Evidence map›Paper›PMID 40743051›Full record

ArticlePloS one2025

Epigenome and three-dimensional genome architecture remodeling during NDM29-mediated retro-transformation of neuroblastoma cells.

Francesca Baldini, Aldo Pagano, Lama Zeaiter, Paolo Bianchini, Hawraa Zbeeb, Alberto Diaspro, Laura Vergani

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Article in PloS one, 2025. 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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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Francesca BaldiniNanoscopy, Istituto Italiano Tecnologia, Genova, Italy.
Aldo PaganoDIMES, Department of Experimental Medicine, University of Genoa, Genova, Italy.
Lama ZeaiterNanoscopy, Istituto Italiano Tecnologia, Genova, Italy.
Paolo BianchiniNanoscopy, Istituto Italiano Tecnologia, Genova, Italy.
Hawraa ZbeebDISTAV, Department for the Earth, Environment and Life Sciences, University of Genova, Genova, Italy.
Alberto DiasproNanoscopy, Istituto Italiano Tecnologia, Genova, Italy.
Laura VerganiDISTAV, Department for the Earth, Environment and Life Sciences, University of Genova, Genova, Italy.ORCID https://orcid.org/0000-0002-1268-4724

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neoplastic transformation of mammalian cells involves intricate interactions between genetic, epigenetic and architecture modifications of the nucleus. Neuroblastoma is a malignant pediatric tumor with high biological and clinical heterogeneity representing a challenging model of study. We aimed to explore the changes in genome architecture and epigenetics being associated with neuroblastoma malignancy. We employed the neuroblastoma cell line SKNBE2 overexpressing the ncRNA NDM29 to differentiate from highly malignant into neuron-like cells. By 3D confocal microscopy, we explored the nuclear architecture (volume, elongation, compactness, and chromatin density). Using super-resolution microscopy (STED) and histone H3 immunolabelling we assessed the epigenetic rearrangement, and by enzyme-linked immunoassay the global DNA methylation. Then we assessed the mRNA expression of the main epigenetic modifying enzymes by quantitative PCR, and the expression of NF-κB-regulated genes by cDNA microarray. Compared to malignant NB cells, the NDM29-overexpressing cells, assuming a neuron-like phenotype, exhibited smaller and more elongated nuclei, redistribution of H3K9-acetylated and -methylated chromatin domains and DNA hypermethylation. In line with these results, in neuron-like cells the acetyltransferase KAT2A and the DNA methyltransferase DNMT1 were up-regulated, while most of NF-κB-regulated genes were down-regulated. Our findings reveal modifications of the nuclear structure and epigenome during neuroblastoma retro-transformation induced by NDM29 overexpression, with impacts on gene expression. These results offer potential insights into better understanding the mechanism of neuroblastoma malignancy in terms of chromatin rearrangements, opening exciting prospects for prognostic and therapeutic approaches with a focus on the nuclear level.

Indexed as

Epigenesis, GeneticEpigenomeNeuroblastomaCell Line, TumorDNA (Cytosine-5-)-Methyltransferase 1DNA MethylationGene Expression Regulation, NeoplasticHistonesHumansDNA (Cytosine-5-)-Methyltransferase 1Histones

Identifiers

PMID40743051
PMCPMC12312970

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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.