Evidence map›Paper›PMID 32025027›Full record

ArticleBritish journal of cancer2020

Ibrutinib treatment inhibits breast cancer progression and metastasis by inducing conversion of myeloid-derived suppressor cells to dendritic cells.

Sanjay Varikuti, Bhawana Singh, Greta Volpedo, Dinesh K Ahirwar, Bijay K Jha, Noushin Saljoughian, Agostinho G Viana, Chaitenya Verma, Omar Hamza, Gregory Halsey and 5 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 5% 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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

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  13. Immune Microenvironment in Breast Cancer Metastasis.Advances in experimental medicine and biology · 2025
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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

15 authors at 2 institutions in 1 country.

Sanjay Varikuti *Department of Pathology, The Ohio State University Medical Center, Columbus, OH, USA.
Bhawana Singh *Department of Pathology, The Ohio State University Medical Center, Columbus, OH, USA.
Greta VolpedoDepartment of Pathology, The Ohio State University Medical Center, Columbus, OH, USA.
Dinesh K AhirwarDepartment of Pathology, The Ohio State University Medical Center, Columbus, OH, USA.
Bijay K JhaDepartment of Infection and Immunity, The Ohio State University, Columbus, OH, USA.
Noushin SaljoughianDepartment of Pathology, The Ohio State University Medical Center, Columbus, OH, USA.
Agostinho G VianaDepartment of Pathology, The Ohio State University Medical Center, Columbus, OH, USA.
Chaitenya VermaDepartment of Pathology, The Ohio State University Medical Center, Columbus, OH, USA.
Omar HamzaDepartment of Pathology, The Ohio State University Medical Center, Columbus, OH, USA.
Gregory HalseyDepartment of Pathology, The Ohio State University Medical Center, Columbus, OH, USA.
Erin A HolcombDepartment of Pathology, The Ohio State University Medical Center, Columbus, OH, USA.
Ritvik J MaryalaDepartment of Pathology, The Ohio State University Medical Center, Columbus, OH, USA.
Steve OghumuDepartment of Pathology, The Ohio State University Medical Center, Columbus, OH, USA.
Ramesh K GanjuDepartment of Pathology, The Ohio State University Medical Center, Columbus, OH, USA.
Abhay R SatoskarDepartment of Pathology, The Ohio State University Medical Center, Columbus, OH, USA. abhay.satoskar@osumc.edu.
The Ohio State University · USThe Ohio State University Wexner Medical Center · US

Funding

Mechanisms of Oral Cancer Inhibition by Bioactive Phytochemicals in Black RaspberriesK01CA207599 · NCI · OHIO STATE UNIVERSITY · PI OGHUMU, STEVE ONYEKA · 2017 to 2021
$715k
NCI NIH HHS K01 CA207599
6 · The paper itself

Abstract

backgroundIbrutinib is a Bruton's tyrosine kinase (BTK) and interleukin-2-inducible kinase (ITK) inhibitor used for treating chronic lymphocytic leukaemia (CLL) and other cancers. Although ibrutinib is known to inhibit the growth of breast cancer cell growth in vitro, its impact on the treatment and metastasis of breast cancer is unclear.

methodsUsing an orthotopic mouse breast cancer model, we show that ibrutinib inhibits the progression and metastasis of breast cancer.

resultsIbrutinib inhibited proliferation of cancer cells in vitro, and Ibrutinib-treated mice displayed significantly lower tumour burdens and metastasis compared to controls. Furthermore, the spleens and tumours from Ibrutinib-treated mice contained more mature DCs and lower numbers of myeloid-derived suppressor cells (MDSCs), which promote disease progression and are linked to poor prognosis. We also confirmed that ex vivo treatment of MDSCs with ibrutinib switched their phenotype to mature DCs and significantly enhanced MHCII expression. Further, ibrutinib treatment promoted T cell proliferation and effector functions leading to the induction of antitumour T

conclusionsIbrutinib inhibits tumour development and metastasis in breast cancer by promoting the development of mature DCs from MDSCs and hence could be a novel therapeutic agent for the treatment of breast cancer.

Indexed as

AdenineAnimalsBreast NeoplasmsDendritic CellsDisease ProgressionFemaleHumansMiceMyeloid-Derived Suppressor CellsNeoplasm MetastasisPiperidinesAdenineibrutinibPiperidines

Identifiers

PMID32025027
PMCPMC7109110
OpenAlexW3005025575

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.