Evidence map›Paper›PMID 29507229›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Myeloid ERK5 deficiency suppresses tumor growth by blocking protumor macrophage polarization via STAT3 inhibition.

Emanuele Giurisato, Qiuping Xu, Silvia Lonardi, Brian Telfer, Ilaria Russo, Adam Pearson, Katherine G Finegan, Wenbin Wang, Jinhua Wang, Nathanael S Gray and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
4.3field-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

65 citing papers in PubMed, 96 citations in OpenAlex.

  1. Review
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  3. Review
  4. Cellular signaling meets bacterial infection: the integrative role of STAT3.Frontiers in cellular and infection microbiology · 2026
    Review
  5. Review
  6. Efferocytosis: The Silent Guardian of Tissue Homeostasis and Cardiovascular Health.Journal of cardiovascular development and disease · 2025
    Review
  7. Review
  8. Article
  9. Review
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  12. Article
  13. Review
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  15. Article
  16. Review
  17. Macrophage Repolarization as a Therapeutic Strategy for Osteosarcoma.International journal of molecular sciences · 2023
    Review
  18. Article
  19. Review
  20. Review

5 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

13 authors at 7 institutions in 3 countries.

Emanuele GiurisatoDepartment of Molecular and Developmental Medicine, University of Siena, 53100 Siena, Italy; emanuele.giurisato@manchester.ac.uk cathy.tournier@manchester.ac.uk.ORCID 0000-0003-0598-6449
Qiuping XuDivision of Cancer Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom.
Silvia LonardiDepartment of Molecular and Translational Medicine, School of Medicine, University of Brescia, 25121 Brescia, Italy.
Brian TelferDivision of Pharmacy and Optometry, School of Health Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom.
Ilaria RussoDivision of Infection, Immunity and Respiratory Medicine, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom.
Adam PearsonDivision of Cancer Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom.
Katherine G FineganDivision of Pharmacy and Optometry, School of Health Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom.
Wenbin WangToxicology Program, Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98195.
Jinhua WangDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02115.
Nathanael S GrayDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02115.
William VermiDepartment of Molecular and Translational Medicine, School of Medicine, University of Brescia, 25121 Brescia, Italy.
Zhengui XiaToxicology Program, Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98195.
Cathy TournierDivision of Cancer Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom; emanuele.giurisato@manchester.ac.uk cathy.tournier@manchester.ac.uk.ORCID 0000-0002-4618-2570
University of Manchester · GBHarvard University · USManchester Academic Health Science Centre · GBUniversity of Washington · USUniversity of Brescia · ITUniversity of Siena · ITWashington University in St. Louis · US

Funding

Cancer Research UKWorldwide Cancer Research 15-1283
6 · The paper itself

Abstract

Owing to the prevalence of tumor-associated macrophages (TAMs) in cancer and their unique influence upon disease progression and malignancy, macrophage-targeted interventions have attracted notable attention in cancer immunotherapy. However, tractable targets to reduce TAM activities remain very few and far between because the signaling mechanisms underpinning protumor macrophage phenotypes are largely unknown. Here, we have investigated the role of the extracellular-regulated protein kinase 5 (ERK5) as a determinant of macrophage polarity. We report that the growth of carcinoma grafts was halted in myeloid ERK5-deficient mice. Coincidentally, targeting ERK5 in macrophages induced a transcriptional switch in favor of proinflammatory mediators. Further molecular analyses demonstrated that activation of the signal transducer and activator of transcription 3 (STAT3) via Tyr705 phosphorylation was impaired in

Indexed as

AnimalsAntigens, CDAntigens, Differentiation, MyelomonocyticCD163 AntigenCell PolarityHumansMacrophagesMice, Inbred C57BLMice, TransgenicMitogen-Activated Protein Kinase 7NeoplasmsPhosphorylationReceptors, Cell SurfaceSTAT3 Transcription FactorTyrosineXenograft Model Antitumor AssaysAntigens, CDAntigens, Differentiation, MyelomonocyticCD163 AntigenMitogen-Activated Protein Kinase 7Receptors, Cell SurfaceSTAT3 protein, humanStat3 protein, mouseSTAT3 Transcription FactorTyrosineERK5macrophagesMAPKSTAT3tumors

Identifiers

PMID29507229
PMCPMC5866536
OpenAlexW2788742274

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.