Evidence mapPaperPMID 42496533Full record

ReviewEpigenomes2026

Epigenetic Mechanisms of Breast and Ovarian Cancer Development: Interplay Between DNA Methylation/Demethylation Enzymes, MicroRNAs, and Long Non-Coding RNAs.

Svetlana S Lukina, Irina V Pronina, Alexander A Bril, Alexey M Burdennyy, Vitaly I Loginov, Sergey G Morozov

Abstract readReview
In one paragraph

Review in Epigenomes, 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

6 authors.

Svetlana S LukinaInstitute of General Pathology and Pathophysiology, 125315 Moscow, Russia.ORCID 0000-0001-6246-2444
Irina V ProninaFaculty of Natural Sciences, Federal State University of Education, 105005 Moscow, Russia.ORCID 0000-0002-0423-7801
Alexander A BrilInstitute of General Pathology and Pathophysiology, 125315 Moscow, Russia.
Alexey M BurdennyyInstitute of General Pathology and Pathophysiology, 125315 Moscow, Russia.ORCID 0000-0002-9398-8075
Vitaly I LoginovInstitute of General Pathology and Pathophysiology, 125315 Moscow, Russia.ORCID 0000-0003-2668-8096
Sergey G MorozovInstitute of General Pathology and Pathophysiology, 125315 Moscow, Russia.

Funding

Scientific Research Program 2025-2030 (Russian Federation) Scientific Research Program 2025-2030 grant No. FGFU-2025-0010 (Russian Federation)
6 · The paper itself

Abstract

Structural and functional disruptions of the epigenome are hallmarks of breast and ovarian carcinogenesis. This review dissects the reciprocal regulatory networks co-operated by DNA methyltransferases (DNMTs), ten-eleven translocation enzymes (TETs), and key non-coding RNAs (microRNAs and lncRNAs). We map the precise molecular mechanisms through which these epigenetic modulators alter chromatin accessibility, drive transcriptional reprogramming, and promote phenotypic plasticity in hormone-dependent malignancies. By systematically contrasting the distinct yet overlapping epigenetic profiles of breast and ovarian tumors, we elucidate how these aberrations dictate clinical outcomes. This comprehensive synthesis offers critical insights into the dual utility of these epigenetic elements as dual-purpose diagnostic biomarkers and druggable therapeutic targets, laying the groundwork for next-generation targeted epigenetical therapies.

Indexed as

breast cancer (BC)DNA methyltransferases (DNMTs)long non-coding RNAs (lncRNAs)microRNAs (miRNAs)ovarian cancer (OC)ten-eleven translocation enzymes (TET)

Identifiers

PMID42496533
PMCPMC13398234

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.