Evidence map›Paper›PMID 38994406›Full record

ArticleChemical science2024

How does ferrocene correlate with ferroptosis? Multiple approaches to explore ferrocene-appended GPX4 inhibitors as anticancer agents.

Wei Li, Jing Yu, Jing Wang, Xuejing Fan, Ximing Xu, Hui Wang, Ying Xiong, Xinyu Li, Xiaomin Zhang, Qianer Zhang and 10 more

Abstract read
In one paragraph

Article in Chemical science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Chemo-photothermal synergy ignites antitumor immunity via ferroptosis.Signal transduction and targeted therapy · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
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

20 authors.

Wei LiSchool of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Chinese Ministry of Education, Ocean University of China Qingdao 26003 Shandong P. R. China lijing_ouc@ouc.edu.cn wangyong8866@ouc.edu.cn.
Jing YuSchool of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Chinese Ministry of Education, Ocean University of China Qingdao 26003 Shandong P. R. China lijing_ouc@ouc.edu.cn wangyong8866@ouc.edu.cn.
Jing WangSchool of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Chinese Ministry of Education, Ocean University of China Qingdao 26003 Shandong P. R. China lijing_ouc@ouc.edu.cn wangyong8866@ouc.edu.cn.
Xuejing FanSchool of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Chinese Ministry of Education, Ocean University of China Qingdao 26003 Shandong P. R. China lijing_ouc@ouc.edu.cn wangyong8866@ouc.edu.cn.
Ximing XuMarine Biomedical Research Institute of Qingdao, School of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Chinese Ministry of Education, Ocean University of China Qingdao 266003 Shandong P. R. China.ORCID https://orcid.org/0000-0002-2125-7345
Hui WangSchool of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Chinese Ministry of Education, Ocean University of China Qingdao 26003 Shandong P. R. China lijing_ouc@ouc.edu.cn wangyong8866@ouc.edu.cn.
Ying XiongSchool of Pharmacy, Fudan University Shanghai 201203 China.
Xinyu LiSchool of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Chinese Ministry of Education, Ocean University of China Qingdao 26003 Shandong P. R. China lijing_ouc@ouc.edu.cn wangyong8866@ouc.edu.cn.
Xiaomin ZhangSchool of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Chinese Ministry of Education, Ocean University of China Qingdao 26003 Shandong P. R. China lijing_ouc@ouc.edu.cn wangyong8866@ouc.edu.cn.
Qianer ZhangSchool of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Chinese Ministry of Education, Ocean University of China Qingdao 26003 Shandong P. R. China lijing_ouc@ouc.edu.cn wangyong8866@ouc.edu.cn.
Xin QiSchool of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Chinese Ministry of Education, Ocean University of China Qingdao 26003 Shandong P. R. China lijing_ouc@ouc.edu.cn wangyong8866@ouc.edu.cn.
Pascal PigeonPSL, Chimie ParisTech 11 Rue Pierre et Marie Curie F-75005 Paris France.
Qing GuState Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences 345 Lingling Lu Shanghai 200032 P. R. China.
Julia Bruno-ColmenarezUCD School of Chemistry, University College Dublin Belfield Dublin 4 Ireland.ORCID https://orcid.org/0000-0001-9476-7189
Gérard JaouenPSL, Chimie ParisTech 11 Rue Pierre et Marie Curie F-75005 Paris France.
Michael J McGlincheyUCD School of Chemistry, University College Dublin Belfield Dublin 4 Ireland.
Xue QiuSchool of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Chinese Ministry of Education, Ocean University of China Qingdao 26003 Shandong P. R. China lijing_ouc@ouc.edu.cn wangyong8866@ouc.edu.cn.
Shu-Li YouState Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences 345 Lingling Lu Shanghai 200032 P. R. China.ORCID https://orcid.org/0000-0003-4586-8359
Jing LiSchool of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Chinese Ministry of Education, Ocean University of China Qingdao 26003 Shandong P. R. China lijing_ouc@ouc.edu.cn wangyong8866@ouc.edu.cn.
Yong WangSchool of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Chinese Ministry of Education, Ocean University of China Qingdao 26003 Shandong P. R. China lijing_ouc@ouc.edu.cn wangyong8866@ouc.edu.cn.ORCID https://orcid.org/0000-0003-3222-0211

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ferroptosis has emerged as a form of programmed cell death and exhibits remarkable promise for anticancer therapy. However, it is challenging to discover ferroptosis inducers with new chemotypes and high ferroptosis-inducing potency. Herein, we report a new series of ferrocenyl-appended GPX4 inhibitors rationally designed in a "one stone kills two birds" strategy. Ferroptosis selectivity assays, GPX4 inhibitory activity and CETSA experiments validated the inhibition of novel compounds on GPX4. In particular, the ROS-related bioactivity assays highlighted the ROS-inducing ability of 17 at the molecular level and their ferroptosis enhancement at the cellular level. These data confirmed the dual role of ferrocene as both the bioisostere motif maintaining the inhibition capacity of certain molecules with GPX4 and also as the ROS producer to enhance the vulnerability to ferroptosis of cancer cells, thereby attenuating tumor growth

Identifiers

PMID38994406
PMCPMC11234876

What OpenQuestion holds

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Registered trials

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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.