Evidence map›Paper›PMID 36660553›Full record

ArticleAsian journal of pharmaceutical sciences2023

Reversing ferroptosis resistance by MOFs through regulation intracellular redox homeostasis.

Chengcheng Wang, Jiao Wang, Xue Pan, Shuang Yu, Meiqi Chen, Yan Gao, Zilin Song, Haiyang Hu, Xiuli Zhao, Dawei Chen and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Asian journal of pharmaceutical sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. HMGB1: a multifaceted mediator of cell death pathways in cardiovascular diseases.Apoptosis : an international journal on programmed cell death · 2025
    Review
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  6. Article
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  11. Metal-organic framework-modulated FeJournal of nanobiotechnology · 2023
    Article
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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

12 authors at 2 institutions in 1 country.

Chengcheng WangSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Jiao WangYantai Luyin Pharmaceutical Co. Ltd., Yantai 264002, China.
Xue PanQingdao Marine Biomedical Research Institute, Qingdao 266071, China.
Shuang YuSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Meiqi ChenSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Yan GaoSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Zilin SongSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Haiyang HuSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Xiuli ZhaoSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Dawei ChenSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Fei HanSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Mingxi QiaoSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Shenyang Pharmaceutical University · CNMarine Biomedical Research Institute of Qingdao · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As a non-apoptotic cell death form, ferroptosis offers an alternative approach to overcome cancer chemotherapy resistance. However, accumulating evidence indicates cancer cells can develop ferroptosis resistance by evolving antioxidative defense mechanisms. To address this issue, we prepared a Buthionine-(S,R)-sulfoximine (BSO) loaded metal organic framework (MOF) of BSO-MOF-HA (BMH) with the combination effect of boosting oxidative damage and inhibiting antioxidative defense. MOF nanoparticle was constructed by the photosensitizer of [4,4,4,4-(porphine-5,10,15,20-tetrayl) tetrakis (benzoic acid)] (TCPP) and the metal ion of Zr6, which was further decorated with hyaluronic acid (HA) in order to impart active targeting to CD44 receptors overexpressed cancer cells. BMH exhibited a negative charge and spherical shape with average particle size about 162.5 nm. BMH was found to restore the susceptibility of 4T1 cells to ferroptosis under irradiation. This was attributed to the combination of photodynamic therapy (PDT) and γ-glutamylcysteine synthetase inhibitor of BSO, shifting the redox balance to oxidative stress. Enhanced ferroptosis also induced the release of damage associated molecular patterns (DAMPs) to maturate dendritic cells and activated T lymphocytes, leading to superior anti-tumor performance

Indexed as

Buthionine-(S,R)-sulfoximineFerroptosisGlutathioneImmunogenic cell deathMetal organic frameworkPhotodynamic therapy

Identifiers

PMID36660553
PMCPMC9841358
OpenAlexW4311989049

What OpenQuestion 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 OpenQuestion graph.