Evidence map›Paper›PMID 35993914›Full record

ArticleAngewandte Chemie (International ed. in English)2022

Enzyme-Activatable Chemokine Conjugates for In Vivo Targeting of Tumor-Associated Macrophages.

Nicole D Barth, Floris J Van Dalen, Utsa Karmakar, Marco Bertolini, Lorena Mendive-Tapia, Takanori Kitamura, Martijn Verdoes, Marc Vendrell

Open access · hybridAbstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 34 citations in OpenAlex.

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  12. Fluorogenic Granzyme A Substrates Enable Real-Time Imaging of Adaptive Immune Cell Activity.Angewandte Chemie (Weinheim an der Bergstrasse, Germany) · 2023
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  15. Enzyme-Activatable Chemokine Conjugates for In Vivo Targeting of Tumor-Associated Macrophages.Angewandte Chemie (Weinheim an der Bergstrasse, Germany) · 2022
    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

8 authors at 5 institutions in 3 countries.

Nicole D BarthCentre for Inflammation Research, University of Edinburgh, UK.
Floris J Van DalenDept. Tumor Immunology and Institute for Chemical Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, The Netherlands.
Utsa KarmakarCentre for Inflammation Research, University of Edinburgh, UK.
Marco BertoliniCentre for Inflammation Research, University of Edinburgh, UK.
Lorena Mendive-TapiaCentre for Inflammation Research, University of Edinburgh, UK.
Takanori KitamuraMRC Centre for Reproductive Health, University of Edinburgh, UK.
Martijn VerdoesDept. Tumor Immunology and Institute for Chemical Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, The Netherlands.ORCID 0000-0001-8753-3528
Marc VendrellCentre for Inflammation Research, University of Edinburgh, UK.ORCID 0000-0002-5392-9740
Centre for Inflammation Research · GBRadboud University Nijmegen · NLCentre de Recherche sur l'Inflammation · FREdinburgh Cancer Research · GBMRC Centre for Reproductive Health · GB

Funding

Medical Research Council MR/N022556/1Medical Research Council MR/S006982/1Wellcome TrustWellcome Trust 221647/Z/20/Z
6 · The paper itself

Abstract

Increased levels of tumor-associated macrophages (TAMs) are indicators of poor prognosis in most cancers. Although antibodies and small molecules blocking the recruitment of macrophages to tumors are under evaluation as anticancer therapies, these strategies are not specific for macrophage subpopulations. Herein we report the first enzyme-activatable chemokine conjugates for effective targeting of defined macrophage subsets in live tumors. Our constructs exploit the high expression of chemokine receptors (e.g., CCR2) and the activity of cysteine cathepsins in TAMs to target these cells selectively over other macrophages and immune cells (e.g., neutrophils, T cells, B cells). Furthermore, we demonstrate that cathepsin-activatable chemokines are compatible with both fluorescent and therapeutic cargos, opening new avenues in the design of targeted theranostic probes for immune cells in the tumor microenvironment.

Indexed as

CysteineTumor-Associated MacrophagesCathepsinsChemokinesReceptors, ChemokineTumor MicroenvironmentCathepsinsChemokinesCysteineReceptors, ChemokineCancerCathepsinsCCL2ProbesProdrugs

Identifiers

PMID35993914
PMCPMC9826351
OpenAlexW4292649285

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.