Evidence map›Paper›PMID 38476278›Full record

ReviewInternational journal of nanomedicine2024

Advances in Ferroptosis-Inducing Agents by Targeted Delivery System in Cancer Therapy.

Debiao Xiang, Lili Zhou, Rui Yang, Fang Yuan, Yilin Xu, Yuan Yang, Yong Qiao, Xin Li

Open access · goldAbstract readReview
In one paragraph

Review in International journal of nanomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  7. Programmed cell death in triple-negative breast cancer.Cellular & molecular biology letters · 2025
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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

8 authors at 2 institutions in 1 country.

Debiao XiangDepartment of Pharmacy, The Third Hospital of Changsha, Changsha, Hunan Province, People's Republic of China.
Lili ZhouCollege of Pharmacy, Hunan University of Chinese Medicine, Changsha, Hunan Province, People's Republic of China.
Rui YangDepartment of Pharmacy, The Third Hospital of Changsha, Changsha, Hunan Province, People's Republic of China.
Fang YuanDepartment of Pharmacy, The Third Hospital of Changsha, Changsha, Hunan Province, People's Republic of China.
Yilin XuCollege of Pharmacy, Hunan University of Chinese Medicine, Changsha, Hunan Province, People's Republic of China.
Yuan YangDepartment of Pharmacy, The Third Hospital of Changsha, Changsha, Hunan Province, People's Republic of China.ORCID 0009-0002-8811-9841
Yong QiaoDepartment of Pharmacy, The Third Hospital of Changsha, Changsha, Hunan Province, People's Republic of China.
Xin LiDepartment of Pharmacy, The Third Hospital of Changsha, Changsha, Hunan Province, People's Republic of China.ORCID 0000-0002-8866-6848
Changsha University · CNHunan University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently, cancer remains one of the most significant threats to human health. Treatment of most cancers remains challenging, despite the implementation of diverse therapies in clinical practice. In recent years, research on the mechanism of ferroptosis has presented novel perspectives for cancer treatment. Ferroptosis is a regulated cell death process caused by lipid peroxidation of membrane unsaturated fatty acids catalyzed by iron ions. The rapid development of bio-nanotechnology has generated considerable interest in exploiting iron-induced cell death as a new therapeutic target against cancer. This article provides a comprehensive overview of recent advancements at the intersection of iron-induced cell death and bionanotechnology. In this respect, the mechanism of iron-induced cell death and its relation to cancer are summarized. Furthermore, the feasibility of a nano-drug delivery system based on iron-induced cell death for cancer treatment is introduced and analyzed. Secondly, strategies for inducing iron-induced cell death using nanodrug delivery technology are discussed, including promoting Fenton reactions, inhibiting glutathione peroxidase 4, reducing low glutathione levels, and inhibiting system Xc

Indexed as

FerroptosisNeoplasmsCell DeathCombined Modality TherapyHumansIronLipid PeroxidationIroncancersferroptosisnano-drug delivery systemtarget

Identifiers

PMID38476278
PMCPMC10929151
OpenAlexW4392377742

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.