Evidence map›Paper›PMID 26036258›Full record

ArticleOncotarget2015

The SIRT1/TP53 axis is activated upon B-cell receptor triggering via miR-132 up-regulation in chronic lymphocytic leukemia cells.

Michele Dal Bo, Tiziana D'Agaro, Stefania Gobessi, Antonella Zucchetto, Sara Dereani, Davide Rossi, Francesco Zaja, Gabriele Pozzato, Francesco Di Raimondo, Gianluca Gaidano and 5 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Review
  7. Role of SIRT1 in hematologic malignancies.Journal of Zhejiang University. Science. B · 2019
    Review
  8. Article
  9. Article
  10. Article
  11. 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

15 authors at 8 institutions in 1 country.

Michele Dal BoClinical and Experimental Onco-Hematology Unit, Centro di Riferimento Oncologico, I.R.C.C.S., Aviano, Pordenone, Italy.
Tiziana D'AgaroClinical and Experimental Onco-Hematology Unit, Centro di Riferimento Oncologico, I.R.C.C.S., Aviano, Pordenone, Italy.
Stefania GobessiMolecular Hematology, International Centre for Genetic Engineering and Biotechnology, Rome, Italy.
Antonella ZucchettoClinical and Experimental Onco-Hematology Unit, Centro di Riferimento Oncologico, I.R.C.C.S., Aviano, Pordenone, Italy.
Sara DereaniClinical and Experimental Onco-Hematology Unit, Centro di Riferimento Oncologico, I.R.C.C.S., Aviano, Pordenone, Italy.
Davide RossiDivision of Hematology, Department of Clinical and Experimental Medicine, Amedeo Avogadro University of Eastern Piedmont, Novara, Italy.
Francesco ZajaClinica Ematologica, Centro Trapianti e Terapie Cellulari "Carlo Melzi" DISM, Azienda Ospedaliera Universitaria S. Maria Misericordia, Udine, Italy.
Gabriele PozzatoDepartment of Internal Medicine and Hematology, Maggiore General Hospital, University of Trieste, Trieste, Italy.
Francesco Di RaimondoDivision of Hematology, Ferrarotto Hospital, Catania, Italy.
Gianluca GaidanoDivision of Hematology, Department of Clinical and Experimental Medicine, Amedeo Avogadro University of Eastern Piedmont, Novara, Italy.
Luca LaurentiDepartment of Hematology, Catholic University Hospital A. Gemelli, Rome, Italy.
Giovanni Del PoetaDivision of Hematology, S. Eugenio Hospital and University of Tor Vergata, Rome, Italy.
Dimitar G EfremovMolecular Hematology, International Centre for Genetic Engineering and Biotechnology, Rome, Italy.
Valter GatteiClinical and Experimental Onco-Hematology Unit, Centro di Riferimento Oncologico, I.R.C.C.S., Aviano, Pordenone, Italy.
Riccardo BombenClinical and Experimental Onco-Hematology Unit, Centro di Riferimento Oncologico, I.R.C.C.S., Aviano, Pordenone, Italy.
Centro di Riferimento Oncologico · ITInternational Centre for Genetic Engineering and Biotechnology · ITUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITAgostino Gemelli University Polyclinic · ITAzienda Ospedaliera S.Maria · ITFerrarotto Hospital · ITSt. Eugenio Hospital · ITUniversity of Trieste · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The B-cell receptor (BCR) plays an important role in the pathogenesis and progression of chronic lymphocytic leukemia (CLL). By global microRNA profiling of CLL cells stimulated or not stimulated by anti-IgM, significant up-regulation of microRNAs from the miR-132~212 cluster was observed both in IGHV gene unmutated (UM) and mutated (M) CLL cells. Parallel gene expression profiling identified SIRT1, a deacetylase targeting several proteins including TP53, among the top-ranked miR-132 target genes down-regulated upon anti-IgM exposure. The direct regulation of SIRT1 expression by miR-132 was demonstrated using luciferase assays. The reduction of SIRT1 mRNA and protein (P = 0.001) upon anti-IgM stimulation was associated with an increase in TP53 acetylation (P = 0.007), and the parallel up-regulation of the TP53 target gene CDKN1A. Consistently, miR-132 transfections of CLL-like cells resulted in down-regulation of SIRT1 and an induction of a TP53-dependent apoptosis. Finally, in a series of 134 CLL samples, miR-132, when expressed above the median value, associated with prolonged time-to-first-treatment in patients with M CLL (HR = 0.41; P = 0.02). Collectively, the miR-132/SIRT1/TP53 axis was identified as a novel pathway triggered by BCR engagement that further increases the complexity of the interactions between tumor microenvironments and CLL cells.

Indexed as

B-LymphocytesCase-Control StudiesCell ProliferationGenes, p53HumansLeukemia, Lymphocytic, Chronic, B-CellMicroRNAsReceptors, Antigen, B-CellSignal TransductionSirtuin 1TransfectionTumor Cells, CulturedTumor Suppressor Protein p53Up-RegulationMicroRNAsMIRN132 microRNA, humanReceptors, Antigen, B-CellSIRT1 protein, humanSirtuin 1TP53 protein, humanTumor Suppressor Protein p53BCRCLLmiR-132

Identifiers

PMID26036258
PMCPMC4662478
OpenAlexW1942842744

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.