Evidence map›Paper›PMID 24979279›Full record

ArticleOncogenesis2014

Selective CREB-dependent cyclin expression mediated by the PI3K and MAPK pathways supports glioma cell proliferation.

P Daniel, G Filiz, D V Brown, F Hollande, M Gonzales, G D'Abaco, N Papalexis, W A Phillips, J Malaterre, R G Ramsay and 1 more

Open access · goldAbstract read
In one paragraph

Article in Oncogenesis, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% 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

67 citing papers in PubMed, 1 synthesis or guideline pooled it, 110 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Journal of functional biomaterials · 2026
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  20. IL-10 in glioma.British journal of cancer · 2021
    Review

7 more citing papers are in PubMed but not listed here.

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 2 countries.

P DanielDepartment of Pathology, The University of Melbourne, Parkville, Victoria, Australia.
G FilizDepartment of Pathology, The University of Melbourne, Parkville, Victoria, Australia.
D V BrownDepartment of Pathology, The University of Melbourne, Parkville, Victoria, Australia.
F HollandeDepartment of Pathology, The University of Melbourne, Parkville, Victoria, Australia.
M Gonzales1] Department of Pathology, The University of Melbourne, Parkville, Victoria, Australia [2] Department of Anatomical Pathology, The Royal Melbourne Hospital, Parkville, Victoria, Australia.
G D'AbacoNICTA Victorian Research Laboratories, Centre for Neural Engineering, The University of Melbourne, Carlton, Australia.
N PapalexisLaboratory of Physiology, Faculty of Medicine, University of Patras, Patras, Greece.
W A Phillips1] Surgical Oncology Research Laboratory, Peter MacCullum Cancer Centre, Melbourne, Victoria, Australia [2] Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, Victoria, Australia.
J Malaterre1] Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, Victoria, Australia [2] Differentiation and Transcription Laboratory, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
R G Ramsay1] Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, Victoria, Australia [2] Differentiation and Transcription Laboratory, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
T Mantamadiotis1] Department of Pathology, The University of Melbourne, Parkville, Victoria, Australia [2] Laboratory of Physiology, Faculty of Medicine, University of Patras, Patras, Greece.
University of Melbourne · AUPeter MacCallum Cancer Centre · AUUniversity of Patras · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cyclic-AMP response element binding (CREB) protein has been shown to have a pivotal role in cell survival and cell proliferation. Transgenic rodent models have revealed a role for CREB in higher-order brain functions, such as memory and drug addiction behaviors. CREB overexpression in transgenic animals imparts oncogenic properties on cells in various tissues, and aberrant CREB expression is associated with tumours. It is the central position of CREB, downstream from key developmental and growth signalling pathways, which gives CREB this ability to influence a spectrum of cellular activities, such as cell survival, growth and differentiation, in both normal and cancer cells. We show that CREB is highly expressed and constitutively activated in patient glioma tissue and that this activation closely correlates with tumour grade. The mechanism by which CREB regulates glioblastoma (GBM) tumour cell proliferation involves activities downstream from both the mitogen-activated protein kinase and phosphoinositide 3-kinase (PI3K) pathways that then modulate the expression of three key cell cycle factors, cyclin B, D and proliferating cell nuclear antigen (PCNA). Cyclin D1 is highly CREB-dependent, whereas cyclin B1 and PCNA are co-regulated by both CREB-dependent and -independent mechanisms. The precise regulatory network involved appears to differ depending on the tumour-suppressor phosphatase and tensin homolog status of the GBM cells, which in turn allows CREB to regulate the activity of the PI3K itself. Given that CREB sits at the hub of key cancer cell signalling pathways, understanding the role of glioma-specific CREB function may lead to improved novel combinatorial anti-tumour therapies, which can complement existing PI3K-specific drugs undergoing early phase clinical trials.

Identifiers

PMID24979279
PMCPMC4150215
OpenAlexW2061586485

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.