Evidence map›Paper›PMID 39120559›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Cholesterol Depletion-Enhanced Ferroptosis and Immunotherapy via Engineered Nanozyme.

Tingjie Bai, Panpan Xue, Sijie Shao, Shuangqian Yan, Xuemei Zeng

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. 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
–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

30 citing papers in PubMed.

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  16. Inducing ferroptosis to improve cancer therapy: a promising tool for enhancing immunotherapy.Journal of experimental & clinical cancer research : CR · 2025
    Review
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  18. 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

5 authors.

Tingjie BaiKey Laboratory of Microbial Pathogenesis and Interventions of Fujian Province University, Biomedical Research Center of South China, College of Life Sciences, Fujian Normal University, Fuzhou, 350117, China.
Panpan XueThe Straits Institute of Flexible Electronics (SIFE, Future Technologies), Straits Laboratory of Flexible Electronics (SLoFE), Fujian Normal University, Fuzhou, 350117, China.
Sijie ShaoThe Straits Institute of Flexible Electronics (SIFE, Future Technologies), Straits Laboratory of Flexible Electronics (SLoFE), Fujian Normal University, Fuzhou, 350117, China.
Shuangqian YanThe Straits Institute of Flexible Electronics (SIFE, Future Technologies), Straits Laboratory of Flexible Electronics (SLoFE), Fujian Normal University, Fuzhou, 350117, China.
Xuemei ZengKey Laboratory of Microbial Pathogenesis and Interventions of Fujian Province University, Biomedical Research Center of South China, College of Life Sciences, Fujian Normal University, Fuzhou, 350117, China.ORCID 0009-0004-6853-6343

Funding

National Natural Science Foundation of China 32201153National Natural Science Foundation of China 62275048Science and Technology Planning Project of Fujian Province 2021J05031Science and Technology Planning Project of Fujian Province 2023J01292
6 · The paper itself

Abstract

Ferroptosis, an iron- and reactive oxygen species (ROS)-dependent cell death, holds significant promise for tumor therapy due to its ability to induce lipid peroxidation (LPO) and trigger antitumor immune responses. However, elevated cholesterol levels in cancer cells impede ferroptosis and compromise immune function. Here, a novel nanozyme, Fe-MOF/CP, composed of iron metal-organic framework (Fe-MOF) nanoparticles loaded with cholesterol oxidase and PEGylation for integrated ferroptosis and immunotherapy is introduced. Fe-MOF/CP depletes cholesterol and generates hydrogen peroxide, enhancing ROS levels and inducing LPO, thereby promoting ferroptosis. This process disrupts lipid raft integrity and downregulates glutathione peroxidase 4 and ferroptosis suppressor protein 1, further facilitating ferroptosis. Concurrently, Fe-MOF/CP augments immunogenic cell death, reduces programmed death-ligand 1 expression, and revitalizes exhausted CD8

Indexed as

CholesterolDisease Models, AnimalFerroptosisImmunotherapyAnimalsCell Line, TumorHumansMetal-Organic FrameworksMiceMice, Inbred C57BLNanoparticlesNeoplasmsReactive Oxygen SpeciesCholesterolMetal-Organic FrameworksReactive Oxygen Speciescholesterol metabolismferroptosisimmunotherapynanozyme

Identifiers

PMID39120559
PMCPMC11481222

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.