Evidence map›Paper›PMID 39379969›Full record

ReviewJournal of nanobiotechnology2024

Nanobiotechnology boosts ferroptosis: opportunities and challenges.

Shiqi Han, Jianhua Zou, Fan Xiao, Jing Xian, Ziwei Liu, Meng Li, Wei Luo, Chan Feng, Na Kong

Abstract readReview
In one paragraph

Review in Journal of nanobiotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

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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

9 authors.

Shiqi HanCollege of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Jianhua ZouLiangzhu Laboratory, Zhejiang University, Hangzhou, 311121, Zhejiang, China.
Fan XiaoLiangzhu Laboratory, Zhejiang University, Hangzhou, 311121, Zhejiang, China.
Jing XianCollege of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Ziwei LiuLiangzhu Laboratory, Zhejiang University, Hangzhou, 311121, Zhejiang, China.
Meng LiCollege of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Wei LuoCollege of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Chan FengLiangzhu Laboratory, Zhejiang University, Hangzhou, 311121, Zhejiang, China. chanfeng@zju.edu.cn.
Na KongLiangzhu Laboratory, Zhejiang University, Hangzhou, 311121, Zhejiang, China. kongna@zju.edu.cn.

Funding

China Postdoctoral Science Foundation 2023M733022National Natural Science Foundation of China 32201137National Natural Science Foundation of China 82122076Postdoctoral Fellowship Program of CPSF GZB20230652Youth Innovation Program of Zhejiang Provincial Medical and Health Science and Technology Plan 2023578116
6 · The paper itself

Abstract

Ferroptosis, distinct from apoptosis, necrosis, and autophagy, is a unique type of cell death driven by iron-dependent phospholipid peroxidation. Since ferroptosis was defined in 2012, it has received widespread attention from researchers worldwide. From a biochemical perspective, the regulation of ferroptosis is strongly associated with cellular metabolism, primarily including iron metabolism, lipid metabolism, and redox metabolism. The distinctive regulatory mechanism of ferroptosis holds great potential for overcoming drug resistance-a major challenge in treating cancer. The considerable role of nanobiotechnology in disease treatment has been widely reported, but further and more systematic discussion on how nanobiotechnology enhances the therapeutic efficacy on ferroptosis-associated diseases still needs to be improved. Moreover, while the exciting therapeutic potential of ferroptosis in cancer has been relatively well summarized, its applications in other diseases, such as neurodegenerative diseases, cardiovascular and cerebrovascular diseases, and kidney disease, remain underreported. Consequently, it is necessary to fill these gaps to further complete the applications of nanobiotechnology in ferroptosis. In this review, we provide an extensive introduction to the background of ferroptosis and elaborate its regulatory network. Subsequently, we discuss the various advantages of combining nanobiotechnology with ferroptosis to enhance therapeutic efficacy and reduce the side effects of ferroptosis-associated diseases. Finally, we analyze and discuss the feasibility of nanobiotechnology and ferroptosis in improving clinical treatment outcomes based on clinical needs, as well as the current limitations and future directions of nanobiotechnology in the applications of ferroptosis, which will not only provide significant guidance for the clinical applications of ferroptosis and nanobiotechnology but also accelerate their clinical translations.

Indexed as

FerroptosisNanotechnologyNeoplasmsAnimalsBiotechnologyHumansIronNeurodegenerative DiseasesIronClinical treatmentDrug deliveryDrug resistanceFerroptosisNanobiotechnologyRegulatory mechanism

Identifiers

PMID39379969
PMCPMC11460037

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.