in undifferentiated PDAC and the capacity to disseminate systemically, implicating HDAC2 as targetable protein to prevent metastasis.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCarcinoma, Pancreatic DuctalCell CycleCell Line, TumorCell ProliferationEpithelial-Mesenchymal TransitionGene Expression ProfilingHistone Deacetylase 2HumansKaplan-Meier EstimateMiceMice, 129 StrainMice, Inbred C57BLMice, KnockoutNeoplasm MetastasisHistone Deacetylase 2

Identifiers

PMID34903606
PMCPMC9359718
OpenAlexW4200065240

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.