Evidence map›Paper›PMID 35122059›Full record

ArticleNature cancer2021

TNF-α-producing macrophages determine subtype identity and prognosis via AP1 enhancer reprogramming in pancreatic cancer.

Mengyu Tu, Lukas Klein, Elisa Espinet, Theodoros Georgomanolis, Florian Wegwitz, Xiaojuan Li, Laura Urbach, Adi Danieli-Mackay, Stefan Küffer, Kamil Bojarczuk and 13 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

79 citing papers in PubMed, 112 citations in OpenAlex.

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  5. Pancreatic cancer.Nature reviews. Disease primers · 2026
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19 more citing papers are in PubMed but not listed here.

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

23 authors at 6 institutions in 2 countries.

Mengyu Tu *Department of Gastroenterology, Gastrointestinal Oncology and Endocrinology, University Medical Center Göttingen, Göttingen, Germany.
Lukas Klein *Department of Gastroenterology, Gastrointestinal Oncology and Endocrinology, University Medical Center Göttingen, Göttingen, Germany.
Elisa EspinetDivision of Stem Cells and Cancer, DKFZ, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-0690-9878
Theodoros GeorgomanolisCologne Center for Genomics, University of Cologne, Cologne, Germany.
Florian WegwitzDepartment of Gynecology and Obstetrics, University Medical Center Göttingen, Göttingen, Germany.ORCID http://orcid.org/0000-0003-0750-6998
Xiaojuan LiDepartment of Developmental Biology, Göttingen Center for Molecular Biosciences, Göttingen, Germany.
Laura UrbachDepartment of Gastroenterology, Gastrointestinal Oncology and Endocrinology, University Medical Center Göttingen, Göttingen, Germany.
Adi Danieli-MackayInstitute of Pathology, University Medical Center Göttingen, Göttingen, Germany.
Stefan KüfferInstitute of Pathology, University Medical Center Göttingen, Göttingen, Germany.
Kamil BojarczukDepartment of Hematology and Medical Oncology, University Medical Center Göttingen, Göttingen, Germany.ORCID http://orcid.org/0000-0002-6110-4060
Athanasia MiziInstitute of Pathology, University Medical Center Göttingen, Göttingen, Germany.
Ufuk GünesdoganDepartment of Developmental Biology, Göttingen Center for Molecular Biosciences, Göttingen, Germany.
Björn ChapuyDepartment of Hematology and Medical Oncology, University Medical Center Göttingen, Göttingen, Germany.ORCID http://orcid.org/0000-0002-6485-8773
Zuguang GuBioinformatics and Omics Data Analytics, DKFZ, Heidelberg, Germany.
Albrecht NeesseDepartment of Gastroenterology, Gastrointestinal Oncology and Endocrinology, University Medical Center Göttingen, Göttingen, Germany.
Uday KishoreBiosciences, College of Health, Medicine and Life Sciences, Brunel University London, Uxbridge, UK.
Philipp StröbelInstitute of Pathology, University Medical Center Göttingen, Göttingen, Germany.
Elisabeth HessmannDepartment of Gastroenterology, Gastrointestinal Oncology and Endocrinology, University Medical Center Göttingen, Göttingen, Germany.
Stephan A HahnFaculty of Medicine, Department of Molecular GI Oncology, Ruhr University Bochum, Bochum, Germany.
Andreas TrumppDivision of Stem Cells and Cancer, DKFZ, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-6212-3466
Argyris PapantonisInstitute of Pathology, University Medical Center Göttingen, Göttingen, Germany.ORCID http://orcid.org/0000-0001-7551-1073
Volker EllenriederDepartment of Gastroenterology, Gastrointestinal Oncology and Endocrinology, University Medical Center Göttingen, Göttingen, Germany.
Shiv K SinghDepartment of Gastroenterology, Gastrointestinal Oncology and Endocrinology, University Medical Center Göttingen, Göttingen, Germany. shiv.singh@med.uni-goettingen.de.ORCID http://orcid.org/0000-0002-5725-4058
Universitätsmedizin Göttingen · DEHeidelberg University · DEUniversity of Göttingen · DEBrunel University of London · GBRuhr University Bochum · DEUniversity of Cologne · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Large-scale genomic profiling of pancreatic cancer (PDAC) has revealed two distinct subtypes: 'classical' and 'basal-like'. Their variable coexistence within the stromal immune microenvironment is linked to differential prognosis; however, the extent to which these neoplastic subtypes shape the stromal immune landscape and impact clinical outcome remains unclear. By combining preclinical models, patient-derived xenografts, as well as FACS-sorted PDAC patient biopsies, we show that the basal-like neoplastic state is sustained via BRD4-mediated cJUN/AP1 expression, which induces CCL2 to recruit tumor necrosis factor (TNF)-α-secreting macrophages. TNF-α

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsBromodomain Containing ProteinsCell Cycle ProteinsGene Expression Regulation, NeoplasticHumansMacrophagesNuclear ProteinsPrognosisTranscription FactorsTumor MicroenvironmentTumor Necrosis Factor-alphaBRD4 protein, humanBromodomain Containing ProteinsCell Cycle ProteinsNuclear ProteinsTranscription FactorsTumor Necrosis Factor-alpha

Identifiers

PMID35122059
OpenAlexW3214546142

What OpenQuestion holds

Textmetadata
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.