Evidence map›Paper›PMID 42173694›Full record

ReviewEuropean journal of haematology2026

Epigenetics and In Silico Transcriptome Analysis of Pediatric Acute Myeloid Leukemia.

Akram N Salah, Reda M Mansour, Gharieb S El-Sayyad, Hebatallah Ahmed Mohamed Moustafa, Ghadir A Sayed, Hend H Mohamed, Nourhan H Elshami, Kareem AlFarsi, Ahmed Fahim, Osama A Mohammed and 2 more

Abstract readReview
In one paragraph

Review in European journal of haematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Akram N SalahMicrobiology and Immunology Department, Faculty of Pharmacy, Badr University in Cairo (BUC), Badr City, Egypt.
Reda M MansourMolecular Biology and Biotechnology Department, School of Biotechnology, Badr University in Cairo (BUC), Badr City, Egypt.ORCID https://orcid.org/0000-0002-5546-9020
Gharieb S El-SayyadDepartment of Biology, College of Science, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh, Saudi Arabia.ORCID https://orcid.org/0000-0001-5410-7936
Hebatallah Ahmed Mohamed MoustafaDepartment of Clinical Pharmacy and Pharmacy Practice, Faculty of Pharmacy, Badr University in Cairo (BUC), Badr City, Egypt.
Ghadir A SayedDepartment of Biochemistry, Faculty of Pharmacy, Egyptian Russian University, Badr City, Egypt.
Hend H MohamedSchool of Biotechnology, Badr University in Cairo, Badr City, Egypt.ORCID https://orcid.org/0000-0001-5528-3683
Nourhan H ElshamiDepartment of Microbiology and Immunology, Faculty of Pharmacy, Ain Shams University, Cairo, Egypt.
Kareem AlFarsiDepartment of Pediatric Oncology, Children's Cancer Hospital Egypt (CCHE 57357), Cairo, Egypt.
Ahmed FahimDepartment of Pediatric Oncology, Children's Cancer Hospital Egypt (CCHE 57357), Cairo, Egypt.
Osama A MohammedDepartment of Pharmacology, College of Medicine, University of Bisha, Bisha, Saudi Arabia.ORCID https://orcid.org/0000-0001-9712-9609
Hassan A RudayniDepartment of Biology, College of Science, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh, Saudi Arabia.
Ahmed S DoghishDepartment of Biochemistry, Faculty of Pharmacy, Badr University in Cairo (BUC), Badr City, Egypt.ORCID https://orcid.org/0000-0002-0136-7096

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pediatric acute myeloid leukemia (AML) is a heterogeneous hematologic malignancy that accounts for about 15%-20% of childhood leukemias. Despite therapeutic advances, relapses remain common, and survival for high-risk patients is below 60%. Unlike adult AML, pediatric AML displays distinct genetic mutations, including FLT3-ITD, NPM1, KMT2A rearrangements, and core-binding factors (CBF) fusions, as well as extensive epigenetic dysregulation. Aberrant DNA methylation, histone modifications, and altered non-coding RNA expressions disrupt hematopoietic differentiation and activate oncogenic transcriptional networks. Recent advances in silico transcriptomic analysis have transformed the study of pediatric AML by integrating gene expression and epigenetic data to identify molecular drivers and regulatory networks. Computational RNA-seq pipelines and pathway analyses have highlighted key epigenetic regulators, including DNMT3A, TET2, and HDACs, as potential therapeutic targets. Multi-omics approaches combining transcriptomic, methylomic, and chromatin accessibility data are increasingly used to define biomarkers for diagnosis, prognosis, and therapeutic response. This review provides a comprehensive overview of the molecular and epigenetic landscape of pediatric AML, emphasizing the power of in silico transcriptome analysis to uncover disease mechanisms, refine patient stratification, and guide the development of precision-based epigenetic therapies aimed at improving long-term outcomes in children with AML.

Indexed as

Epigenesis, GeneticEpigenomicsGene Expression ProfilingGene Expression Regulation, LeukemicLeukemia, Myeloid, AcuteTranscriptomeChildComputer SimulationDNA MethylationHumansNucleophosminNPM1 protein, humanNucleophosminepigeneticsin silico analysispediatric AMLtherapeutic targetstranscriptomics

Identifiers

PMID42173694
PMCPMC13542965

What OpenQuestion holds

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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.