Evidence map›Paper›PMID 36750831›Full record

ArticleBiology direct2023

Identification of a prognostic cuproptosis-related signature in hepatocellular carcinoma.

Yuqiao Chen, Lu Tang, Wentao Huang, Fakolade Hannah Abisola, Youyu Zhang, Gewen Zhang, Lei Yao

Open access · goldAbstract read
In one paragraph

Article in Biology direct, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
17.6field-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

55 citing papers in PubMed, 66 citations in OpenAlex.

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  14. Disulfidptosis-related genes RPN1 inhibits the progression of hepatocellular carcinoma by regulating cell cycle, may be a new therapeutic targets.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Article
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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

7 authors at 2 institutions in 1 country.

Yuqiao ChenDepartment of General Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Lu TangDepartment of Anesthesiology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Wentao HuangDepartment of Thoracic Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Fakolade Hannah AbisolaDepartment of Thoracic Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Youyu ZhangDepartment of Thoracic Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Gewen ZhangDepartment of General Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Lei YaoDepartment of General Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, China. leiyao@csu.edu.cn.
Central South University · CNXiangya Hospital Central South University · CN

Funding

The ChenXiao-ping Foundation for the development of Science and Technology of Hubei Province CXPJJH121003-2109
6 · The paper itself

Abstract

backgroundCuproptosis is a new type of copper-induced cell death that is characterized by the aggregation of lipoylated tricarboxylic acid (TCA) cycle proteins. However, its role in hepatocellular carcinoma (HCC) remains unclear. The goal of this research is to develop a cuproptosis-related signature predicting the prognosis of HCC.

methodsThe cuproptosis-related genes were defined using Pearson correlation coefficients. LASSO-Cox regression analysis was used to evaluate the prognostic values of cuproptosis-related genes to construct a cuproptosis-related prognostic model. The immune microenvironment analysis was performed by "ssGSEA" to reveal the associated immune cell infiltration patterns with the cuproptosis-related genes signature. The expression levels of one of the prognostic genes PDXK were then verified in HCC samples by Western Blot and immunohistochemistry. The potential roles of target genes in cuproptosis were further explored during in-vitro experiments.

resultsA total of 136 cuproptosis-related genes were discovered using Pearson correlation analysis in HCC. A cuproptosis-related signature that included 5 cuproptosis-related genes (PDXK, HPN, SLC25A28, RNFT1, CLEC3B) was established in the TCGA-LIHC training cohort. TCGA validation cohort and another two external validation cohorts confirmed the robustness of the signature's predictive value. Moreover, a nomogram using the risk score was created to best predict the survival of HCC patients. The immune microenvironment analysis revealed distinct immune infiltrations patterns between different risk groups based on the signature model. Furthermore, the upregulation of PDXK was confirmed in HCC tumor tissues in 30 clinical HCC specimens. The knockdown of PDXK reduced the proliferation, migration and invasion of HCC cells. Besides, the expression of PDXK was upregulated after the induction of cuproptosis by elesclomol-CuCL

conclusionOur study identified a new cuproptosis-related gene signature that could predict the prognosis of HCC patient. Besides, the upregulated PDXK could promote the proliferation and metastasis of HCC. And PDXK deficiency facilities cuproptosis in HCC. Therefore, these fundings highlighted that PDXK might serve as a potential diagnostic and therapeutic target for HCC.

Indexed as

ApoptosisCarcinoma, HepatocellularCation Transport ProteinsLiver NeoplasmsCell LineCopperHumansPrognosisTumor MicroenvironmentCation Transport ProteinsCopperSLC25A28 protein, humanBioinformatic analysisCuproptosisHepatocellular carcinomaMetastasisPDXKPrognostic signature

Identifiers

PMID36750831
PMCPMC9903524
OpenAlexW4319439377

What OpenQuestion holds

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LicenceCC BY
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.