Evidence map›Paper›PMID 29038174›Full record

ArticleThe EMBO journal2017

Tumor-associated macrophages (TAMs) depend on ZEB1 for their cancer-promoting roles.

Marlies Cortés, Lidia Sanchez-Moral, Oriol de Barrios, María J Fernández-Aceñero, M C Martínez-Campanario, Anna Esteve-Codina, Douglas S Darling, Balázs Győrffy, Toby Lawrence, Douglas C Dean and 1 more

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

101 citing papers in PubMed, 200 citations in OpenAlex.

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41 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

11 authors at 8 institutions in 4 countries.

Marlies CortésGroup of Transcriptional Regulation of Gene Expression, Department of Oncology and Hematology, IDIBAPS, Barcelona, Spain.
Lidia Sanchez-MoralGroup of Transcriptional Regulation of Gene Expression, Department of Oncology and Hematology, IDIBAPS, Barcelona, Spain.
Oriol de BarriosGroup of Transcriptional Regulation of Gene Expression, Department of Oncology and Hematology, IDIBAPS, Barcelona, Spain.
María J Fernández-AceñeroDepartment of Pathology, Hospital Clínico San Carlos, Madrid, Spain.
M C Martínez-CampanarioGroup of Transcriptional Regulation of Gene Expression, Department of Oncology and Hematology, IDIBAPS, Barcelona, Spain.
Anna Esteve-CodinaCNAG-CRG, Centre for Genomic Regulation, Barcelona Institute of Science & Technology, and Universitat Pompeu Fabra, Barcelona, Spain.
Douglas S DarlingDepartment of Oral Immunology, and Center for Genetics and Molecular Medicine, University of Louisville, Louisville, KY, USA.
Balázs GyőrffyMTA TTK Lendület Cancer Biomarker Research Group, Institute of Enzymology, and Semmelweis University 2 Department of Pediatrics, Budapest, Hungary.
Toby LawrenceCentre d'Immunologie de Marseille-Luminy, INSERM U1104 and CNRS MR7280, Marseille, France.
Douglas C DeanDepartment of Ophthalmology and Visual Sciences and Birth Defects Center, University of Louisville, Louisville, KY, USA.
Antonio PostigoGroup of Transcriptional Regulation of Gene Expression, Department of Oncology and Hematology, IDIBAPS, Barcelona, Spain idib412@clinic.cat.ORCID 0000-0003-4605-2634
Consorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESCentre National de la Recherche Scientifique · FRHospital Clínico San Carlos · ESInstitució Catalana de Recerca i Estudis Avançats · ESSemmelweis University · HUTarget (United States) · USUniversitat Pompeu Fabra · ESUniversity of Louisville · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulation of tumor-associated macrophages (TAMs) associates with malignant progression in cancer. However, the mechanisms that drive the pro-tumor functions of TAMs are not fully understood. ZEB1 is best known for driving an epithelial-to-mesenchymal transition (EMT) in cancer cells to promote tumor progression. However, a role for ZEB1 in macrophages and TAMs has not been studied. Here we describe that TAMs require ZEB1 for their tumor-promoting and chemotherapy resistance functions in a mouse model of ovarian cancer. Only TAMs that expressed full levels of

Indexed as

AnimalsAntigens, Differentiation, B-LymphocyteCarcinogenesisCell CountCell DifferentiationChemokine CCL2Colony-Stimulating FactorsDisease Models, AnimalDisease ProgressionDrug Resistance, NeoplasmFemaleGene Expression Regulation, NeoplasticHistocompatibility Antigens Class IIHumansMacrophage ActivationMacrophagesAntigens, Differentiation, B-LymphocyteCcr2 protein, mouseChemokine CCL2Colony-Stimulating FactorsHistocompatibility Antigens Class IIinvariant chainMatrix Metalloproteinase 9Receptors, CCR2ZEB1 protein, humanZEB1 protein, mouseZinc Finger E-box-Binding Homeobox 1EMTmacrophagesTAMstumor microenvironmentZEB1

Identifiers

PMID29038174
PMCPMC5686549
OpenAlexW2767071425

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.