Evidence map›Paper›PMID 39430854›Full record

ArticleTranslational cancer research2024

Comprehensive analysis of cuproptosis-related genes involved in prognosis and tumor microenvironment infiltration of colorectal cancer.

Weiyi Chen, Ke Hu, Yu Liu, Xiaocheng Li, Lijun Chen, Shaoyi Duan, Qizhang Yang

Abstract read
In one paragraph

Article in Translational cancer research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Interaction of HIF-1a with various cell death pathways in tumor immune microenvironment (TIME).Apoptosis : an international journal on programmed cell death · 2026
    Pooled it
  2. Article
  3. Review
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.

Weiyi ChenDepartment of Medicine, Department of Basic Medicine, Hunan University of Medicine, Huaihua, China.
Ke HuDepartment of Medicine, Department of Basic Medicine, Hunan University of Medicine, Huaihua, China.
Yu LiuDepartment of Medicine, Department of Basic Medicine, Hunan University of Medicine, Huaihua, China.
Xiaocheng LiDepartment of General Surgery, The First Affiliated Hospital of Hunan University of Medicine, Huaihua, China.
Lijun ChenDepartment of Medicine, Department of Basic Medicine, Hunan University of Medicine, Huaihua, China.
Shaoyi DuanDepartment of Medicine, Department of Basic Medicine, Hunan University of Medicine, Huaihua, China.
Qizhang YangDepartment of Medicine, Department of Basic Medicine, Hunan University of Medicine, Huaihua, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Colorectal cancer (CRC) is a common malignancy, with high incidence and high mortality rates. Cuproptosis, a novel form of copper-induced programmed cell death, contributes to tumor progression. However, whether cuproptosis-related genes (CRGs) play a role in CRC remains unclear. This study aims to elucidate the role of CRGs in CRC development, patient prognosis, and immune response. Methods: We performed bioinformatics analysis of the differential expression of CRGs between CRC and normal tissues. Least absolute shrinkage and selection operator (LASSO), and univariate and multivariate Cox analyses were employed to identify risk factors, which were used to construct a risk score model. Patients with CRC were categorized into high- and low-risk groups based on their median risk scores. Receiver operating characteristic curve analysis was used to verify the predictive accuracy of the risk model. A nomogram was developed for CRC through univariate and multivariate Cox regression analyses. The chemotherapeutic drug sensitivity was compared between patients with high and low Results: Eight of ten identified CRGs exhibited significant differential expression between CRC and normal tissues. Among the eight significant differential expression CRGs, Conclusions: Our research revealed the prognostic value of CRGs, particularly

Indexed as

colorectal cancer (CRC)Cuproptosisgene signatureimmune infiltrationoverall survival (OS)

Identifiers

PMID39430854
PMCPMC11483459

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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.