Evidence map›Paper›PMID 35654826›Full record

ArticleCommunications biology2022

Chromosome-specific retention of cancer-associated DNA hypermethylation following pharmacological inhibition of DNMT1.

Ashley K Wiseman, Rochelle L Tiedemann, Huihui Fan, Hui Shen, Zachary Madaj, Michael T McCabe, Melissa B Pappalardi, Peter A Jones

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

9 citing papers in PubMed, 9 citations in OpenAlex.

  1. Structure-guided design of 7-azaindole DNMT1 inhibitors active against hypomethylating agent-resistant acute myeloid leukemia.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  9. The Molecular Gut-Brain Axis in Early Brain Development.International journal of molecular sciences · 2022
    Review
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

8 authors at 3 institutions in 1 country.

Ashley K WisemanDepartment of Epigenetics, Van Andel Institute, Grand Rapids, MI, 49503, USA.
Rochelle L TiedemannDepartment of Epigenetics, Van Andel Institute, Grand Rapids, MI, 49503, USA.
Huihui FanCenter for Precision Health, School of Biomedical Informatics, The University of Texas Health Science Center at Houston, Houston, TX, 77030, USA.ORCID 0000-0003-4233-5389
Hui ShenDepartment of Epigenetics, Van Andel Institute, Grand Rapids, MI, 49503, USA.
Zachary MadajDepartment of Epigenetics, Van Andel Institute, Grand Rapids, MI, 49503, USA.
Michael T McCabeCancer Epigenetics Research Unit, Oncology R&D, GlaxoSmithKline, Collegeville, PA, USA.ORCID 0000-0001-5715-9563
Melissa B PappalardiCancer Epigenetics Research Unit, Oncology R&D, GlaxoSmithKline, Collegeville, PA, USA.ORCID 0000-0001-8457-1625
Peter A JonesDepartment of Epigenetics, Van Andel Institute, Grand Rapids, MI, 49503, USA. Peter.Jones@vai.org.ORCID 0000-0001-8309-4767
Van Andel Institute · USGlaxoSmithKline (United States) · USThe University of Texas Health Science Center at Houston · US

Funding

Targeting DNA Methylation and the Cancer EpigenomeR35CA209859 · NCI · VAN ANDEL RESEARCH INSTITUTE · PI PETER A JONES · 2017 to 2026
$11.9M
NCI NIH HHS R35 CA209859
6 · The paper itself

Abstract

The DNA methylation status of the X-chromosome in cancer cells is often overlooked because of computational difficulties. Most of the CpG islands on the X-chromosome are mono-allelically methylated in normal female cells and only present as a single copy in male cells. We treated two colorectal cancer cell lines from a male (HCT116) and a female (RKO) with increasing doses of a DNA methyltransferase 1 (DNMT1)-specific inhibitor (GSK3685032/GSK5032) over several months to remove as much non-essential CpG methylation as possible. Profiling of the remaining DNA methylome revealed an unexpected, enriched retention of DNA methylation on the X-chromosome. Strikingly, the identified retained X-chromosome DNA methylation patterns accurately predicted de novo DNA hypermethylation in colon cancer patient methylomes in the TCGA COAD/READ cohort. These results suggest that a re-examination of tumors for X-linked DNA methylation changes may enable greater understanding of the importance of epigenetic silencing of cancer related genes.

Indexed as

DNA MethylationNeoplasmsCpG IslandsDNAFemaleHumansMaleX ChromosomeDNA

Identifiers

PMID35654826
PMCPMC9163065
OpenAlexW4282008551

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.