Evidence map›Paper›PMID 36923553›Full record

ArticleCancer research communications2022

Depletion of Mannose Receptor-Positive Tumor-associated Macrophages via a Peptide-targeted Star-shaped Polyglutamate Inhibits Breast Cancer Progression in Mice.

Anni Lepland, Alessio Malfanti, Uku Haljasorg, Eliana K Asciutto, Monica Pickholz, Mauro Bringas, Snežana Đorđević, Liis Salumäe, Pärt Peterson, Tambet Teesalu and 2 more

Open access · goldFull text read
In one paragraph

Article in Cancer research communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

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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

12 authors at 8 institutions in 4 countries.

Anni LeplandLaboratory of Precision and Nanomedicine, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.ORCID 0000-0002-6448-4847
Alessio MalfantiPolymer Therapeutics Laboratory, Prince Felipe Research Centre, Valencia, Spain.
Uku HaljasorgMolecular Pathology Research Group, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.ORCID 0000-0002-1541-6020
Eliana K AsciuttoSchool of Science and Technology, National University of San Martin (UNSAM) ICIFI and CONICET, Buenos Aires, Argentina.ORCID 0000-0002-8931-027X
Monica PickholzDepartamento de Física, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina.ORCID 0000-0002-0172-2748
Mauro BringasDepartamento de Química Inorgánica, Analítica y Química Física, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina.ORCID 0000-0002-2040-3689
Snežana ĐorđevićPolymer Therapeutics Laboratory, Prince Felipe Research Centre, Valencia, Spain.ORCID 0000-0001-8429-7486
Liis SalumäePathology Department, Tartu University Hospital, Tartu, Estonia.
Pärt PetersonMolecular Pathology Research Group, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.ORCID 0000-0001-6755-791X
Tambet TeesaluLaboratory of Precision and Nanomedicine, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
María J VicentPolymer Therapeutics Laboratory, Prince Felipe Research Centre, Valencia, Spain.ORCID 0000-0001-7771-3373
Pablo ScodellerLaboratory of Precision and Nanomedicine, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.ORCID 0000-0003-0745-2467
Centro de Investigacion Principe Felipe · ESUniversity of Tartu · EECentro Nacional de Biotecnología · ESFundación Instituto Leloir · ARNational University of General San Martín · ARTartu University Hospital · EEUniversidad de Buenos Aires · ARUniversity of California, Santa Barbara · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although many studies have explored the depletion of tumor-associated macrophages (TAM) as a therapeutic strategy for solid tumors, currently available compounds suffer from poor efficacy and dose-limiting side effects. Here, we developed a novel TAM-depleting agent ("OximUNO") that specifically targets CD206 Significance: A peptide-targeted nanoformulation of DOX exclusively eliminates mannose receptor+ TAMs in breast cancer models, generating response without off-target effects (a drawback of many TAM-depleting agents under clinical study).

Indexed as

Mannose ReceptorTriple Negative Breast NeoplasmsAnimalsDoxorubicinHumansMacrophagesMiceNeoplastic ProcessesPeptidesPolyglutamic AcidTumor-Associated MacrophagesDoxorubicinMannose ReceptorPeptidesPolyglutamic Acid

Identifiers

PMID36923553
PMCPMC10010335
OpenAlexW4282828362

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read153
identifiers read3
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.