Evidence map›Paper›PMID 37646133›Full record

ArticleBiomaterials science2023

ICAM-1-decorated extracellular vesicles loaded with miR-146a and

Silvia Duarte-Sanmiguel, Ana I Salazar-Puerta, Ana Panic, Daniel Dodd, Carlie Francis, Diego Alzate-Correa, Lilibeth Ortega-Pineda, Luke Lemmerman, Maria A Rincon-Benavides, Kavya Dathathreya and 12 more

Open access · greenAbstract read
In one paragraph

Article in Biomaterials science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 22 citations in OpenAlex.

  1. Isolation of Extracellular Vesicles From Mouse Brown Adipose Tissue Secretome Using Size-Exclusion Chromatography.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
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  6. Rewiring cell identityNanomedicine (London, England) · 2025
    Article
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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

22 authors at 3 institutions in 2 countries.

Silvia Duarte-SanmiguelThe Ohio State University, Department of Biomedical Engineering, Columbus, OH 43210, USA. gallegoperez.1@osu.edu.
Ana I Salazar-PuertaThe Ohio State University, Department of Biomedical Engineering, Columbus, OH 43210, USA. gallegoperez.1@osu.edu.
Ana PanicThe Ohio State University, Department of Biomedical Engineering, Columbus, OH 43210, USA. gallegoperez.1@osu.edu.
Daniel DoddThe Ohio State University, Department of Biomedical Engineering, Columbus, OH 43210, USA. gallegoperez.1@osu.edu.ORCID http://orcid.org/0000-0003-4095-053X
Carlie FrancisThe Ohio State University, Department of Biomedical Engineering, Columbus, OH 43210, USA. gallegoperez.1@osu.edu.
Diego Alzate-CorreaThe Ohio State University, Department of Biomedical Engineering, Columbus, OH 43210, USA. gallegoperez.1@osu.edu.
Lilibeth Ortega-PinedaThe Ohio State University, Department of Biomedical Engineering, Columbus, OH 43210, USA. gallegoperez.1@osu.edu.
Luke LemmermanThe Ohio State University, Department of Biomedical Engineering, Columbus, OH 43210, USA. gallegoperez.1@osu.edu.
Maria A Rincon-BenavidesThe Ohio State University, Department of Biomedical Engineering, Columbus, OH 43210, USA. gallegoperez.1@osu.edu.
Kavya DathathreyaThe Ohio State University, Department of Biomedical Engineering, Columbus, OH 43210, USA. gallegoperez.1@osu.edu.
William LawrenceThe Ohio State University, Department of Biomedical Engineering, Columbus, OH 43210, USA. gallegoperez.1@osu.edu.ORCID http://orcid.org/0000-0001-8639-3420
Neil OttThe Ohio State University, Department of Biomedical Engineering, Columbus, OH 43210, USA. gallegoperez.1@osu.edu.
Jingjing ZhangThe Ohio State University, William G. Lowrie Department of Chemical and Biomolecular Engineering, Columbus, OH 43210, USA.
Binbin DengThe Ohio State University, Center for Electron Microscopy and Microanalysis (CEMAS), Columbus, OH 43210, USA.
Shipeng WangThe Ohio State University, Department of Biomedical Engineering, Columbus, OH 43210, USA. gallegoperez.1@osu.edu.
Sandra P SantanderJuan N. Corpas University Foundation, Center of Phytoimmunomodulation Department of Medicine, Bogota, Colombia.ORCID http://orcid.org/0000-0002-1211-1010
David W McCombThe Ohio State University, Center for Electron Microscopy and Microanalysis (CEMAS), Columbus, OH 43210, USA.
Eduardo ReateguiThe Ohio State University, William G. Lowrie Department of Chemical and Biomolecular Engineering, Columbus, OH 43210, USA.
Andre F PalmerThe Ohio State University, William G. Lowrie Department of Chemical and Biomolecular Engineering, Columbus, OH 43210, USA.
William E CarsonThe Ohio State University, Department of Surgery, Columbus, OH 43210, USA.
Natalia Higuita-CastroThe Ohio State University, Department of Biomedical Engineering, Columbus, OH 43210, USA. gallegoperez.1@osu.edu.
Daniel Gallego-PerezThe Ohio State University, Department of Biomedical Engineering, Columbus, OH 43210, USA. gallegoperez.1@osu.edu.ORCID http://orcid.org/0000-0002-6263-3191
The Ohio State University · USLung Institute · USFundación Universitaria Juan N. Corpas · CO

Funding

Novel nanoscale approaches to whole tissue reprogrammingDP2EB028110 · NIBIB · OHIO STATE UNIVERSITY · PI GALLEGO-PEREZ, DANIEL · 2018 to 2022
$2.7M
NIBIB NIH HHS DP2 EB028110
6 · The paper itself

Abstract

Tumor-associated immune cells play a crucial role in cancer progression. Myeloid-derived suppressor cells (MDSCs), for example, are immature innate immune cells that infiltrate the tumor to exert immunosuppressive activity and protect cancer cells from the host's immune system and/or cancer-specific immunotherapies. While tumor-associated immune cells have emerged as a promising therapeutic target, efforts to counter immunosuppression within the tumor niche have been hampered by the lack of approaches that selectively target the immune cell compartment of the tumor, to effectively eliminate "tumor-protecting" immune cells and/or drive an "anti-tumor" phenotype. Here we report on a novel nanotechnology-based approach to target tumor-associated immune cells and promote "anti-tumor" responses in a murine model of breast cancer. Engineered extracellular vesicles (EVs) decorated with ICAM-1 ligands and loaded with miR-146a and

Indexed as

Extracellular VesiclesGlucose Transporter Type 1ImmunomodulationIntercellular Adhesion Molecule-1MicroRNAsAnimalsBreast NeoplasmsCell Line, TumorDisease ProgressionFemaleHumansMiceMice, Inbred BALB CMyeloid-Derived Suppressor CellsGlucose Transporter Type 1Intercellular Adhesion Molecule-1MicroRNAsMirn146 microRNA, mouseSlc2a1 protein, mouse

Identifiers

PMID37646133
PMCPMC10591940
OpenAlexW4386271740

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.