Evidence map›Paper›PMID 41376822›Full record

ArticleNon-coding RNA research2026

Integrative analysis of tissue and circulating miRNAs as biomarkers for progression and survival in hepatocellular carcinoma.

Abdullah Jabri, Abdulaziz Mhannayeh, Mohamed Alsharif, Bader Taftafa, Tooba Mujtaba, Arshiya Akbar, Ahmed Abu-Zaid, Tanveer Ahmad Mir, Mohammad Imran Khan, Firoz Ahmed and 2 more

Abstract read
In one paragraph

Article in Non-coding RNA research, 2026. 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

12 authors.

Abdullah JabriCollege of Medicine, Alfaisal University, Riyadh, 11211, Saudi Arabia.
Abdulaziz MhannayehCollege of Medicine, Alfaisal University, Riyadh, 11211, Saudi Arabia.
Mohamed AlsharifCollege of Medicine, Alfaisal University, Riyadh, 11211, Saudi Arabia.
Bader TaftafaCollege of Medicine, Alfaisal University, Riyadh, 11211, Saudi Arabia.
Tooba MujtabaCollege of Medicine, Alfaisal University, Riyadh, 11211, Saudi Arabia.
Arshiya AkbarCollege of Medicine, Alfaisal University, Riyadh, 11211, Saudi Arabia.
Ahmed Abu-ZaidCollege of Medicine, Alfaisal University, Riyadh, 11211, Saudi Arabia.
Tanveer Ahmad MirCollege of Medicine, Alfaisal University, Riyadh, 11211, Saudi Arabia.
Mohammad Imran KhanCollege of Medicine, Alfaisal University, Riyadh, 11211, Saudi Arabia.
Firoz AhmedDepartment of Biological Sciences, College of Science, University of Jeddah, Jeddah, Saudi Arabia.
Itika AroraCollege of Medicine, Alfaisal University, Riyadh, 11211, Saudi Arabia.
Ahmed YaqinuddinCollege of Medicine, Alfaisal University, Riyadh, 11211, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a leading cause of cancer-related mortality, with limited biomarkers available for early diagnosis and risk stratification. In this study, we performed an integrative analysis of tissue and circulating microRNA (miRNA) expression profiles to identify candidates linked to disease progression and clinical outcomes. Tumor miRNA data from The Cancer Genome Atlas Liver Hepatocellular Carcinoma (TCGA-LIHC) and serum miRNA data from the Gene Expression Omnibus (GSE113740) were analyzed using differential expression, survival analysis, functional enrichment, and clinical subgroup evaluation. We identified 16 significantly dysregulated miRNAs in HCC tissues, including hsa-miR-187 and hsa-miR-6718, which were associated with poor survival, and hsa-miR-5589, which showed a protective effect. Clinical analyses revealed stage-specific upregulation of hsa-miR-106b and downregulation of the hsa-miR-124 family in metastatic tumors. Functional enrichment highlighted pathways such as PI3K-Akt, MAPK signalling, and nucleocytoplasmic transport. Circulating miRNAs, including hsa-miR-3619-3p, hsa-miR-1290, and hsa-miR-1185-2-3p, correlated with AFP levels and disease stage, underscoring their value as non-invasive biomarkers. These findings demonstrate that integrated analysis of tissue and serum miRNAs can identify clinically relevant biomarkers and potential therapeutic targets in HCC.

Indexed as

BioinformaticsBiomarkersHepatocellular carcinomamiRNASurvival analysisTCGA

Identifiers

PMID41376822
PMCPMC12686728

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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.