Evidence map›Paper›PMID 24389641›Full record

ReviewActa biochimica et biophysica Sinica2014

Regulation of protein stability of DNA methyltransferase 1 by post-translational modifications.

Anthony Scott, Jing Song, Rob Ewing, Zhenghe Wang

Abstract readReview
In one paragraph

Review in Acta biochimica et biophysica Sinica, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Article
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  8. NOS2 andProceedings of the National Academy of Sciences of the United States of America · 2022
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  14. Review
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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

4 authors.

Anthony ScottDepartment of Genetics and Genome Sciences, Case Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH 44106, USA.
Jing Song
Rob Ewing
Zhenghe Wang

Funding

TUMOR METABOLISM PROGRAMP30CA043703 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MARK R CHANCE · 1987 to 2026
$142.3M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007250 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI HUANG, ALEX YEE-CHEN · 1985 to 2023
$33.4M
Targeting 15-PGDH in Colon Cancer Prognosis, Prediction, Treatment and PreventionP50CA150964 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MARKOWITZ, SANFORD D. · 2011 to 2022
$24.6M
Mechanisms of suppression of colon cancer by receptor tyrosine phosphatase PTPRTR01CA127590 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI WANG, ZHENGHE · 2007 to 2017
$2.9M
Training Programs in Cancer PharmacologyR25CA148052 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI NOY, NOA · 2010 to 2014
$2.1M
Next-generation mouse gene-targeting technology to model tumorigenesisR21CA181859 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI WANG, ZHENGHE · 2013 to 2015
$682k
Developing novel technology for mapping dynamic oncoprotein interaction networksR21CA160060 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI WANG, ZHENGHE · 2012 to 2013
$464k
NCI NIH HHS P30 CA043703NCI NIH HHS P50 CA150964NCI NIH HHS P50CA150964NCI NIH HHS R01 CA127590NCI NIH HHS R01CA127590NCI NIH HHS R21 CA160060NCI NIH HHS R21CA160060NCI NIH HHS R21 CA181859NCI NIH HHS R25 CA148052NIGMS NIH HHS T32 GM007250
6 · The paper itself

Abstract

DNA methylation is an important epigenetic mechanism that ensures correct gene expression and maintains genetic stability. DNA methyltransferase 1 (DNMT1) is the primary enzyme that maintains DNA methylation during replication. Dysregulation of DNMT1 is implicated in a variety of diseases. DNMT1 protein stability is regulated via various post-translational modifications, such as acetylation and ubiquitination, but also through protein-protein interactions. These mechanisms ensure DNMT1 is properly activated during the correct time of the cell cycle and at correct genomic loci, as well as in response to appropriate extracellular cues. Further understanding of these regulatory mechanisms may help to design novel therapeutic approaches for human diseases.

Indexed as

DNA MethylationProtein Processing, Post-TranslationalAntineoplastic Combined Chemotherapy ProtocolsAzacitidineDNA (Cytosine-5-)-Methyltransferase 1DNA (Cytosine-5-)-MethyltransferasesHumansHydroxamic AcidsNeoplasmsProtein StabilityVorinostatAzacitidineDNA (Cytosine-5-)-Methyltransferase 1DNA (Cytosine-5-)-MethyltransferasesDNMT1 protein, humanHydroxamic AcidsVorinostatDNA (cytosine-5-)-methyltransferaseepi-geneticsneoplasmspost-translational modificationprotein stability

Identifiers

PMID24389641
PMCPMC3932833

What OpenQuestion holds

Textmetadata
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.