Evidence map›Paper›PMID 40726620›Full record

ArticleJournal of hepatocellular carcinoma2025

Exploring Autophagy-Related Gene Expression in Hepatocellular Carcinoma via TCGA, GEPIA2, and HPA Databases: Implications for Prognosis.

Xiangran Gu, Yuan Chen, Xinyue Hu, Yunhui Li, Renlong Zhu, Hongxu Li, Zhengrong Yuan, Yajie Wang

Abstract read
In one paragraph

Article in Journal of hepatocellular carcinoma, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. [Ursolic acid inNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2026
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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.

Xiangran Gu *College of Biological Sciences and Technology, Beijing Forestry University, Beijing, People's Republic of China.
Yuan Chen *Department of Clinical Laboratory, Peking University Ditan Teaching Hospital, Beijing, People's Republic of China.ORCID 0009-0002-3167-9151
Xinyue Hu *College of Biological Sciences and Technology, Beijing Forestry University, Beijing, People's Republic of China.
Yunhui LiDepartment of Clinical Laboratory, Beijing Ditan Hospital, Capital Medical University, Beijing, People's Republic of China.
Renlong ZhuDepartment of Clinical Laboratory, Peking University Ditan Teaching Hospital, Beijing, People's Republic of China.
Hongxu LiCollege of Biological Sciences and Technology, Beijing Forestry University, Beijing, People's Republic of China.ORCID 0009-0004-7912-3800
Zhengrong YuanCollege of Biological Sciences and Technology, Beijing Forestry University, Beijing, People's Republic of China.ORCID 0000-0002-5175-0675
Yajie WangDepartment of Clinical Laboratory, Peking University Ditan Teaching Hospital, Beijing, People's Republic of China.ORCID 0000-0002-3285-2537

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This study aimed to identify autophagy-related genes (ARGs) with prognostic significance in hepatocellular carcinoma (HCC) using bioinformatics and survival analysis. Materials and Methods: ARGs were sourced from multiple references, including the Human Autophagy Database (HADb), relevant literatures, the Gene Set Enrichment Analysis (GSEA), and a final list was confirmed after eliminating duplicate entries. Differential expression analysis between normal and tumor tissues relied on data from The Cancer Genome Atlas (TCGA). Subsequently, the univariate and multivariate Cox regression analysis, along with the Kaplan-Meier survival analysis, were conducted to identify survival-associated genes. These findings were cross-validated using the Gene Expression Profiling Interactive Analysis 2 (GEPIA2) database and the Human Protein Atlas (HPA) database. Furthermore, expression levels of randomly selected ARGs were validated in HCC and normal cell lines using Real-time quantitative PCR (RT-qPCR), confirming bioinformatics findings. Results: 41 ARGs were pinpointed. The bioinformatics analysis revealed elevated expression levels of these genes in HCC tissues compared to normal tissues. Notably, mRNA expression levels of ARGs were markedly higher in the tumor tissue samples than in the normal liver tissue samples. This observation was corroborated by data from the GEPIA2 and HPA databases, except for Conclusion: This study showed that the 41 obtained ARGs, such as

Indexed as

autophagybioinformaticshepatocellular carcinomaprognostic markersTCGA

Identifiers

PMID40726620
PMCPMC12301253

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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.