Evidence map›Paper›PMID 35774297›Full record

ArticleComputational and mathematical methods in medicine2022

Prediction of Prognosis and Molecular Mechanism of Ferroptosis in Hepatocellular Carcinoma Based on Bioinformatics Methods.

Yuanpeng Xiong, Yonghao Ouyang, Kang Fang, Gen Sun, Shuju Tu, Wanpeng Xin, Yongyang Wei, Weidong Xiao

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in Computational and mathematical methods in medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Iron as a therapeutic target in chronic liver disease.World journal of gastroenterology · 2023
    Review
  5. Article
  6. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Yuanpeng XiongDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Yonghao OuyangDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Kang FangDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Gen SunDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Shuju TuDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Wanpeng XinDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Yongyang WeiDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Weidong XiaoDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China.ORCID https://orcid.org/0000-0003-3266-6440
Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: As an iron-dependent type of programmed cell death, ferroptosis plays an important role in the pathogenesis and progression of hepatocellular carcinoma (HCC). Long noncoding RNAs (lncRNAs) have been linked to the prognosis of patients with HCC in a number of studies. Nevertheless, the predictive value of lncRNAs (FRLs) associated with ferroptosis in HCC has not been fully elucidated. Methods: Download RNA sequencing data and clinical profiles of HCC patients from The Cancer Genome Atlas (TCGA) database. The FRLs associated with prognosis were determined by Pearson's correlation analysis. After that, prognostic signature for FRLs was established using Cox and LASSO regression analyses. Meanwhile, survival analysis, correlation analysis of clinicopathological features, Cox regression, receiver operating characteristic (ROC) curve, and nomogram were used to analyze the FRL signature's predictive capacity. The relationship between signature risk score, immune cell infiltration, and chemotherapy drug sensitivity is further studied. Results: In total, 93 FRLs were found to be of prognostic value in patients with HCC. A five-FRL signature comprising AC015908.3, LINC01138, AC009283.1, Z83851.1, and LUCAT1 was created in order to enhance the prognosis prediction with HCC patients. The signature demonstrated a good predictive potency, according to the Kaplan-Meier and ROC curves. The five-FRL signature was found to be a risk factor independent of various clinical factors using Cox regression and stratified survival analysis. The high-risk group was shown to be enriched in tumorigenesis and immune-related pathways according to GSEA analysis. Additionally, immune cell infiltration, immune checkpoint molecules, and half-inhibitory concentrations differed considerably between risk groups, implying that this signature could be used to evaluate the clinical efficacy of chemotherapy and immunotherapy. Conclusion: The five-FRL risk signature is helpful for assessing the prognosis of HCC patients and improving therapy options, so it can be further applied clinically.

Indexed as

Carcinoma, HepatocellularFerroptosisLiver NeoplasmsRNA, Long NoncodingComputational BiologyGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimatePrognosisRNA, Long Noncoding

Identifiers

PMID35774297
PMCPMC9239824
OpenAlexW4283274892

What Socratic holds

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LicenceCC BY
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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 Socratic graph.