Evidence map›Paper›PMID 36406193›Full record

ArticleWorld journal of oncology2022

A Novel Cuproptosis-Related Signature Identified DLAT as a Prognostic Biomarker for Hepatocellular Carcinoma Patients.

Wen Dong Bai, Jun Yu Liu, Miao Li, Xi Yang, Yu Lan Wang, Guang Jun Wang, Shi Chao Li

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Article in World journal of oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
5.0field-weighted citation impact, top 3% 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

21 citing papers in PubMed, 33 citations in OpenAlex.

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  3. 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

7 authors at 3 institutions in 1 country.

Wen Dong BaiDepartment of Hematology, General Hospital of Xinjiang Military Command, Urumqi, Xinjiang, China.
Jun Yu LiuDepartment of Gastroenterology, Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510060, China.
Miao LiSchool of Rehabilitation Medicine, Xinjiang Medical University, Urumqi, Xinjiang, China.
Xi YangDepartment of Medical Service, General Hospital of Xinjiang Military Command, Urumqi, Xinjiang, China.
Yu Lan WangDepatment of Pathology, General Hospital of Xinjiang Military Command, Urumqi, Xinjiang, China.
Guang Jun WangDepartment of Medical Service, General Hospital of Xinjiang Military Command, Urumqi, Xinjiang, China.
Shi Chao LiDepatment of Pathology, General Hospital of Xinjiang Military Command, Urumqi, Xinjiang, China.
Karamay Central Hospital of Xinjiang · CNSun Yat-sen University · CNXinjiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hepatocellular carcinoma (HCC) is the most common type of liver cancers, with more than a million cases per year by 2025. Cuproptosis is a novel form of programmed cell death, and is caused by mitochondrial lipoylation and destabilization of iron-sulfur proteins triggered by copper, which was considered as a key player in various biological processes. However, the roles of cuproptosis-related genes (CRGs) in HCC remain largely unknown. Methods: In the present study, we constructed and validated a four CRGs signature for predicting the overall survival (OS) of HCC patients in both The Cancer Genome Atlas (TCGA) and International Cancer Genome Consortium (ICGC) databases. Results: Patients with high CRGs risk score showed shorter OS than those with low CRGs risk score. Functional analysis suggested that the CRGs-based prognostic signature was associated with metabolism remodeling which facilitated liver cancer progression. In addition, reduced infiltration of CD8 Conclusion: In conclusion, our study constructed a four CRGs signature prognostic model and identified DLAT as an independent prognostic factor for HCC, thus providing new clues for understanding the association between cuproptosis and HCC.

Indexed as

BiomarkerCuproptosisDLATHepatocellular carcinoma

Identifiers

PMID36406193
PMCPMC9635792
OpenAlexW4307101074

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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.