Evidence map›Paper›PMID 22052333›Full record

ArticleJournal of neuro-oncology2012

Growth inhibition of malignant glioblastoma by DING protein.

Markus J Bookland, Nune Darbinian, Michael Weaver, Shohreh Amini, Kamel Khalili

Abstract read
In one paragraph

Article in Journal of neuro-oncology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. DING Proteins Extend to the Extremophilic World.International journal of molecular sciences · 2021
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. DING proteins: numerous functions, elusive genes, a potential for health.Cellular and molecular life sciences : CMLS · 2013
    Review
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

5 authors at 2 institutions in 1 country.

Markus J BooklandDepartment of Neuroscience, Center for Neurovirology, Temple University School of Medicine, Room 741 MERB, 3500 North Broad St., Philadelphia, PA 19140, USA.
Nune Darbinian
Michael Weaver
Shohreh Amini
Kamel Khalili
Temple University · USTemple College · US

Funding

TAT induced deregulation of neuronal differentiation and survival by NGFP01NS043980 · NINDS · TEMPLE UNIV OF THE COMMONWEALTH · PI REISS, KRZYSZTOF · 2002 to 2012
$11.5M
Suppression of HIV-1 in CNS by a novel protein from ST John's WortR01MH074392 · NIMH · TEMPLE UNIV OF THE COMMONWEALTH · PI AMINI, SHOHREH · 2006 to 2010
$1.6M
NIMH NIH HHS R01 MH074392NINDS NIH HHS P01 NS043980
6 · The paper itself

Abstract

Malignant gliomas are a highly aggressive type of brain tumor with extremely poor prognosis. These tumors are highly invasive and are often surgically incurable and resistant to chemotherapeutics and radiotherapy. Thus, novel therapies that target pathways involved in growth and survival of the tumor cells are required for the treatment of this class of brain tumors. Previous studies revealed that epidermal growth factor receptor and extracellular-signal-regulated kinases (ERKs), which are involved in the induction of cell proliferation, are activated in the most aggressive type of glioma, i.e. glioblastoma multiforme (GBM). In fact, GBMs with increased levels of ERK activity exhibit a more aggressive phenotype than the others with moderate ERK activity, pointing to the importance of ERK and its kinase activity in the development and progression of these tumors. In this study, we have evaluated the effect of p38SJ, a novel member of the DING family of proteins, derived from Hypericum perforatum calluses, on the growth of malignant glioma cell lines, T98G and U-87MG by focusing on cell cycle and signaling pathways controlled by phosphorylation of various regulatory proteins including ERK. p38SJ, which exhibits profound phosphatase activity, shows the capacity to affect the phosphorylation status of several important kinases modulating signaling pathways, and cell growth and proliferation. Our results demonstrate that p38SJ reduces glioma cell viability and arrests cell cycle progression at G0/G1. The observed growth inhibitory effect of p38SJ is likely mediated by the downregulation of several cell cycle gatekeeper proteins, including cyclin E, Cdc2, and E2F-1. These results suggest that p38SJ may serve as a potential candidate for development of a therapeutic agent for the direct treatment of malignant gliomas and/or as a potential radiosensitizer.

Indexed as

AnimalsCDC2 Protein KinaseCell Cycle CheckpointsCell Line, TransformedCell Line, TumorCell ProliferationCyclin BCyclin-Dependent KinasesCyclin EDNA-Binding ProteinsE2F Transcription FactorsEndopeptidase KExtracellular Signal-Regulated MAP KinasesFlow CytometryGene Expression Regulation, NeoplasticGlioblastomaCDC2 Protein KinaseCDK1 protein, humanCyclin BCyclin-Dependent KinasesCyclin EDNA-Binding ProteinsE2F Transcription FactorsEndopeptidase Kenhanced green fluorescent proteinExtracellular Signal-Regulated MAP KinasesGreen Fluorescent ProteinsPlant PreparationsPolycomb Repressive Complex 1RNF2 protein, humanTetrazolium SaltsThiazolesthiazolyl blueUbiquitin-Protein Ligases

Identifiers

PMID22052333
PMCPMC4631253
OpenAlexW2074959789

What OpenQuestion holds

Textmetadata
LicenceTDM
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.