Evidence map›Paper›PMID 24043307›Full record

ArticleMolecular and cellular biology2013

MEF2 is a converging hub for histone deacetylase 4 and phosphatidylinositol 3-kinase/Akt-induced transformation.

Eros Di Giorgio, Andrea Clocchiatti, Sara Piccinin, Andrea Sgorbissa, Giulia Viviani, Paolo Peruzzo, Salvatore Romeo, Sabrina Rossi, Angelo Paolo Dei Tos, Roberta Maestro and 1 more

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

39 citing papers in PubMed, 59 citations in OpenAlex.

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  16. Whole exome sequencing in familial isolated primary hyperparathyroidism.Journal of endocrinological investigation · 2020
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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

11 authors at 3 institutions in 1 country.

Eros Di GiorgioDipartimento di Scienze Mediche e Biologiche, Università degli Studi di Udine, Udine, Italy.
Andrea Clocchiatti
Sara Piccinin
Andrea Sgorbissa
Giulia Viviani
Paolo Peruzzo
Salvatore Romeo
Sabrina Rossi
Angelo Paolo Dei Tos
Roberta Maestro
Claudio Brancolini
University of Udine · ITCa' Foncello Hospital · ITCentro di Riferimento Oncologico · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The MEF2-class IIa histone deacetylase (HDAC) axis operates in several differentiation pathways and in numerous adaptive responses. We show here that nuclear active HDAC4 and HDAC7 display transforming capability. HDAC4 oncogenic potential depends on the repression of a limited set of genes, most of which are MEF2 targets. Genes verified as targets of the MEF2-HDAC axis are also under the influence of the phosphatidylinositol 3-kinase (PI3K)/Akt pathway that affects MEF2 protein stability. A signature of MEF2 target genes identified by this study is recurrently repressed in soft tissue sarcomas. Correlation studies depicted two distinct groups of soft tissue sarcomas: one in which MEF2 repression correlates with PTEN downregulation and a second group in which MEF2 repression correlates with HDAC4 levels. Finally, simultaneous pharmacological inhibition of the PI3K/Akt pathway and of MEF2-HDAC interaction shows additive effects on the transcription of MEF2 target genes and on sarcoma cells proliferation. Overall, our work pinpoints an important role of the MEF2-HDAC class IIa axis in tumorigenesis.

Indexed as

AnimalsCarcinogenesisCell LineCell Line, TumorCell NucleusCell ProliferationCells, CulturedCell Transformation, NeoplasticGene Expression Regulation, NeoplasticHistone DeacetylasesHumansMEF2 Transcription FactorsMiceMice, Inbred BALB CNIH 3T3 CellsPhosphatidylinositol 3-KinaseHDAC4 protein, humanHdac5 protein, mouseHDAC7 protein, humanHistone DeacetylasesMEF2 Transcription FactorsPhosphatidylinositol 3-KinaseProto-Oncogene Proteins c-aktRepressor Proteins

Identifiers

PMID24043307
PMCPMC3838174
OpenAlexW2170068929

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.