Evidence map›Paper›PMID 37370105›Full record

ArticleJournal of nanobiotechnology2023

Anti-Her2 affibody-decorated arsenene nanosheets induce ferroptosis through depleting intracellular GSH to overcome cisplatin resistance.

Peng He, Shenglin Xu, Zhaohua Miao, Yukang Que, Yu Chen, Sheng Li, Qiming Ma, Rui Yang, Wei Wei, Zhengbao Zha and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

12 citing papers in PubMed, 26 citations in OpenAlex.

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  8. Single-Cell Spatial-Temporal Analysis ofResearch (Washington, D.C.) · 2024
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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

11 authors at 4 institutions in 1 country.

Peng He *Department of Orthopedics, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, Anhui, China.
Shenglin Xu *Department of Orthopedics, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, Anhui, China.
Zhaohua MiaoSchool of Food and Biological Engineering, Hefei University of Technology, Hefei, 230009, Anhui, China.
Yukang QueDepartment of Orthopedics, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, Anhui, China.
Yu ChenDepartment of Pharmacy, Anqing Medical College, Anqing, 246052, Anhui, China.
Sheng LiDepartment of Orthopedics, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, Anhui, China.
Qiming MaDepartment of Orthopedics, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, Anhui, China.
Rui YangDepartment of Orthopedics, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, Anhui, China.
Wei WeiInstitute of Clinical Pharmacology, Anhui Medical University, Hefei, 230032, Anhui, China. wwei@ahmu.edu.cn.
Zhengbao ZhaSchool of Food and Biological Engineering, Hefei University of Technology, Hefei, 230009, Anhui, China. zbzha@hfut.edu.cn.
Yong HuDepartment of Orthopedics, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, Anhui, China. hy.in163@163.com.
Anhui Medical University · CNFirst Affiliated Hospital of Anhui Medical University · CNHefei University of Technology · CNAnqing Normal University · CN

Funding

The Basic and Clinical Cooperative Research Project of Anhui Medical University 2020xkjT033The Major Project of Natural Science Foundation of Anhui Province Colleges and Universities KJ2020ZD17The Open Fund Project of the Key Laboratory of Anti-inflammatory and Immunological Drugs of the Ministry of Education KFJJ-2020-04
6 · The paper itself

Abstract

Ferroptosis, a form of regulated cell death induced by excessive accumulation of reactive oxygen species and lipid peroxidation, has recently attracted extensive attention due to its ability to effectively suppress tumors and overcome drug resistance. Unlike previously reported metal nanomaterials that induce ferroptosis via the Fenton reaction, arsenene nanosheets can effectively deplete intracellular glutathione and then induce ferroptosis by inhibiting glutathione peroxidase 4. In this study, we designed target-modified arsenene nanosheets loaded with cisplatin (Her2-ANs@CDDP), which are capable of selective uptake by tumor cells. Her2-ANs@CDDP promotes both apoptosis and ferroptosis through a reciprocal cascade reaction between cisplatin and the carrier, respectively, and we demonstrate that it can significantly inhibit the activity of drug-resistant cells. Arsenene nanosheets kill drug-resistant tumor cells by inducing ferroptosis and restoring the sensitivity of drug-resistant cells to cisplatin. Cisplatin-loaded arsenene nanosheets can be prepared simply, and exert synergistic effects that overcome drug resistance. They show great potential for applications in the clinical treatment of chemotherapy-insensitive osteosarcoma, expanding the uses of arsenic in the treatment of solid tumors.

Indexed as

Antineoplastic AgentsBone NeoplasmsFerroptosisOsteosarcomaCell Line, TumorCisplatinGlutathioneHumansReactive Oxygen SpeciesAntineoplastic AgentsCisplatinGlutathioneReactive Oxygen SpeciesArsenene nanosheetsChemotherapyCisplatin resistanceFerroptosisOsteosarcoma

Identifiers

PMID37370105
PMCPMC10294336
OpenAlexW4382239715

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.