Evidence map›Paper›PMID 42340577›Full record

ArticleMolecular biology reports2026

Protective role of ginger nanoparticles against hepatocellular carcinoma through regulation of DNA methylation and miRNA-34a-mediated apoptosis.

Noha Nabil Mohamed, Samy Ali Hussein, Yakout Abdelfatah El-Senosi, Mahmoud Abdelghaffar Emam, Shawky Ahmed Moustafa, Fatma M El-Tantawy

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Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Noha Nabil MohamedDepartment of Biochemistry and molecular biology, Faculty of Veterinary Medicine, Benha University, Benha, Egypt.ORCID http://orcid.org/0009-0007-3699-2645
Samy Ali HusseinDepartment of Biochemistry and molecular biology, Faculty of Veterinary Medicine, Benha University, Benha, Egypt.
Yakout Abdelfatah El-SenosiDepartment of Biochemistry and molecular biology, Faculty of Veterinary Medicine, Benha University, Benha, Egypt.
Mahmoud Abdelghaffar EmamDepartment of Histology, Faculty of Veterinary Medicine, Benha University, Benha, Egypt.ORCID http://orcid.org/0000-0003-0515-8125
Shawky Ahmed MoustafaDepartment of pathology, Faculty of Veterinary Medicine, Benha University, Benha, Egypt.ORCID http://orcid.org/0000-0003-4487-8133
Fatma M El-TantawyUrology and Nephrology Center, Mansoura University, Mansoura, Egypt. fatmamansour@mans.edu.eg.ORCID http://orcid.org/0000-0002-3061-8122

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is a common, aggressive, and potentially fatal malignancy. Ginger possesses a wide range of beneficial biological effects on different body organs. The present study investigated the therapeutic effects of ginger extract (GE) and ginger nanoparticles (GNPs) against HCC induced by diethylnitrosamine (DEN) and carbon tetrachloride (CCl₄).

methodsTreatment was initiated 15 weeks after HCC induction and continued for six consecutive weeks. Forty rats were equally divided into four groups. Group 1 (normal control): rats received saline; Group 2 (DEN/CCl₄): HCC-induced rats; Group 3 (HCC + GE): HCC-induced rats treated with ginger extract (300 mg/kg body weight/day); and Group 4 (HCC + GNPs): HCC-induced rats treated with ginger nanoparticles (50 mg/kg body weight/day). Liver function enzymes and gene expression levels were assessed in blood and tissue samples.

resultsThe HCC-induced group showed a significant elevation in liver marker enzymes, global DNA hypermethylation, upregulation of HAT1 and HDAC4, and downregulation of miRNA-34a expression. In contrast, treatment with GE or GNPs resulted in significant global DNA hypomethylation, downregulation of HAT1 and HDAC4, and upregulation of hepatic miRNA-34a expression.

conclusionThe findings suggest that GE and GNPs suppress hepatocarcinogenesis, potentially through activation of the miRNA-34a pathway involved in apoptosis regulation.

Indexed as

Carcinoma, HepatocellularDNA MethylationLiver NeoplasmsMicroRNAsNanoparticlesPlant ExtractsZingiber officinaleAnimalsApoptosisCarbon TetrachlorideDiethylnitrosamineGene Expression Regulation, NeoplasticMaleRatsCarbon TetrachlorideDiethylnitrosamineMicroRNAsMIRN34 microRNA, ratPlant ExtractsDNA methylationGingerGinger nanoparticlesHepatocarcinogenesisHistone modificationMiRNA-34a

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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.