Evidence map›Paper›PMID 40530125›Full record

ArticleTranslational cancer research2025

In silico development and validation of a novel six-gene-derived signature in hepatocellular carcinoma.

Jin He, Binbin Li, Huize Liu, Weijian Chu, Chunhui Rao

Abstract read
In one paragraph

Article in Translational cancer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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

1 citing paper in PubMed.

  1. Article
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

5 authors.

Jin HeDepartment of Colorectal Surgery, Hangzhou TCM Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, China.
Binbin LiDepartment of Colorectal Surgery, Hangzhou TCM Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, China.
Huize LiuDepartment of Colorectal Surgery, Hangzhou TCM Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, China.
Weijian ChuDepartment of Colorectal Surgery, Hangzhou TCM Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, China.
Chunhui RaoDepartment of Colorectal Surgery, Hangzhou TCM Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pyruvate metabolism presents a novel, therapeutically targetable metabolic vulnerability in hepatocellular carcinoma (HCC). In this study, we sought to identify HCC molecular subtypes and develop prognostic signatures based on pyruvate metabolism-related genes (PMRGs) to inform personalized therapeutic approaches. Methods: Transcriptional profiles and clinical data of HCC patients were obtained from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) datasets. Consensus clustering was employed for molecular classification, while a least absolute shrinkage and selection operator (LASSO) Cox regression model was constructed for risk score calculation. The relationship between the risk score and HCC prognosis, immune landscape, gene expression, and drug sensitivity was analyzed. Results: Twenty PMRGs were identified as significantly associated with HCC prognosis. Consensus clustering of these genes revealed two distinct molecular subtypes that stratified patients into groups with favorable and unfavorable outcomes. A novel six-gene signature, comprising Conclusions: Collectively, a unique PMRG-based signature effectively predicts prognosis in HCC patients and provides valuable insights into chemotherapy and immunotherapy strategies for these individuals.

Indexed as

consensus clusteringdrug sensitivitieshepatocellular carcinoma (HCC)immune landscapesPyruvate metabolism

Identifiers

PMID40530125
PMCPMC12169999

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.