Evidence map›Paper›PMID 33682324›Full record

ArticleMolecular oncology2021

Therapeutic targeting with DABIL-4 depletes myeloid suppressor cells in 4T1 triple-negative breast cancer model.

Sadiya Parveen, Sumit Siddharth, Laurene S Cheung, Alok Kumar, Jessica Shen, John R Murphy, Dipali Sharma, William R Bishai

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Tumor-Associated Macrophage in Breast Tumor Microenvironment.International journal of molecular sciences · 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

8 authors at 1 institution in 1 country.

Sadiya ParveenDepartment of Medicine, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Sumit SiddharthDepartment of Oncology, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Laurene S CheungDepartment of Medicine, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Alok KumarDepartment of Medicine, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Jessica ShenDepartment of Medicine, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
John R MurphyDepartment of Medicine, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Dipali SharmaDepartment of Oncology, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
William R BishaiDepartment of Medicine, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, USA.ORCID 0000-0002-8734-4118
Johns Hopkins University · US

Funding

Targeted cell-depleting immunotherapy for TB and HIVR01AI152688 · NIAID · JOHNS HOPKINS UNIVERSITY · PI BISHAI, WILLIAM RAMSES · 2020 to 2024
$3.4M
Treg-depleting immunotherapyR44CA254764 · NCI · SONOVAL LLC · PI BISHAI, WILLIAM RAMSES, SUZDAK, PETER DAVID · 2020 to 2022
$2.3M
Targeted Immunotherapy for Tuberculosis and HIV co-infectionR21AI130595 · NIAID · JOHNS HOPKINS UNIVERSITY · PI BISHAI, WILLIAM RAMSES · 2017 to 2018
$449k
NCI NIH HHS R44 CA254764NIAID NIH HHS R01 AI152688NIAID NIH HHS R21 AI130595
6 · The paper itself

Abstract

In many solid tumors including triple-negative breast cancer (TNBC), upregulation of the interleukin-4 receptor (IL-4R) has been shown to promote cancer cell proliferation, apoptotic resistance, metastatic potential, and a Th2 response in the tumor microenvironment (TME). Since immunosuppressive cells in the TME and spleen including myeloid-derived suppressor cells (MDSCs) and tumor-associated macrophages (TAMs) also express the IL-4R, we hypothesized that selective depletion of IL-4R-bearing cells in TNBC would result in the direct killing of tumor cells and the depletion of immunosuppressive cells and lead to an enhanced antitumor response. To selectively target IL-4R

Indexed as

AdenocarcinomaAnimalsAntineoplastic AgentsApoptosisCell CountCell Line, TumorFemaleHumansInterleukin-4Interleukin-4 Receptor alpha SubunitMiceMice, Inbred BALB CMice, KnockoutMolecular Targeted TherapyMyeloid-Derived Suppressor CellsRecombinant Fusion ProteinsAntineoplastic AgentsIL4R protein, humanInterleukin-4Interleukin-4 Receptor alpha SubunitRecombinant Fusion ProteinsDABIL-4diphtheria fusion toxinIL-4Rmyeloid-derived suppressor cellstriple-negative breast cancertumor-associated macrophages

Identifiers

PMID33682324
PMCPMC8096791
OpenAlexW3134641697

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.