Evidence map›Paper›PMID 30139814›Full record

ArticleCancer research2018

Inhibition of Casein Kinase 2 Disrupts Differentiation of Myeloid Cells in Cancer and Enhances the Efficacy of Immunotherapy in Mice.

Ayumi Hashimoto, Chan Gao, Jerome Mastio, Andrew Kossenkov, Scott I Abrams, Ashok V Purandare, Heshani Desilva, Susan Wee, John Hunt, Maria Jure-Kunkel and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
4.4field-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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

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  17. Protein Kinase CK2 Regulates B Cell Development and Differentiation.Journal of immunology (Baltimore, Md. : 1950) · 2021
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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

11 authors at 1 institution in 1 country.

Ayumi HashimotoWistar Institute, Philadelphia, Pennsylvania.
Chan GaoBristol-Myers Squibb, Princeton, New Jersey.
Jerome MastioWistar Institute, Philadelphia, Pennsylvania.
Andrew KossenkovWistar Institute, Philadelphia, Pennsylvania.
Scott I AbramsRoswell Park Comprehensive Cancer Center, Department of Immunology, Buffalo, New York, Medimmune, Gaithersburg, Maryland.
Ashok V PurandareBristol-Myers Squibb, Princeton, New Jersey.
Heshani DesilvaBristol-Myers Squibb, Princeton, New Jersey.
Susan WeeBristol-Myers Squibb, Princeton, New Jersey.
John Hunt
Maria Jure-KunkelBristol-Myers Squibb, Princeton, New Jersey.
Dmitry I GabrilovichWistar Institute, Philadelphia, Pennsylvania. dgabrilovich@wistar.org.
Bristol-Myers Squibb (United States) · US

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
Correction of myeloid cell defects in cancerR01CA084488 · NCI · WISTAR INSTITUTE · PI GABRILOVICH, DMITRY I · 1999 to 2017
$5.4M
Mechanism of myeloid cell defect in cancerR01CA100062 · NCI · WISTAR INSTITUTE · PI GABRILOVICH, DMITRY I · 2004 to 2018
$4.0M
Integrative Approach to Comprehensive Analysis of High Throughput Data on a Cancer Center LevelR50CA211199 · NCI · WISTAR INSTITUTE · PI Andrew V Kossenkov · 2016 to 2026
$1.6M
Purchase a Beckman Coulter MoFlo Astrios Flow CytometerS10OD017998 · OD · WISTAR INSTITUTE · PI MONTANER, LUIS J · 2014 to 2014
$595k
NCI NIH HHS P30 CA010815NCI NIH HHS R01 CA084488NCI NIH HHS R01 CA100062NCI NIH HHS R50 CA211199NIH HHS S10 OD017998
6 · The paper itself

Abstract

The role of myeloid cells as regulators of tumor progression that significantly impact the efficacy of cancer immunotherapies makes them an attractive target for inhibition. Here we explore the effect of a novel, potent, and selective inhibitor of serine/threonine protein kinase casein kinase 2 (CK2) on modulating myeloid cells in the tumor microenvironment. Although inhibition of CK2 caused only a modest effect on dendritic cells in tumor-bearing mice, it substantially reduced the amount of polymorphonuclear myeloid-derived suppressor cells and tumor-associated macrophages. This effect was not caused by the induction of apoptosis, but rather by a block of differentiation. Our results implicated downregulation of CCAAT-enhancer binding protein-α in this effect. Although CK2 inhibition did not directly affect tumor cells, it dramatically enhanced the antitumor activity of immune checkpoint receptor blockade using anti-CTLA-4 antibody. These results suggest a potential role of CK2 inhibitors in combination therapies against cancer.

Indexed as

ImmunotherapyAnimalsAntineoplastic AgentsApoptosisCasein Kinase IICCAAT-Enhancer-Binding ProteinsCell DifferentiationCell Line, TumorCTLA-4 AntigenFemaleFetal BloodHematopoietic Stem CellsHumansMacrophagesMiceMice, Inbred BALB CAntineoplastic AgentsCasein Kinase IICCAAT-Enhancer-Binding ProteinsCEBPA protein, mouseCTLA-4 AntigenCTLA4 protein, human

Identifiers

PMID30139814
PMCPMC6168407
OpenAlexW2888667754

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.