Evidence map›Paper›PMID 20587527›Full record

ArticleCancer research2010

DNMT3B7, a truncated DNMT3B isoform expressed in human tumors, disrupts embryonic development and accelerates lymphomagenesis.

Mrinal Y Shah, Aparna Vasanthakumar, Natalie Y Barnes, Maria E Figueroa, Anna Kamp, Christopher Hendrick, Kelly R Ostler, Elizabeth M Davis, Shang Lin, John Anastasi and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

44 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. DNMT Enzymes and Their Impact on Cervical Cancer: A State-of-the-Art Review.International journal of molecular sciences · 2025
    Review
  5. Review
  6. Review
  7. DNA Methyltransferases: From Evolution to Clinical Applications.International journal of molecular sciences · 2022
    Review
  8. Genetic Studies on Mammalian DNA Methyltransferases.Advances in experimental medicine and biology · 2022
    Article
  9. Review
  10. Review
  11. Article
  12. Epigenetics insights · 2020
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

15 authors at 3 institutions in 2 countries.

Mrinal Y ShahSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, Illinois 60637-1470, USA.
Aparna Vasanthakumar
Natalie Y Barnes
Maria E Figueroa
Anna Kamp
Christopher Hendrick
Kelly R Ostler
Elizabeth M Davis
Shang Lin
John Anastasi
Michelle M Le Beau
Ivan P Moskowitz
Ari Melnick
Peter Pytel
Lucy A Godley
Cornell University · USUniversity of Chicago · USInstitute of Molecular Medicine · IN

Funding

The Role of DNMT3B in the DNA Methylation of Cancer CellsR01CA129831 · NCI · UNIVERSITY OF CHICAGO · PI GODLEY, LUCY ANN · 2008 to 2012
$1.8M
NCI NIH HHS R01 CA129831
6 · The paper itself

Abstract

Epigenetic changes are among the most common alterations observed in cancer cells, yet the mechanism by which cancer cells acquire and maintain abnormal DNA methylation patterns is not understood. Cancer cells have an altered distribution of DNA methylation and express aberrant DNA methyltransferase 3B transcripts, which encode truncated proteins, some of which lack the COOH-terminal catalytic domain. To test if a truncated DNMT3B isoform disrupts DNA methylation in vivo, we constructed two lines of transgenic mice expressing DNMT3B7, a truncated DNMT3B isoform commonly found in cancer cells. DNMT3B7 transgenic mice exhibit altered embryonic development, including lymphopenia, craniofacial abnormalities, and cardiac defects, similar to Dnmt3b-deficient animals, but rarely develop cancer. However, when DNMT3B7 transgenic mice are bred with Emicro-Myc transgenic mice, which model aggressive B-cell lymphoma, DNMT3B7 expression increases the frequency of mediastinal lymphomas in Emicro-Myc animals. Emicro-Myc/DNMT3B7 mediastinal lymphomas have more chromosomal rearrangements, increased global DNA methylation levels, and more locus-specific perturbations in DNA methylation patterns compared with Emicro-Myc lymphomas. These data represent the first in vivo modeling of cancer-associated DNA methylation changes and suggest that truncated DNMT3B isoforms contribute to the redistribution of DNA methylation characterizing virtually every human tumor.

Indexed as

Abnormalities, MultipleAnimalsCell Transformation, NeoplasticDNA (Cytosine-5-)-MethyltransferasesDNA MethylationDNA Methyltransferase 3BGene Expression Regulation, DevelopmentalGene Expression Regulation, NeoplasticHumansIsoenzymesLymphomaMediastinal NeoplasmsMiceMice, TransgenicDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3BIsoenzymes

Identifiers

PMID20587527
PMCPMC2905468
OpenAlexW1980194279

What OpenQuestion holds

Textmetadata
LicenceTDM
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.