Evidence map›Paper›PMID 33169982›Full record

ArticleACS applied materials & interfaces2020

Targeting Tumor-Associated Macrophages by MMP2-Sensitive Apoptotic Body-Mimicking Nanoparticles.

Yin Liu, Jiao Wang, Jian Zhang, Sandra Marbach, Wei Xu, Lin Zhu

Open access · greenAbstract read
In one paragraph

Article in ACS applied materials & interfaces, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 53 citations in OpenAlex.

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  12. Smart Tumor Cell-Derived DNA Nano-Tree Assembly for On-Demand Macrophages Reprogramming.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
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  17. Ghost messages: cell death signals spread.Cell communication and signaling : CCS · 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

6 authors at 2 institutions in 1 country.

Yin LiuDepartment of Pharmaceutical Sciences, Irma Lerma Rangel College of Pharmacy, Texas A&M University College Station, Kingsville 78363, Texas, United States.ORCID http://orcid.org/0000-0001-9112-5252
Jiao WangDepartment of Pharmaceutical Sciences, Irma Lerma Rangel College of Pharmacy, Texas A&M University College Station, Kingsville 78363, Texas, United States.
Jian ZhangDepartment of Pharmaceutical Sciences, Irma Lerma Rangel College of Pharmacy, Texas A&M University College Station, Kingsville 78363, Texas, United States.
Sandra MarbachDepartment of Life Sciences, College of Science and Engineering, Texas A&M University, Corpus Christi 78412, Texas, United States.
Wei XuDepartment of Life Sciences, College of Science and Engineering, Texas A&M University, Corpus Christi 78412, Texas, United States.
Lin ZhuDepartment of Pharmaceutical Sciences, Irma Lerma Rangel College of Pharmacy, Texas A&M University College Station, Kingsville 78363, Texas, United States.ORCID http://orcid.org/0000-0002-4047-1726
Texas A&M University – Kingsville · USTexas A&M University – Corpus Christi · US

Funding

Improving tumor specificity and overcoming drug resistance of proteasome inhibitors by a dual-targeted drug delivery systemR15CA213103 · NCI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ZHU, LIN · 2018 to 2018
$444k
NCI NIH HHS R15 CA213103
6 · The paper itself

Abstract

Tumor-associated macrophages (TAMs), a major player in the tumor microenvironment, were recently recognized as a potential therapeutic target. To date, very few anticancer drugs or drug-delivery systems were designed to target the TAMs. Inspired by the "eat me" signal, phosphatidylserine (PS), mediated phagocytic clearance of apoptotic bodies, in this study, the matrix metalloproteinase 2 (MMP2)-sensitive PS-modified nanoparticles were developed. In the design, the PS is externalized to the nanoparticles' surface only when the nanoparticles reach the MMP2-overexpressing tumor site, allowing for the TAM-specific phagocytosis. The nanoparticles' excellent macrophage/TAM selectivity was observed in various biological models, including various cell lines, coculture cells, coculture cell spheroids, zebrafish, and tumor-bearing mice. The nanoparticles' TAM specificity remarkably enhanced the TAM depletion capability of the loaded model drug, dasatinib, resulting in the improved anticancer activity. The MMP2-sensitive apoptotic body-mimicking nanoparticles might be a promising delivery tool for TAM-centered cancer diagnoses and treatments.

Indexed as

ApoptosisAnimalsAntineoplastic AgentsCell Line, TumorDasatinibFemaleHumansLarvaMatrix Metalloproteinase 2MiceMice, Inbred BALB CNanoparticlesNeoplasmsPhagocytosisPhosphatidylserinesPolyethylene GlycolsAntineoplastic AgentsDasatinibMatrix Metalloproteinase 2PhosphatidylserinesPolyethylene Glycolsapoptotic bodydrug deliverymatrix metalloproteinase 2nanoparticlesphosphatidylserinetumor-associated macrophages

Identifiers

PMID33169982
PMCPMC8229024
OpenAlexW3101496447

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.