Evidence map›Paper›PMID 38362405›Full record

ArticleChemical science2024

Polarization of macrophages to an anti-cancer phenotype through

Xianzhi Zhang, Yuanchang Liu, Mingdi Jiang, Javier A Mas-Rosario, Stefano Fedeli, Roberto Cao-Milan, Liang Liu, Kyle J Winters, Cristina-Maria Hirschbiegel, Ahmed Nabawy and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Chemical science, 2024. 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
4.8field-weighted citation impact, top 4% 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, 26 citations in OpenAlex.

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  7. Cu single-atom embedded g-CNature communications · 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

13 authors at 1 institution in 1 country.

Xianzhi ZhangDepartment of Chemistry, University of Massachusetts Amherst 710 N. Pleasant St. Amherst MA 01003 USA rotello@chem.umass.edu.ORCID https://orcid.org/0000-0002-9585-7458
Yuanchang LiuDepartment of Chemistry, University of Massachusetts Amherst 710 N. Pleasant St. Amherst MA 01003 USA rotello@chem.umass.edu.
Mingdi JiangDepartment of Chemistry, University of Massachusetts Amherst 710 N. Pleasant St. Amherst MA 01003 USA rotello@chem.umass.edu.ORCID https://orcid.org/0000-0002-4742-405X
Javier A Mas-RosarioDepartment of Chemistry, University of Massachusetts Amherst 710 N. Pleasant St. Amherst MA 01003 USA rotello@chem.umass.edu.
Stefano FedeliDepartment of Chemistry, University of Massachusetts Amherst 710 N. Pleasant St. Amherst MA 01003 USA rotello@chem.umass.edu.
Roberto Cao-MilanDepartment of Chemistry, University of Massachusetts Amherst 710 N. Pleasant St. Amherst MA 01003 USA rotello@chem.umass.edu.
Liang LiuDepartment of Chemistry, University of Massachusetts Amherst 710 N. Pleasant St. Amherst MA 01003 USA rotello@chem.umass.edu.
Kyle J WintersDepartment of Chemistry, University of Massachusetts Amherst 710 N. Pleasant St. Amherst MA 01003 USA rotello@chem.umass.edu.
Cristina-Maria HirschbiegelDepartment of Chemistry, University of Massachusetts Amherst 710 N. Pleasant St. Amherst MA 01003 USA rotello@chem.umass.edu.ORCID https://orcid.org/0000-0003-2835-513X
Ahmed NabawyDepartment of Chemistry, University of Massachusetts Amherst 710 N. Pleasant St. Amherst MA 01003 USA rotello@chem.umass.edu.ORCID https://orcid.org/0000-0001-6505-4606
Rui HuangDepartment of Chemistry, University of Massachusetts Amherst 710 N. Pleasant St. Amherst MA 01003 USA rotello@chem.umass.edu.
Michelle E FarkasDepartment of Chemistry, University of Massachusetts Amherst 710 N. Pleasant St. Amherst MA 01003 USA rotello@chem.umass.edu.ORCID https://orcid.org/0000-0001-5824-1243
Vincent M RotelloDepartment of Chemistry, University of Massachusetts Amherst 710 N. Pleasant St. Amherst MA 01003 USA rotello@chem.umass.edu.ORCID https://orcid.org/0000-0002-5184-5439
University of Massachusetts Amherst · US

Funding

Chemistry-Biology Interface Predoctoral Training GrantT32GM139789 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI ERIC Robert STRIETER · 2021 to 2026
$3.4M
NIGMS NIH HHS T32 GM139789
6 · The paper itself

Abstract

Macrophages are plastic cells of the immune system that can be broadly classified as having pro-inflammatory (M1-like) or anti-inflammatory (M2-like) phenotypes. M2-like macrophages are often associated with cancers and can promote cancer growth and create an immune-suppressive tumor microenvironment. Repolarizing macrophages from M2-like to M1-like phenotype provides a crucial strategy for anticancer immunotherapy. Imiquimod is an FDA-approved small molecule that can polarize macrophages by activating toll-like receptor 7/8 (TLR 7/8) located inside lysosomes. However, the non-specific inflammation that results from the drug has limited its systemic application. To overcome this issue, we report the use of gold nanoparticle-based bioorthogonal nanozymes for the conversion of an inactive, imiquimod-based prodrug to an active compound for macrophage re-education from anti- to pro-inflammatory phenotypes. The nanozymes were delivered to macrophages through endocytosis, where they uncaged pro-imiquimod

Identifiers

PMID38362405
PMCPMC10866364
OpenAlexW4390771552

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.