Evidence map›Paper›PMID 27980102›Full record

ArticleMolecular cancer therapeutics2017

Blocking the CCL2-CCR2 Axis Using CCL2-Neutralizing Antibody Is an Effective Therapy for Hepatocellular Cancer in a Mouse Model.

Kun-Yu Teng, Jianfeng Han, Xiaoli Zhang, Shu-Hao Hsu, Shun He, Nissar A Wani, Juan M Barajas, Linda A Snyder, Wendy L Frankel, Michael A Caligiuri and 3 more

Open access · greenAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

89 citing papers in PubMed, 132 citations in OpenAlex.

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29 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 3 institutions in 1 country.

Kun-Yu TengMolecular, Cellular and Developmental Biology Program, The Ohio State University, Columbus, Ohio.
Jianfeng HanComprehensive Cancer Center, Wexner Medical Center, The Ohio State University, Columbus, Ohio.
Xiaoli ZhangCenter for Biostatistics, The Ohio State University, Columbus, Ohio.
Shu-Hao HsuDepartment of Pathology, The Ohio State University, Columbus, Ohio.
Shun HeComprehensive Cancer Center, Wexner Medical Center, The Ohio State University, Columbus, Ohio.
Nissar A WaniDepartment of Pathology, The Ohio State University, Columbus, Ohio.
Juan M BarajasDepartment of Pathology, The Ohio State University, Columbus, Ohio.
Linda A SnyderJanssen Research and Development, LLC, Spring House, Pennsylvania.
Wendy L FrankelDepartment of Pathology, The Ohio State University, Columbus, Ohio.
Michael A CaligiuriComprehensive Cancer Center, Wexner Medical Center, The Ohio State University, Columbus, Ohio.
Samson T JacobComprehensive Cancer Center, Wexner Medical Center, The Ohio State University, Columbus, Ohio.
Jianhua YuComprehensive Cancer Center, Wexner Medical Center, The Ohio State University, Columbus, Ohio. kalpana.ghoshal@osumc.edu Jianhua.Yu@osumc.edu.
Kalpana GhoshalDepartment of Pathology, The Ohio State University, Columbus, Ohio. kalpana.ghoshal@osumc.edu Jianhua.Yu@osumc.edu.
The Ohio State University Wexner Medical Center · USSpringhouse · USThe Ohio State University · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
MOLECULAR MECHANISMS OF DIET-INDUCED CARCINOGENESISR01CA086978 · NCI · OHIO STATE UNIVERSITY · PI GHOSHAL, KALPANA, JACOB, SAMSON T · 2002 to 2018
$4.9M
Role of microR-122 in Hepatocarcinogenesis using Conditional Knockout MiceR01CA193244 · NCI · OHIO STATE UNIVERSITY · PI GHOSHAL, KALPANA · 2015 to 2019
$2.3M
Enhancing NK Cell Activity by Dietary Diphyllin Lignans for Cancer PreventionR01CA185301 · NCI · OHIO STATE UNIVERSITY · PI CALIGIURI, MICHAEL A, YU, JIANHUA · 2015 to 2019
$1.8M
Elucidate and Modulate TGF-b Signaling in NK Cells for Glioma TreatmentR01CA155521 · NCI · OHIO STATE UNIVERSITY · PI YU, JIANHUA · 2012 to 2014
$921k
NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA086978NCI NIH HHS R01 CA155521NCI NIH HHS R01 CA185301NCI NIH HHS R01 CA193244
6 · The paper itself

Abstract

Hepatocellular carcinoma, a deadly disease, commonly arises in the setting of chronic inflammation. C-C motif chemokine ligand 2 (CCL2/MCP1), a chemokine that recruits CCR2-positive immune cells to promote inflammation, is highly upregulated in hepatocellular carcinoma patients. Here, we examined the therapeutic efficacy of CCL2-CCR2 axis inhibitors against hepatitis and hepatocellular carcinoma in the miR-122 knockout (a.k.a. KO) mouse model. This mouse model displays upregulation of hepatic CCL2 expression, which correlates with hepatitis that progress to hepatocellular carcinoma with age. Therapeutic potential of CCL2-CCR2 axis blockade was determined by treating KO mice with a CCL2-neutralizing antibody (nAb). This immunotherapy suppressed chronic liver inflammation in these mice by reducing the population of CD11

Indexed as

AnimalsAntibodies, BlockingAntibodies, MonoclonalAntibodies, NeutralizingAntineoplastic AgentsBiomarkersBiopsyCarcinoma, HepatocellularCell Line, TumorCell Transformation, NeoplasticChemokine CCL2Disease Models, AnimalFlow CytometryGene ExpressionGene Expression Regulation, NeoplasticHumansAntibodies, BlockingAntibodies, MonoclonalAntibodies, NeutralizingAntineoplastic AgentsBiomarkersChemokine CCL2MicroRNAsMirn122 microRNA, mouseReceptors, CCR2

Identifiers

PMID27980102
PMCPMC5292068
OpenAlexW2564303203

What OpenQuestion holds

Textmetadata
LicenceTDM
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.