Evidence map›Paper›PMID 29536600›Full record

ArticleAngewandte Chemie (International ed. in English)2018

Enzyme-MOF Nanoreactor Activates Nontoxic Paracetamol for Cancer Therapy.

Xizhen Lian, Yanyan Huang, Yuanyuan Zhu, Yu Fang, Rui Zhao, Elizabeth Joseph, Jialuo Li, Jean-Philippe Pellois, Hong-Cai Zhou

Open access · greenAbstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
13.4field-weighted citation impact, top 1% 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

49 citing papers in PubMed, 274 citations in OpenAlex.

  1. Article
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  9. Nanoparticle-Based Immunotherapy for Reversing T-Cell Exhaustion.International journal of molecular sciences · 2024
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Metal-Organic Framework (MOF)-A Universal Material for Biomedicine.International journal of molecular sciences · 2023
    Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Review
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

9 authors at 2 institutions in 2 countries.

Xizhen LianDepartment of Chemistry, Texas A&M University, College Station, TX, 77843-3255, USA.
Yanyan HuangBeijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
Yuanyuan ZhuBeijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
Yu FangDepartment of Chemistry, Texas A&M University, College Station, TX, 77843-3255, USA.
Rui ZhaoBeijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
Elizabeth JosephDepartment of Chemistry, Texas A&M University, College Station, TX, 77843-3255, USA.
Jialuo LiDepartment of Chemistry, Texas A&M University, College Station, TX, 77843-3255, USA.
Jean-Philippe PelloisDepartment of Chemistry, Texas A&M University, College Station, TX, 77843-3255, USA.
Hong-Cai ZhouDepartment of Chemistry, Texas A&M University, College Station, TX, 77843-3255, USA.ORCID 0000-0002-9029-3788
Texas A&M University · USChinese Academy of Sciences · CN

Funding

Mechanisms and optimization of endosomal escape for delivery applicationsR01GM110137 · NIGMS · TEXAS A&M AGRILIFE RESEARCH · PI PELLOIS, JEAN-PHILIPPE · 2015 to 2022
$2.3M
NIGMS NIH HHS R01 GM110137
6 · The paper itself

Abstract

Prodrug activation, by exogenously administered enzymes, for cancer therapy is an approach to achieve better selectivity and less systemic toxicity than conventional chemotherapy. However, the short half-lives of the activating enzymes in the bloodstream has limited its success. Demonstrated here is that a tyrosinase-MOF nanoreactor activates the prodrug paracetamol in cancer cells in a long-lasting manner. By generating reactive oxygen species (ROS) and depleting glutathione (GSH), the product of the enzymatic conversion of paracetamol is toxic to drug-resistant cancer cells. Tyrosinase-MOF nanoreactors cause significant cell death in the presence of paracetamol for up to three days after being internalized by cells, while free enzymes totally lose activity in a few hours. Thus, enzyme-MOF nanocomposites are envisioned to be novel persistent platforms for various biomedical applications.

Indexed as

AcetaminophenAntineoplastic AgentsCell Line, TumorCell ProliferationDose-Response Relationship, DrugDrug Screening Assays, AntitumorHeLa CellsHumansMetal-Organic FrameworksModels, MolecularMolecular StructureMonophenol MonooxygenaseNanoparticlesParticle SizeStructure-Activity RelationshipSurface PropertiesAcetaminophenAntineoplastic AgentsMetal-Organic FrameworksMonophenol Monooxygenasecancerdrug deliveryenzymesmetal-organic frameworksnanoparticles

Identifiers

PMID29536600
PMCPMC6621563
OpenAlexW2791332947

What OpenQuestion holds

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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.