Evidence map›Paper›PMID 22207358›Full record

ArticleEpigenetics2012

The 3D tissue microenvironment modulates DNA methylation and E-cadherin expression in squamous cell carcinoma.

Teresa M DesRochers, Yulia Shamis, Addy Alt-Holland, Yasusei Kudo, Takashi Takata, Guangwen Wang, Laurie Jackson-Grusby, Jonathan A Garlick

Open access · bronzeAbstract read
In one paragraph

Article in Epigenetics, 2012. 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
1.7field-weighted citation impact, top 16% 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

21 citing papers in PubMed, 53 citations in OpenAlex.

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  19. Tissue-engineered kidney disease models.Advanced drug delivery reviews · 2014
    Review
  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

8 authors at 3 institutions in 3 countries.

Teresa M DesRochersDepartment of Anatomy, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, Boston, MA, USA.
Yulia Shamis
Addy Alt-Holland
Yasusei Kudo
Takashi Takata
Guangwen Wang
Laurie Jackson-Grusby
Jonathan A Garlick
Tufts University · USHarvard University · USHiroshima University · JP

Funding

Genomic Imprinting and Embryonic DevelopmentR01HD050760 · NICHD · CHILDREN'S HOSPITAL BOSTON · PI JACKSON-GRUSBY, LAURIE L · 2005 to 2009
$2.0M
Epigenetic Regulation of MedulloblastomaR01CA135454 · NCI · BOSTON CHILDREN'S HOSPITAL · PI JACKSON-GRUSBY, LAURIE L · 2009 to 2012
$1.4M
Pathobiology of the Developing Cardiovascular SystemT32HL076115 · NHLBI · CHILDREN'S HOSPITAL BOSTON · PI FLEMING, MARK D · 2005 to 2009
$970k
NCI NIH HHS R01 CA135454NHLBI NIH HHS T32 HL076115NICHD NIH HHS R01 HD050760NIDCR NIH HHS DE017143
6 · The paper itself

Abstract

The microenvironment plays a significant role in human cancer progression. However, the role of the tumor microenvironment in the epigenetic control of genes critical to cancer progression remains unclear. As transient E-cadherin expression is central to many stages of neoplasia and is sensitive to regulation by the microenvironment, we have studied if microenvironmental control of E-cadherin expression is linked to transient epigenetic regulation of its promoter, contributing to the unstable and reversible expression of E-cadherin seen during tumor progression. We used 3D, bioengineered human tissue constructs that mimic the complexity of their in vivo counterparts, to show that the tumor microenvironment can direct the re-expression of E-cadherin through the reversal of methylation-mediated silencing of its promoter. This loss of DNA methylation results from the induction of homotypic cell-cell interactions as cells undergo tissue organization. E-cadherin re-expression is associated with multiple epigenetic changes including altered methylation of a small number of CpGs, specific histone modifications, and control of miR-148a expression. These epigenetic changes may drive the plasticity of E-cadherin-mediated adhesion in different tissue microenvironments during tumor cell invasion and metastasis. Thus, we suggest that epigenetic regulation is a mechanism through which tumor cell colonization of metastatic sites occurs as E-cadherin-expressing cells arise from E-cadherin-deficient cells.

Indexed as

DNA MethylationGene Expression Regulation, NeoplasticCadherinsCarcinoma, Squamous CellCell CommunicationCell Culture TechniquesCell Line, TumorDNA (Cytosine-5-)-Methyltransferase 1DNA (Cytosine-5-)-MethyltransferasesHistone CodeHistonesHumansMicroRNAsNeoplasm MetastasisPromoter Regions, GeneticTumor MicroenvironmentCadherinsDNA (Cytosine-5-)-Methyltransferase 1DNA (Cytosine-5-)-MethyltransferasesHistonesMicroRNAsMIRN148 microRNA, human

Identifiers

PMID22207358
PMCPMC3329501
OpenAlexW2054475896

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.