Evidence map›Paper›PMID 32452014›Full record

ArticleInternational journal of cancer2020

Blockade of p38 kinase impedes the mobilization of protumorigenic myeloid populations to impact breast cancer metastasis.

Justin Zonneville, Sean Colligan, Sydney Grant, Alexandra Miller, Paul Wallace, Scott I Abrams, Andrei V Bakin

Open access · hybridAbstract read
In one paragraph

Article in International journal of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

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  7. Gamma synuclein promotes cancer metastasis through the MKK3/6-p38MAPK cascade.International journal of biological sciences · 2022
    Article
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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

7 authors at 2 institutions in 2 countries.

Justin ZonnevilleDepartment of Cancer Genetics and Genomics, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Sean ColliganDepartment of Immunology, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Sydney GrantDepartment of Cancer Genetics and Genomics, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Alexandra MillerDrake University, Des Moines, Iowa, USA.
Paul WallaceDepartment of Flow & Image Cytometry, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Scott I AbramsDepartment of Immunology, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.ORCID 0000-0002-8742-4708
Andrei V BakinDepartment of Cancer Genetics and Genomics, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.ORCID 0000-0002-7728-1969
Roswell Park Comprehensive Cancer Center · USDrake University · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
CD28-mediated Regulation of Multiple Myeloma Cell Proliferation and SurvivalR01CA121044 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI LEE, KELVIN P. · 2007 to 2023
$4.8M
Summer Research Experiences in Quantitative Cancer Sciences and Emerging TechnologiesR25CA181003 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI PAMELA A HERSHBERGER, Mukund Seshadri · 2014 to 2026
$3.3M
MULTIDISCIPLINARY APPROACHES TUMOR IMMUNOLOGYT32CA085183 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI Scott I. Abrams · 2001 to 2026
$3.1M
Mechanisms Underlying Functional Programs of Tumor-Associated MacrophagesR01CA172105 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI ABRAMS, SCOTT I. · 2015 to 2019
$2.0M
Regulation of IRF8 in PMN-MDSC Development Within the Bone Marrow MicroenvironmentF31CA228396 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI COLLIGAN, SEAN · 2018 to 2020
$89k
NCI NIH HHS F31 CA228396NCI NIH HHS F31CA228396NCI NIH HHS P30 CA016056NCI NIH HHS R01 CA121044NCI NIH HHS R01 CA172105NCI NIH HHS R01CA172105NCI NIH HHS R25 CA181003NCI NIH HHS R25CA181003NCI NIH HHS T32 CA085183NCI NIH HHS T32CA085183
6 · The paper itself

Abstract

Patients with metastatic breast cancer (MBC) have limited therapeutic options and novel treatments are critically needed. Prior research implicates tumor-induced mobilization of myeloid cell populations in metastatic progression, as well as being an unfavorable outcome in MBC; however, the underlying mechanisms for these relationships remain unknown. Here, we provide evidence for a novel mechanism by which p38 promotes metastasis. Using triple-negative breast cancer models, we showed that a selective inhibitor of p38 (p38i) significantly reduced tumor growth, angiogenesis, and lung metastasis. Importantly, p38i decreased the accumulation of myeloid populations, namely, myeloid-derived suppressor cells (MDSCs) and CD163

Indexed as

AnimalsAntigens, CDAntigens, Differentiation, MyelomonocyticAntineoplastic AgentsCarcinogenesisCD163 AntigenCD8-Positive T-LymphocytesCell Line, TumorChemokinesCytokinesFemaleHumansLung NeoplasmsMacrophagesMAP Kinase Signaling SystemMiceAntigens, CDAntigens, Differentiation, MyelomonocyticAntineoplastic AgentsCD163 AntigenChemokinesCytokinesReceptors, Cell Surfacebreast cancermacrophagesmetastasismyeloid-derived suppressor cellsp38 kinasetumor microenvironment

Identifiers

PMID32452014
PMCPMC7484223
OpenAlexW3030658906

What OpenQuestion holds

Textmetadata
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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.