Evidence map›Paper›PMID 34060472›Full record

ArticleeLife2021

Targeting a cell surface vitamin D receptor on tumor-associated macrophages in triple-negative breast cancer.

Fernanda I Staquicini, Amin Hajitou, Wouter Hp Driessen, Bettina Proneth, Marina Cardó-Vila, Daniela I Staquicini, Christopher Markosian, Maria Hoh, Mauro Cortez, Anupama Hooda-Nehra and 20 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 33 citations in OpenAlex.

  1. Phage Display as a Promising Platform for Peptide Drug Discovery.Pharmaceuticals (Basel, Switzerland) · 2026
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  13. Ceramide as an endothelial cell surface receptor and a lung-specific lipid vascular target for circulating ligands.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

30 authors at 14 institutions in 5 countries.

Fernanda I StaquiciniRutgers Cancer Institute of New Jersey, Newark, United States.ORCID 0000-0003-1137-6575
Amin HajitouPhage Therapy Group, Department of Brain Sciences, Imperial College London, London, United Kingdom.
Wouter Hp DriessenThe University of Texas M.D. Anderson Cancer Center, Houston, United States.
Bettina PronethInstitute of Metabolism and Cell Death, Helmholtz Zentrum Muenchen, Neuherberg, Germany.
Marina Cardó-VilaDepartment of Cellular and Molecular Medicine, The University of Arizona Cancer Center, University of Arizona, Tucson, United States.
Daniela I StaquiciniRutgers Cancer Institute of New Jersey, Newark, United States.
Christopher MarkosianRutgers Cancer Institute of New Jersey, Newark, United States.
Maria HohDivision of Cancer Imaging Research, The Russell H Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, United States.
Mauro CortezDepartment of Parasitology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil.ORCID 0000-0001-6536-4647
Anupama Hooda-NehraRutgers Cancer Institute of New Jersey, Newark, United States.
Mohammed JaloudiRutgers Cancer Institute of New Jersey, Newark, United States.
Israel T SilvaLaboratory of Computational Biology, A.C. Camargo Cancer Center, São Paulo, Brazil.
Jaqueline ButturaLaboratory of Computational Biology, A.C. Camargo Cancer Center, São Paulo, Brazil.
Diana N NunesLaboratory of Medical Genomics, A.C. Camargo Cancer Center, São Paulo, Brazil.
Emmanuel Dias-NetoLaboratory of Computational Biology, A.C. Camargo Cancer Center, São Paulo, Brazil.
Bedrich EckhardtTranslational Breast Cancer Program, Olivia Newton-John Cancer Research Institute, Melbourne, Australia.
Javier Ruiz-RamírezMathematics in Medicine Program, The Houston Methodist Research Institute, Houston, United States.
Prashant DograMathematics in Medicine Program, The Houston Methodist Research Institute, Houston, United States.
Zhihui WangMathematics in Medicine Program, The Houston Methodist Research Institute, Houston, United States.
Vittorio CristiniMathematics in Medicine Program, The Houston Methodist Research Institute, Houston, United States.
Martin TrepelDepartment of Oncology and Hematology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Robin AndersonTranslational Breast Cancer Program, Olivia Newton-John Cancer Research Institute, Melbourne, Australia.
Richard L SidmanDepartment of Neurology, Harvard Medical School, Boston, United States.
Juri G GelovaniDepartment of Biomedical Engineering, College of Engineering, Wayne State University, Detroit, United States.
Massimo CristofanilliRobert H Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University Chicago, Chicago, United States.
Gabriel N HortobagyiDepartment of Breast Medical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, United States.
Zaver M BhujwallaDivision of Cancer Imaging Research, The Russell H Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, United States.
Stephen K BurleyRutgers Cancer Institute of New Jersey, New Brunswick, United States.
Wadih Arap *Rutgers Cancer Institute of New Jersey, Newark, United States.ORCID 0000-0002-8686-4584
Renata Pasqualini *Rutgers Cancer Institute of New Jersey, Newark, United States.
Rutgers, The State University of New Jersey · USAC Camargo Hospital · BRHouston Methodist · USJohns Hopkins University · USOlivia Newton-John Cancer Wellness & Research Centre · AUThe University of Texas MD Anderson Cancer Center · USHarvard University · USHelmholtz Zentrum München · DEImperial College London · GBNorthwestern University · USUniversidade de São Paulo · BRUniversität Hamburg · DEUniversity of Arizona · USWayne State University · US

Funding

PDB MANAGEMENT BY THE RESEARCH COLLABORATORY FOR STRUCTURAL BIOINFORMATICSR01GM133198 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI BURLEY, STEPHEN K · 2019 to 2023
$19.3M
Transport Oncophysics CoreU54CA210181 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI CHANG, JENNY C-N, SHEN, HAIFA · 2016 to 2020
$9.3M
Imaging and Molecular Correlates of Progression in Cystic Neoplasms of the PancreasU01CA196403 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MAITRA, ANIRBAN · 2015 to 2020
$5.8M
A Targeted Nanomedicine Prototype Against Enzalutamide-resistant Prostate CancerR01CA226537 · NCI · RBHS -CANCER INSTITUTE OF NEW JERSEY · PI ARAP, WADIH, BRINKER, C JEFFREY · 2018 to 2022
$3.2M
miR-155 targeted therapeutics for precision medicine in lung cancerR01CA222007 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CALIN, GEORGE A., CRISTINI, VITTORIO · 2018 to 2022
$2.6M
Targeted therapeutics for ovarian cancer and its microenvironment - treatment and theoretical modelingU01CA213759 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LOPEZ-BERESTEIN, GABRIEL · 2017 to 2021
$2.5M
Cancer Research UK 25887Medical Research Council G0701159Medical Research Council MR/T029226/1NCI NIH HHS R01 CA222007NCI NIH HHS R01 CA226537NCI NIH HHS U01 CA196403NCI NIH HHS U01 CA213759NCI NIH HHS U54 CA210181NIGMS NIH HHS R01 GM133198
6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is an aggressive tumor with limited treatment options and poor prognosis. We applied the in vivo phage display technology to isolate peptides homing to the immunosuppressive cellular microenvironment of TNBC as a strategy for non-malignant target discovery. We identified a cyclic peptide (CSSTRESAC) that specifically binds to a vitamin D receptor, protein disulfide-isomerase A3 (PDIA3) expressed on the cell surface of tumor-associated macrophages (TAM), and targets breast cancer in syngeneic TNBC, non-TNBC xenograft, and transgenic mouse models. Systemic administration of CSSTRESAC to TNBC-bearing mice shifted the cytokine profile toward an antitumor immune response and delayed tumor growth. Moreover, CSSTRESAC enabled ligand-directed theranostic delivery to tumors and a mathematical model confirmed our experimental findings. Finally, in silico analysis showed PDIA3-expressing TAM in TNBC patients. This work uncovers a functional interplay between a cell surface vitamin D receptor in TAM and antitumor immune response that could be therapeutically exploited.

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorEnzyme ActivationFemaleGene Expression Regulation, NeoplasticHumansLigandsMiceMice, Inbred BALB CMice, NudeModels, BiologicalOligopeptidesProtein Disulfide-IsomerasesSignal TransductionTriple Negative Breast NeoplasmsAntineoplastic AgentsLigandsOligopeptidesPDIA3 protein, humanPdia3 protein, mouseProtein Disulfide-IsomerasesVitamin D-Binding Proteinmedicinemousetriple-negative breast cancertumor-associated macrophagevitamin D receptor

Identifiers

PMID34060472
PMCPMC8169110
OpenAlexW3164691047

What OpenQuestion holds

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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.