Evidence map›Paper›PMID 29932116›Full record

ReviewInternational journal of molecular sciences2018

Targeting mTOR as a Therapeutic Approach in Medulloblastoma.

Juncal Aldaregia, Ainitze Odriozola, Ander Matheu, Idoia Garcia

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. 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
0.8field-weighted citation impact, top 28% 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, 17 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Medulloblastoma in the Modern Era: Review of Contemporary Trials, Molecular Advances, and Updates in Management.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
    Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. mTOR in Human Diseases.International journal of molecular sciences · 2019
    Article
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

4 authors at 2 institutions in 1 country.

Juncal AldaregiaCellular Oncology Group, Biodonostia Research Institute, 20014 Donostia-San Sebastián, Spain. juncal.aldareguia@biodonostia.org.
Ainitze OdriozolaCellular Oncology Group, Biodonostia Research Institute, 20014 Donostia-San Sebastián, Spain. ainitzeodri15@gmail.com.
Ander MatheuCellular Oncology Group, Biodonostia Research Institute, 20014 Donostia-San Sebastián, Spain. ander.matheu@biodonostia.org.
Idoia GarciaCellular Oncology Group, Biodonostia Research Institute, 20014 Donostia-San Sebastián, Spain. idoia.garcia@biodonostia.org.
Biogipuzkoa Health Research Institute · ESUniversity of the Basque Country · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mechanistic target of rapamycin (mTOR) is a master signaling pathway that regulates organismal growth and homeostasis, because of its implication in protein and lipid synthesis, and in the control of the cell cycle and the cellular metabolism. Moreover, it is necessary in cerebellar development and stem cell pluripotency maintenance. Its deregulation has been implicated in the medulloblastoma and in medulloblastoma stem cells (MBSCs). Medulloblastoma is the most common malignant solid tumor in childhood. The current therapies have improved the overall survival but they carry serious side effects, such as permanent neurological sequelae and disability. Recent studies have given rise to a new molecular classification of the subgroups of medulloblastoma, specifying 12 different subtypes containing novel potential therapeutic targets. In this review we propose the targeting of mTOR, in combination with current therapies, as a promising novel therapeutic approach.

Indexed as

AnimalsBridged Bicyclo Compounds, HeterocyclicCerebellar NeoplasmsHumansMedulloblastomaMolecular Targeted TherapyMorpholinesProtein Kinase InhibitorsPyrimidinesSignal TransductionTOR Serine-Threonine KinasesTriazines1-(4-((2-(2-aminopyrimidin-5-yl)-7-methyl-4-morpholinothieno(3,2-d)pyrimidin-6-yl)methyl)piperazin-1-yl)-2-hydroxypropan-1-oneBridged Bicyclo Compounds, HeterocyclicgedatolisibMorpholinesMTOR protein, humanProtein Kinase InhibitorsPyrimidinesTOR Serine-Threonine KinasesTriazinesMBSCsMedulloblastomamTOR

Identifiers

PMID29932116
PMCPMC6073374
OpenAlexW2808783721

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.