Evidence map›Paper›PMID 39178229›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Platelet-activating factor (PAF) promotes immunosuppressive neutrophil differentiation within tumors.

Ankit Dahal, Yeonsun Hong, Jocelyn S Mathew, Adam Geber, Sarah Eckl, Stephanie Renner, Cooper J Sailer, Allison T Ryan, Sana Mir, Kihong Lim and 3 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Platelet-activating factor (PAF) promotes immunosuppressive neutrophil differentiation within tumors.Proceedings of the National Academy of Sciences of the United States of America · 2024
    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

13 authors.

Ankit DahalDepartment of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY.ORCID 0009-0005-6792-8203
Yeonsun HongDepartment of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY.
Jocelyn S MathewDepartment of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY.
Adam GeberDepartment of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY.
Sarah EcklDepartment of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY.ORCID 0000-0002-4577-2480
Stephanie RennerDepartment of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY.
Cooper J SailerDepartment of Pathology, University of Rochester Medical Center, Rochester, NY.ORCID 0000-0001-8055-588X
Allison T RyanDepartment of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY.ORCID 0000-0002-5133-8373
Sana MirDepartment of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY.ORCID 0009-0002-2073-1276
Kihong LimDepartment of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY.ORCID 0000-0001-6665-6422
David C LinehanDepartment of Surgery, University of Rochester Medical Center, Rochester, NY.
Scott A GerberDepartment of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY.
Minsoo KimDepartment of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY.ORCID 0000-0002-9566-9385

Funding

Tissue regulation of T cell function - Reagents CoreP01AI102851 · NIAID · UNIVERSITY OF ROCHESTER · PI Iwijn De Vlaminck · 2014 to 2026
$26.0M
University of Rochester Mentoring Environment: Nurturing Training Opportunities in Research (UR-MENTOR)T32GM007356 · NIGMS · UNIVERSITY OF ROCHESTER · PI O'BANION, M. KERRY · 1985 to 2023
$15.1M
T cell migration and cardiovascular toxicity in immunotherapyR01AI147362 · NIAID · UNIVERSITY OF ROCHESTER · PI Minsoo Kim, Richard E Waugh · 2019 to 2026
$4.2M
Complement C1q and sepsis associated fatalitiesR01HL160723 · NHLBI · UNIVERSITY OF ROCHESTER · PI KIM, MINSOO, PIETROPAOLI, ANTHONY P · 2022 to 2025
$2.7M
HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) HL160723HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) Al102851HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) Al147362HHS | NIH | National Institute of General Medical Sciences (NIGMS) GM007356NHLBI NIH HHS R01 HL160723NIGMS NIH HHS T32 GM007356
6 · The paper itself

Abstract

Chronic inflammatory milieu in the tumor microenvironment (TME) leads to the recruitment and differentiation of myeloid-derived suppressor cells (MDSCs). Polymorphonuclear (PMN)-MDSCs, which are phenotypically and morphologically defined as a subset of neutrophils, cause major immune suppression in the TME, posing a significant challenge in the development of effective immunotherapies. Despite recent advances in our understanding of PMN-MDSC functions, the mechanism that gives rise to immunosuppressive neutrophils within the TME remains elusive. Both in vivo and in vitro, newly recruited neutrophils into the tumor sites remained activated and highly motile for several days and developed immunosuppressive phenotypes, as indicated by increased arginase 1 (Arg1) and dcTrail-R1 expression and suppressed anticancer CD8 T cell cytotoxicity. The strong suppressive function was successfully recapitulated by incubating naive neutrophils with cancer cell culture supernatant in vitro. Cancer metabolite secretome analyses of the culture supernatant revealed that both murine and human cancers released lipid mediators to induce the differentiation of immunosuppressive neutrophils. Liquid chromatography-mass spectrometry (LC-MS) lipidomic analysis identified platelet-activation factor (PAF; 1-

Indexed as

Cell DifferentiationMyeloid-Derived Suppressor CellsNeutrophilsPlatelet Activating FactorTumor MicroenvironmentAnimalsCD8-Positive T-LymphocytesCell Line, TumorHumansMiceMice, Inbred C57BLPlatelet Activating FactorCancerMDSCmyeloid cellsneutrophiltumor microenvironment

Identifiers

PMID39178229
PMCPMC11363292

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.