Evidence map›Paper›PMID 39501397›Full record

ArticleHuman genomics2024

Development of oxidative stress- and ferroptosis-related prognostic signature in gastric cancer and identification of CDH19 as a novel biomarker.

Shibo Wang, Siyi Zhang, Xiaoxuan Li, Chuanyu Leng, Xiangxue Li, Jing Lv, Shufen Zhao, Wensheng Qiu, Jing Guo

Abstract read
In one paragraph

Article in Human genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Targeting ferroptosis inInternational journal of oncology · 2026
    Review
  6. Article
  7. 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

9 authors.

Shibo Wang *Department of Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong Province, 266000, China.
Siyi Zhang *Department of Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong Province, 266000, China.
Xiaoxuan LiDepartment of Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong Province, 266000, China.
Chuanyu LengDepartment of Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong Province, 266000, China.
Xiangxue LiDepartment of Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong Province, 266000, China.
Jing LvDepartment of Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong Province, 266000, China.
Shufen ZhaoDepartment of Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong Province, 266000, China.
Wensheng QiuDepartment of Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong Province, 266000, China. wsqiuqdfy@qdu.edu.cn.
Jing GuoDepartment of Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong Province, 266000, China. guojing-melody@163.com.

Funding

Beijing Xisike Clinical Oncology Research Foundation No.Y2019-AZZD-0471Qingdao Key Clinical Specialty Elite Discipline No.Y-HR2018-185
6 · The paper itself

Abstract

backgroundFerroptosis is a unique mode of cell death that is iron-dependent and associated with oxidative stress and lipid peroxidation. Oxidative stress and ferroptosis are essential mechanisms leading to metabolic abnormalities in cells and have been popular areas in cancer research.

methodsInitially, 76 oxidative stress and ferroptosis-related genes (OFRGs) were acquired by intersecting the gene sets from oxidative stress and ferroptosis. Afterwards, optimal OFRGs were screened using PPI networks, and individuals were separated into two OFRG subtypes (K = 2). Subsequently, we successfully constructed and verified a prognostic signature comprising SLC7A2, Cadherin 19 (CDH19), and CCN1. To further uncover potential biomarkers of gastric cancer (GC), we examined the expression level of CDH19, investigated the effects of knocking down CDH19 on the biological behavior of GC cells, and explored whether CDH19 is involved in ferroptosis and oxidative stress processes.

resultsAccording to the findings, individuals in the low-risk scoring group have less infiltration of immune suppressive cells, fewer occurrences of immune escape and dysfunction, greater efficacy in chemotherapy and immunotherapy, and better survival outcomes. The qRT-PCR assay indicated that CDH19 expression was significantly higher in GC cells. Through experiments, we demonstrated that knocking down CDH19 can affect the transcription levels of ACSL4 and GPX4, increase intracellular iron ion concentration and accumulation of reactive oxygen species (ROS), and inhibit the proliferation and migration of GC cells.

conclusionWe developed an OFRG-related signature to predict the prognosis and treatment responsiveness of individuals with GC and identified CDH19 as a possible therapeutic target for GC.

Indexed as

Biomarkers, TumorCadherinsFerroptosisGene Expression Regulation, NeoplasticOxidative StressStomach NeoplasmsCell Line, TumorCell ProliferationFemaleHumansPrognosisBiomarkers, TumorCadherinsCDH19Immunotherapy ferroptosisOxidative stressPrognostic biomarker

Identifiers

PMID39501397
PMCPMC11536560

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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.