Evidence map›Paper›PMID 41449419›Full record

ReviewJournal of nanobiotechnology2025

2D nanomaterial-triggered ferroptosis in cancer therapy.

Yue Gao, Jiahao Xu, Yuanqiu Lai, Yaoxuan Fan, Yuhan Zhou, Ying Tu, Xiang Liu, Xueqian Xia, Gui-Na Wei, Jia-Wei Shen and 1 more

Abstract readReview
In one paragraph

Review in Journal of nanobiotechnology, 2025. 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

11 authors.

Yue GaoZhejiang Provincial Key Laboratory of Anti-Cancer Chinese Medicines and Natural Medicines, School of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Jiahao XuZhejiang Provincial Key Laboratory of Anti-Cancer Chinese Medicines and Natural Medicines, School of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Yuanqiu LaiZhejiang Provincial Key Laboratory of Anti-Cancer Chinese Medicines and Natural Medicines, School of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Yaoxuan FanZhejiang Provincial Key Laboratory of Anti-Cancer Chinese Medicines and Natural Medicines, School of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Yuhan ZhouZhejiang Provincial Key Laboratory of Anti-Cancer Chinese Medicines and Natural Medicines, School of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Ying TuZhejiang Provincial Key Laboratory of Anti-Cancer Chinese Medicines and Natural Medicines, School of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Xiang LiuZhejiang Provincial Key Laboratory of Anti-Cancer Chinese Medicines and Natural Medicines, School of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Xueqian XiaZhejiang Provincial Key Laboratory of Anti-Cancer Chinese Medicines and Natural Medicines, School of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Gui-Na WeiDepartment of Nephrology, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China. weiguina@163.com.
Jia-Wei ShenZhejiang Provincial Key Laboratory of Anti-Cancer Chinese Medicines and Natural Medicines, School of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China. shen.jiawei@hotmail.com.
Wei DuanZhejiang Provincial Key Laboratory of Anti-Cancer Chinese Medicines and Natural Medicines, School of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China. duanweichem@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer therapy faces significant challenges due to the resistance of traditional apoptosis-based treatments. Ferroptosis, an iron-dependent, lipid peroxidation-driven form of programmed cell death, has emerged as a novel therapeutic strategy owing to its unique metabolic regulation mechanisms. However, conventional small-molecule ferroptosis inducers suffer from poor targeting and rapid metabolism. The integration of nanotechnology provides innovative solutions for precise ferroptosis modulation. Among various nanomaterials, two-dimensional (2D) nanomaterials stand out due to their distinctive physicochemical properties and multifunctionality, making them widely studied in ferroptosis-mediated cancer therapy. In this review, we first outline the development, physiological mechanisms, detection markers, and common methodologies of ferroptosis, while highlighting the current challenges in ferroptosis-related cancer therapies. Second, we discuss the general principles of 2D materials in inducing ferroptosis, emphasizing how these platforms enhance ferroptosis efficacy. Third, we classify and elaborate on different types of 2D materials that induce ferroptosis in tumor cells. Finally, we present future perspectives in this field. We hope this review will facilitate the rational design of 2D materials for ferroptosis induction and pave the way for broader biomedical applications.

Indexed as

Antineoplastic AgentsFerroptosisNanostructuresNeoplasmsAnimalsHumansIronLipid PeroxidationAntineoplastic AgentsIronFerroptosisReactive oxygen speciesSynergistic tumor therapyTargeted deliveryTwo-dimensional nanomaterials

Identifiers

PMID41449419
PMCPMC12849271

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.