Evidence map›Paper›PMID 35023280›Full record

ArticleJournal of cellular and molecular medicine2022

Ferroptosis-related gene NOX4, CHAC1 and HIF1A are valid biomarkers for stomach adenocarcinoma.

Ruoxi Xiao, Shasha Wang, Jing Guo, Shihai Liu, Aiping Ding, Gongjun Wang, Wenqian Li, Yuqi Zhang, Xiaoqian Bian, Shufen Zhao and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
12.6field-weighted citation impact, top 1% 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

40 citing papers in PubMed, 80 citations in OpenAlex.

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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

11 authors at 1 institution in 1 country.

Ruoxi XiaoDepartment of Medcine, Qingdao University, Qingdao, China.ORCID 0000-0002-0801-7005
Shasha WangDepartment of Oncology, Affiliated Hospital of Qingdao University, Qingdao, China.
Jing GuoDepartment of Oncology, Affiliated Hospital of Qingdao University, Qingdao, China.
Shihai LiuDepartment of Oncology, Affiliated Hospital of Qingdao University, Qingdao, China.
Aiping DingDepartment of Oncology, Affiliated Hospital of Qingdao University, Qingdao, China.
Gongjun WangDepartment of Medcine, Qingdao University, Qingdao, China.
Wenqian LiDepartment of Medcine, Qingdao University, Qingdao, China.
Yuqi ZhangDepartment of Medcine, Qingdao University, Qingdao, China.
Xiaoqian BianDepartment of Medcine, Qingdao University, Qingdao, China.
Shufen ZhaoDepartment of Oncology, Affiliated Hospital of Qingdao University, Qingdao, China.
Wensheng QiuDepartment of Oncology, Affiliated Hospital of Qingdao University, Qingdao, China.ORCID 0000-0002-4293-9193
Qingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ferroptosis is a regulated cell death nexus linking metabolism, redox biology and diseases including cancer. The aim of the present study was to identify a ferroptosis-related gene prognostic signature for stomach adenocarcinoma (STAD) by systematic analysis of transcriptional profiles from The Cancer Genome Atlas (TCGA), GEO and a clinical cohort from our centre. We developed a predictive model based on three ferroptosis-related genes (CHAC1, NOX4 and HIF1A), gene expression data and corresponding clinical outcomes were obtained from the TCGA database, and the reliability of this model was verified with GSE15459 and 51 queues in our centre. ROC curve showed better predictive ability using the risk score. Immune cell enrichment analysis demonstrated that the types of immune cells and their expression levels in the high-risk group were significantly different from those in the low-risk group. The experimental results confirmed that NOX4 was upregulated and CHAC1 was downregulated in the STAD tissues compared with the normal stomach mucosal tissues (p < 0.05). In sum, the ferroptosis-related gene signature can accurately predict the outcomes of patients with STAD, providing valuable insights for personalized treatment. As the signature also has relevance to the immune characteristics, it may help improve the efficacy of personalized immunotherapy.

Indexed as

AdenocarcinomaFerroptosisBiomarkers, TumorGene Expression ProfilingGene Expression Regulation, NeoplasticHumansHypoxia-Inducible Factor 1, alpha SubunitNADPH Oxidase 4Reproducibility of ResultsStomachBiomarkers, TumorHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitNADPH Oxidase 4NOX4 protein, humanCHAC1ferroptosisHIF1ANOX4prognostic signaturestomach adenocarcinoma

Identifiers

PMID35023280
PMCPMC8831942
OpenAlexW4206068704

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.