Evidence map›Paper›PMID 41869756›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Biomimetic Nanoplatform for Targeted Glioblastoma Therapy via Concurrently Triggering GPX4/DHODH Mediated Ferroptosis.

Guodong Ren, Xuewei Wang, Panpan Li, Hao Wu, Zhifei Bi, Qi Gao, Bolong Ma, Zixuan Tian, Jianfei Liu, Fuqiang Feng and 3 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Guodong RenSchool of Basic Medical Sciences, Shanxi Medical University, Taiyuan, China.
Xuewei WangSchool of Basic Medical Sciences, Shanxi Medical University, Taiyuan, China.
Panpan LiState Key Laboratory of Flexible Electronics (LoFE) & Institute of Flexible Electronics (IFE), Northwestern Polytechnical University, Xi'an, China.
Hao WuSchool of Basic Medical Sciences, Shanxi Medical University, Taiyuan, China.
Zhifei BiSchool of Basic Medical Sciences, Shanxi Medical University, Taiyuan, China.
Qi GaoSchool of Basic Medical Sciences, Shanxi Medical University, Taiyuan, China.
Bolong MaSchool of Basic Medical Sciences, Shanxi Medical University, Taiyuan, China.
Zixuan TianSchool of Basic Medical Sciences, Shanxi Medical University, Taiyuan, China.
Jianfei LiuSchool of Basic Medical Sciences, Shanxi Medical University, Taiyuan, China.
Fuqiang FengDepartment of Neurosurgery, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, China.
Wen LiuSchool of Basic Medical Sciences, Shanxi Medical University, Taiyuan, China.
Lin LiState Key Laboratory of Flexible Electronics (LoFE) & Institute of Flexible Electronics (IFE), Northwestern Polytechnical University, Xi'an, China.ORCID https://orcid.org/0000-0003-0426-6546
Chengwu ZhangSchool of Basic Medical Sciences, Shanxi Medical University, Taiyuan, China.

Funding

Basic Research Plan Project of Shanxi Province 20210302123265Fujian Provincial Natural Science Foundation of China 2024J01060Ministry of Education of China JYB2025XDXM406National Natural Science Foundation of China 22577108Research Fund of Shanxi Province Health Commission 2021060Shanxi Basic Research Program for Young Scientists 202203021212366
6 · The paper itself

Abstract

Glioblastoma multiforme (GBM), the most aggressive and lethal type of brain cancer, is a considerable threat to human health. Conventional therapeutic modalities fail to yield satisfactory outcomes; therefore, a more effective intervention strategy is urgently required. Ferroptosis, a novel type of cell death, has potential for GBM therapy. However, its efficacy is substantially compromised by the tumor-intrinsic anti-ferroptosis defense system. Moreover, approaches that trigger ferroptosis by modulating a single target are insufficient. Thus, it is imperative to simultaneously inhibit anti-ferroptotic regulators to overcome compensatory pathways and achieve robust tumor eradication. Therefore, in the present study, a multifunctional nanoplatform, hollow mesoporous manganese dioxide (H-MnO

Indexed as

BiomimeticsBrain NeoplasmsFerroptosisGlioblastomaPhospholipid Hydroperoxide Glutathione PeroxidaseAnimalsBiomimetic MaterialsCell Line, TumorHumansManganese CompoundsMiceOxidesManganese Compoundsmanganese dioxideOxidesPhospholipid Hydroperoxide Glutathione PeroxidaseDHODHferroptosisglioblastomaGPX4H‐MnO2

Identifiers

PMID41869756
PMCPMC13587953

What OpenQuestion holds

Textmetadata
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.