Evidence map›Paper›PMID 40717227›Full record

SynthesisJournal of cellular and molecular medicine2025

Circulating miR-542-3p as a Prognostic Marker for Hepatocellular Carcinoma: A Systematic Review and Meta-Analysis.

Ranjith Balakrishnan, Rajasekaran Subbarayan, Maheshkumar Kuppusamy, Rupendra Shrestha, Arunkumar Radhakrishnan, Ankush Chauhan

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Journal of cellular and molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

6 authors.

Ranjith BalakrishnanCentre for Advanced Biotherapeutics and Regenerative Medicine, Faculty of Research, Chettinad Hospital and Research Institute, Chettinad Academy of Research and Education, Kelambakkam, Tamil Nadu, India.
Rajasekaran SubbarayanCentre for Advanced Biotherapeutics and Regenerative Medicine, Faculty of Research, Chettinad Hospital and Research Institute, Chettinad Academy of Research and Education, Kelambakkam, Tamil Nadu, India.ORCID 0000-0001-5890-5273
Maheshkumar KuppusamyDepartment of Physiology & Biochemistry, Government Yoga and Naturopathy Medical College and Hospital, Chennai, Tamil Nadu, India.
Rupendra ShresthaDepartment of Natural and Applied Sciences, Nexus Institute of Research and Innovation (NIRI), Lalitpur, Nepal.ORCID 0000-0001-6804-6070
Arunkumar RadhakrishnanDepartment of Pharmacology, Chettinad Hospital and Research Institute, Chettinad Academy of Research and Education, Kelambakkam, Tamil Nadu, India.
Ankush ChauhanCentre for Herbal Pharmacology and Environmental Sustainability, Chettinad Hospital and Research Institute, Chettinad Academy of Research and Education, Kelambakkam, Tamil Nadu, India.

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 worldwide, particularly in Asia. Despite therapeutic advancements, the prognosis of HCC remains poor. MicroRNAs have emerged as potential biomarkers for HCC prognosis and therapeutic response. This systematic review and meta-analysis examined the association between circulating miR-542-3p levels and HCC progression. Seven studies on HCC and miR-542-3p were selected for the meta-analysis. miR-542-3p showed significant diagnostic potential for HCC prognosis and therapeutic evaluation. Two independent researchers performed data extraction and used the Quality Assessment of Diagnostic Accuracy Studies (QUADAS-2) method to assess the quality and risk of bias of the included studies. After the meta-analysis, human miRNA pattern analysis was conducted using the miRBase database, and the expression of miR-542-3p was confirmed based on the results obtained from the human miRNA profile in the tissue atlas database. miR-542-3p has been shown to have significant diagnostic potential for HCC prognosis and therapeutic evaluation. The pooled sensitivity was 0.79 (95% CI, 0.75-0.83), while the pooled specificity was 0.34 (95% CI, 0.29-0.40). The diagnostic odds ratio was 7.2, with an AUC of 0.806, indicating moderate diagnostic accuracy. Network analysis in miRBase links miR-542-3p to liver function, and its location on the X chromosome allows its expression in both sexes, making it widely applicable for the diagnosis of HCC. Thus, miR-542-3p has potential as a prognostic biomarker for HCC, with prospects for integration into therapeutic strategies. Future studies should explore the combination of this with targeted therapies to improve patient outcomes.

Indexed as

Biomarkers, TumorCarcinoma, HepatocellularLiver NeoplasmsMicroRNAsGene Expression Regulation, NeoplasticHumansPrognosisBiomarkers, TumorMicroRNAsMIRN542 microRNA, humancancer progressionhepatocellular carcinomalivermiR‐542‐3pprognostic biomarker

Identifiers

PMID40717227
PMCPMC12301263

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Registered trials

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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.