Evidence map›Paper›PMID 42871768›Full record

ReviewGenes & diseases2027

Disulfidptosis-based cancer therapy: Opportunity and challenge.

Bo Wang, Zihui Liu, Junjie Li, Jiaxing Xu, Yamei Guo, Jingxue Zhang, Ti Chu, Zhifen Feng, Qiying Jiang, Dongdong Wu

Abstract readReview
In one paragraph

Review in Genes & diseases, 2027. 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

10 authors.

Bo WangDepartment of Stomatology, Huaihe Hospital of Henan University, School of Stomatology, Henan University, Kaifeng, Henan 475004, China.
Zihui LiuDepartment of Stomatology, Huaihe Hospital of Henan University, School of Stomatology, Henan University, Kaifeng, Henan 475004, China.
Junjie LiDepartment of Stomatology, Huaihe Hospital of Henan University, School of Stomatology, Henan University, Kaifeng, Henan 475004, China.
Jiaxing XuDepartment of Stomatology, Huaihe Hospital of Henan University, School of Stomatology, Henan University, Kaifeng, Henan 475004, China.
Yamei GuoDepartment of Stomatology, Huaihe Hospital of Henan University, School of Stomatology, Henan University, Kaifeng, Henan 475004, China.
Jingxue ZhangDepartment of Stomatology, Huaihe Hospital of Henan University, School of Stomatology, Henan University, Kaifeng, Henan 475004, China.
Ti ChuHenan International Joint Laboratory for Nuclear Protein Regulation, School of Basic Medical Sciences, School of Stomatology, Henan University, Kaifeng, Henan 475004, China.
Zhifen FengSchool of Nursing and Health, Henan University, Kaifeng, Henan 475004, China.
Qiying JiangHenan International Joint Laboratory for Nuclear Protein Regulation, School of Basic Medical Sciences, School of Stomatology, Henan University, Kaifeng, Henan 475004, China.
Dongdong WuDepartment of Stomatology, Huaihe Hospital of Henan University, School of Stomatology, Henan University, Kaifeng, Henan 475004, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer represents a significant global health threat, with traditional treatment modalities often facing substantial limitations. Consequently, novel therapeutic strategies have garnered considerable interest. In recent years, regulated cell death has achieved remarkable success in cancer treatment, as it is crucial for eliminating abnormal cells. Strategies aimed at inducing regulated cell death, especially disulfidptosis, have become increasingly important in cancer therapy. As a newly identified form of cell death, disulfidptosis has attracted growing attention in cancer research. This process is intricately linked to cystine uptake, consumption, and alterations in the actin cytoskeleton. In addition, disulfidptosis has been effectively utilized in bioinformatics research and has emerged as a biomarker for various cancer types, with the potential to serve as a therapeutic target. This review provides a comprehensive analysis of the canonical disulfidptosis signaling pathway, recent research advancements, and its application potential in oncology. We also examine current bioinformatics-derived biomarkers and potential targets. Crucially, we explore potential research directions for disulfidptosis in cancer and identify existing research challenges.

Indexed as

CancerDisulfidptosisNADPHRegulated cell death

Identifiers

PMID42871768
PMCPMC13659332

What OpenQuestion holds

Textmetadata
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.