Evidence map›Paper›PMID 36159561›Full record

ArticleEvidence-based complementary and alternative medicine : eCAM2022

A Noval Established Cuproptosis-Associated LncRNA Signature for Prognosis Prediction in Primary Hepatic Carcinoma.

Lan Luo, Xiaoyan Hu, Aoshuang Huang, Xiaofang Liu, Lingyun Wang, Tao Du, Lei Liu, Ming Li

Abstract read
In one paragraph

Article in Evidence-based complementary and alternative medicine : eCAM, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

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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

11 citing papers in PubMed.

  1. Review
  2. Targeting cuproptosis in liver cancer: Molecular mechanisms and therapeutic implications.Apoptosis : an international journal on programmed cell death · 2025
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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

8 authors.

Lan LuoDepartment of Hematology and Oncology, The First People's Hospital of Guiyang, No. 97, Boai Road, Nanming, Guiyang, Guizhou 550002, China.ORCID https://orcid.org/0000-0002-7166-2381
Xiaoyan HuDepartment of Hematology and Oncology, The First People's Hospital of Guiyang, No. 97, Boai Road, Nanming, Guiyang, Guizhou 550002, China.
Aoshuang HuangDepartment of Hematology and Oncology, The First People's Hospital of Guiyang, No. 97, Boai Road, Nanming, Guiyang, Guizhou 550002, China.
Xiaofang LiuDepartment of Hematology and Oncology, The First People's Hospital of Guiyang, No. 97, Boai Road, Nanming, Guiyang, Guizhou 550002, China.
Lingyun WangDepartment of Hematology and Oncology, The First People's Hospital of Guiyang, No. 97, Boai Road, Nanming, Guiyang, Guizhou 550002, China.
Tao DuDepartment of Hematology and Oncology, The First People's Hospital of Guiyang, No. 97, Boai Road, Nanming, Guiyang, Guizhou 550002, China.
Lei LiuDepartment of Hematology and Oncology, The First People's Hospital of Guiyang, No. 97, Boai Road, Nanming, Guiyang, Guizhou 550002, China.
Ming LiDepartment of Hematology and Oncology, The First People's Hospital of Guiyang, No. 97, Boai Road, Nanming, Guiyang, Guizhou 550002, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The copper ion content in the body maintains homeostasis, and when dysregulated, it can produce cytotoxicity and induce cell death through a variety of pathways. Cuproptosis refers to copper ions combining directly with acylated molecules, leading to the accumulation of oligomerization of lipoylated protein and subsequent downregulation of iron-sulfur cluster proteins; this induces proteotoxic stress and cell death. This study on the relationship between cuproptosis-related lncRNAs (CRLns) and the prognosis of primary hepatic carcinoma (PHC) has important clinical guiding significance for the diagnosis and treatment of PHC. Prognosis-related CRLRs were identified via rank-sum tests, correlational analyses, and univariate Cox regression, and a CRLR risk-scoring model (CRLRSM) was constructed using LASSO Cox regression. Patients were divided into high-risk and low-risk groups based on the median CRLRSM scores. Variance analysis for cuproptosis-related genes, gene set enrichment analysis, and correlational analysis for risk and immunity were performed using boxplots. Quantitative polymerase chain reactions were used to verify the CRLR levels in PHC cell lines. The study results showed that patients in the CRLRSM high-risk group had worse survival rates than those in the low-risk group. The PHC stage and risk score were independent prognostic factors for hepatocellular carcinoma. There were 7 CRLRs (MIR210HG, AC099850.3, AL031985.3, AC012073.1, MKLN1-AS, KDM4A-AS1, and PLBD1-AS1) associated with PHC prognosis, primarily through cellular metabolism, growth, proliferation, apoptosis, and immunity. In conclusion, the overexpression of 7 CRLRs in patients with PHC indicates a poor prognosis.

Identifiers

PMID36159561
PMCPMC9499762

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