Evidence map›Paper›PMID 39477929›Full record

ArticleNature communications2024

Tumor-targeted glutathione oxidation catalysis with ruthenium nanoreactors against hypoxic osteosarcoma.

Hanchen Zhang, Nicolás Montesdeoca, Dongsheng Tang, Ganghao Liang, Minhui Cui, Chun Xu, Lisa-Marie Servos, Tiejun Bing, Zisis Papadopoulos, Meifang Shen and 3 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

26 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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.

Hanchen ZhangBeijing National Laboratory for Molecular Sciences, Laboratory of Polymer Physics and Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China.
Nicolás MontesdeocaFaculty of Chemistry and Biochemistry, Ruhr-University Bochum, Bochum, Germany.
Dongsheng TangBeijing National Laboratory for Molecular Sciences, Laboratory of Polymer Physics and Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China.
Ganghao LiangBeijing National Laboratory for Molecular Sciences, Laboratory of Polymer Physics and Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China.
Minhui CuiBeijing National Laboratory for Molecular Sciences, Laboratory of Polymer Physics and Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China.
Chun XuSchool of Dentistry, The University of Queensland, Brisbane, QLD, Australia.ORCID 0000-0001-8831-3607
Lisa-Marie ServosFaculty of Chemistry and Biochemistry, Ruhr-University Bochum, Bochum, Germany.
Tiejun BingImmunology and Oncology center, ICE Bioscience, Beijing, China.
Zisis PapadopoulosFaculty of Chemistry and Biochemistry, Ruhr-University Bochum, Bochum, Germany.
Meifang ShenState Key Laboratory of Organic-Inorganic Composites, Beijing Laboratory of Biomedical Materials, Beijing University of Chemical Technology, Beijing, China.
Haihua XiaoBeijing National Laboratory for Molecular Sciences, Laboratory of Polymer Physics and Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China. hhxiao@iccas.ac.cn.ORCID 0000-0001-8159-8187
Yingjie YuState Key Laboratory of Organic-Inorganic Composites, Beijing Laboratory of Biomedical Materials, Beijing University of Chemical Technology, Beijing, China. yuyingjie@mail.buct.edu.cn.ORCID 0000-0002-2543-9808
Johannes KargesFaculty of Chemistry and Biochemistry, Ruhr-University Bochum, Bochum, Germany. johannes.karges@ruhr-uni-bochum.de.ORCID 0000-0001-5258-0260

Funding

National Natural Science Foundation of China (National Science Foundation of China) 22175189; 52373127Natural Science Foundation of Beijing Municipality (Beijing Natural Science Foundation) JQ24055
6 · The paper itself

Abstract

The majority of anticancer agents have a reduced or even complete loss of a therapeutic effect within hypoxic tumors. To overcome this limitation, research efforts have been devoted to the development of therapeutic agents with biological mechanisms of action that are independent of the oxygen concentration. Here we show the design, synthesis, and biological evaluation of the incorporation of a ruthenium (Ru) catalyst into polymeric nanoreactors for hypoxic anticancer therapy. The nanoreactors can catalyze the oxidation of glutathione (GSH) to glutathione disulfide (GSSG) in hypoxic cancer cells. This initiates the buildup of reactive oxygen species (ROS) and lipid peroxides, leading to the demise of cancer cells. It also stimulates the overexpression of the transient receptor potential melastatin 2 (TRPM2) ion channels, triggering macrophage activation, leading to a systemic immune response. Upon intravenous injection, the nanoreactors can systemically activate the immune system, and nearly fully eradicate an aggressive osteosarcoma tumor inside a mouse model.

Indexed as

GlutathioneOsteosarcomaOxidation-ReductionReactive Oxygen SpeciesRutheniumAnimalsAntineoplastic AgentsBone NeoplasmsCatalysisCell Line, TumorFemaleHumansMiceTRPM Cation ChannelsXenograft Model Antitumor AssaysAntineoplastic AgentsGlutathioneReactive Oxygen SpeciesRutheniumTRPM Cation Channels

Identifiers

PMID39477929
PMCPMC11526146

What OpenQuestion holds

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Registered trials

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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.