Evidence map›Paper›PMID 32198884›Full record

ArticleNucleic acids research2020

The genomic landscape of 8-oxodG reveals enrichment at specific inherently fragile promoters.

Francesca Gorini, Giovanni Scala, Giacomo Di Palo, Gaetano Ivan Dellino, Sergio Cocozza, Pier Giuseppe Pelicci, Luigi Lania, Barbara Majello, Stefano Amente

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.9field-weighted citation impact, top 8% of its field
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

39 citing papers in PubMed, 61 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Francesca GoriniDepartment of Molecular Medicine and Medical Biotechnologies, University of Naples 'Federico II', Naples, Italy.
Giovanni ScalaDepartment of Biology, University of Naples 'Federico II', Naples, Italy.
Giacomo Di PaloDepartment of Molecular Medicine and Medical Biotechnologies, University of Naples 'Federico II', Naples, Italy.
Gaetano Ivan DellinoDepartment of Experimental Oncology, IEO, European Institute of Oncology IRCCS, Milan, Italy.
Sergio CocozzaDepartment of Molecular Medicine and Medical Biotechnologies, University of Naples 'Federico II', Naples, Italy.
Pier Giuseppe PelicciDepartment of Experimental Oncology, IEO, European Institute of Oncology IRCCS, Milan, Italy.
Luigi LaniaDepartment of Molecular Medicine and Medical Biotechnologies, University of Naples 'Federico II', Naples, Italy.
Barbara MajelloDepartment of Biology, University of Naples 'Federico II', Naples, Italy.
Stefano AmenteDepartment of Molecular Medicine and Medical Biotechnologies, University of Naples 'Federico II', Naples, Italy.
University of Naples Federico II · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

8-Oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG) is the most common marker of oxidative stress and its accumulation within the genome has been associated with major human health issues such as cancer, aging, cardiovascular and neurodegenerative diseases. The characterization of the different genomic sites where 8-oxodG accumulates and the mechanisms underlying its formation are still poorly understood. Using OxiDIP-seq, we recently derived the genome-wide distribution of 8-oxodG in human non-tumorigenic epithelial breast cells (MCF10A). Here, we identify a subset of human promoters that accumulate 8-oxodG under steady-state condition. 8-oxodG nucleotides co-localize with double strand breaks (DSBs) at bidirectional and CG skewed promoters and their density correlate with RNA Polymerase II co-occupancy and transcription. Furthermore, by performing OxiDIP-seq in quiescent (G0) cells, we found a strong reduction of oxidatively-generated damage in the majority of 8-oxodG-positive promoters in the absence of DNA replication. Overall, our results suggest that the accumulation of 8-oxodG at gene promoters occurs through DNA replication-dependent or -independent mechanisms, with a possible contribution to the formation of cancer-associated translocation events.

Indexed as

Genomic InstabilityPromoter Regions, Genetic8-Hydroxy-2'-DeoxyguanosineBase CompositionCell LineDNADNA Breaks, Double-StrandedDNA GlycosylasesDNA RepairDNA ReplicationGenome, HumanHumansPoly (ADP-Ribose) Polymerase-1Transcription, Genetic8-Hydroxy-2'-DeoxyguanosineDNADNA Glycosylasesoxoguanine glycosylase 1, humanPARP1 protein, humanPoly (ADP-Ribose) Polymerase-1

Identifiers

PMID32198884
PMCPMC7192600
OpenAlexW3012713189

What OpenQuestion holds

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LicenceCC BY-NC
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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.