Evidence map›Paper›PMID 23873026›Full record

ArticleOncogene2014

Prdm5 suppresses Apc(Min)-driven intestinal adenomas and regulates monoacylglycerol lipase expression.

G G Galli, H A Multhaupt, M Carrara, K H de Lichtenberg, I B J Christensen, D Linnemann, E Santoni-Rugiu, R A Calogero, A H Lund

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-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

20 citing papers in PubMed, 26 citations in OpenAlex.

  1. PRDM Proteins Orchestrate Colorectal Cancer Tumorigenesis.International journal of molecular sciences · 2026
    Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Multifaceted Role of PRDM Proteins in Human Cancer.International journal of molecular sciences · 2020
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Emerging role of PR domain containing 5 (PRDM5) as a broad tumor suppressor in human cancers.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
  17. The Endocannabinoid Signaling System in the CNS: A Primer.International review of neurobiology · 2015
    Review
  18. Review
  19. Article
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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

9 authors at 4 institutions in 2 countries.

G G GalliBiotech Research and Innovation Centre, Centre for Epigenetics, University of Copenhagen, Copenhagen, Denmark.
H A MulthauptDepartment of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
M CarraraDepartment of Clinical and Biological Sciences, Molecular Biotechnology Center, University of Torino, Torino, Italy.
K H de LichtenbergBiotech Research and Innovation Centre, Centre for Epigenetics, University of Copenhagen, Copenhagen, Denmark.
I B J ChristensenThe Finsen Laboratory, Faculty of Health Sciences, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
D LinnemannDepartment of Pathology, Herlev Hospital, Herlev, Denmark.
E Santoni-RugiuDepartment of Pathology, Diagnostic Center, Righospitalet, Copenhagen, Denmark.
R A CalogeroDepartment of Clinical and Biological Sciences, Molecular Biotechnology Center, University of Torino, Torino, Italy.
A H LundBiotech Research and Innovation Centre, Centre for Epigenetics, University of Copenhagen, Copenhagen, Denmark.ORCID 0000000274073398
University of Copenhagen · DKUniversity of Turin · ITHerlev Hospital · DKRigshospitalet · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PRDM proteins are tissue-specific transcription factors often deregulated in diseases, particularly in cancer where different members have been found to act as oncogenes or tumor suppressors. PRDM5 is a poorly characterized member of the PRDM family for which several studies have reported a high frequency of promoter hypermethylation in cancer types of gastrointestinal origin. We report here the characterization of Prdm5 knockout mice in the context of intestinal carcinogenesis. We demonstrate that loss of Prdm5 increases the number of adenomas throughout the murine small intestine on an Apc(Min) background. By using the genome-wide ChIP-seq (chromatin immunoprecipitation (ChIP) followed by DNA sequencing) and transcriptome analyses we identify loci encoding proteins involved in metabolic processes as prominent PRDM5 targets and characterize monoacylglycerol lipase (Mgll) as a direct PRDM5 target in human colon cancer cells and in Prdm5 mutant mouse intestines. Moreover, we report the downregulation of PRDM5 protein expression in human colon neoplastic lesions. In summary, our data provide the first causal link between Prdm5 loss and intestinal carcinogenesis, and uncover an extensive and novel PRDM5 target repertoire likely facilitating the tumor-suppressive functions of PRDM5.

Indexed as

AdenomaAdenomatous Polyposis ColiAnimalsCaco-2 CellsCarcinogenesisCell Line, TumorDNA-Binding ProteinsDown-RegulationHumansIntestinal NeoplasmsMiceMonoacylglycerol LipasesMutationTranscription FactorsTranscription, GeneticTranscription Initiation SiteDNA-Binding ProteinsMonoacylglycerol LipasesPRDM5 protein, humanPRDM5 protein, mouseTranscription Factors

Identifiers

PMID23873026
OpenAlexW1997725315

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.