Evidence map›Paper›PMID 24346283›Full record

ArticleBritish journal of cancer2014

Epigenetic silencing of miRNA-9 is associated with HES1 oncogenic activity and poor prognosis of medulloblastoma.

G Fiaschetti, L Abela, N Nonoguchi, A M Dubuc, M Remke, A Boro, E Grunder, U Siler, H Ohgaki, M D Taylor and 3 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

33 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. The Non-coding Side of Medulloblastoma.Frontiers in cell and developmental biology · 2020
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. The clinicopathological significance ofOncoTargets and therapy · 2017
    Article
  19. miR-137 plays tumor suppressor roles in gastric cancer cell lines by targeting KLF12 and MYO1C.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  20. 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

13 authors at 2 institutions in 1 country.

G FiaschettiNeuro-Oncology group, Experimental Infectious Diseases and Cancer Research, August-Forel Strasse 1, Zurich CH-8008, Switzerland.
L AbelaDivision of Oncology, University Children's Hospital of Zürich, Steinwiesstrasse 75, Zurich CH-8032, Switzerland.
N NonoguchiInternational Agency for Research on Cancer, World Health Organization, Section of Molecular Pathology, 150 Cours Albert Thomas, 69372, Lyon Cedex 08, France.
A M DubucArthur and Sonia Labatt Brain Tumour Research Centre, MaRS Centre - 11-401M, 101 College Street, Toronto, ON M5G1L7, Canada.
M RemkeBrain Tumor Research Centre, 101 College Street, TMDT-11-401M, Toronto, ON M5G1L7, Canada.
A BoroOncology group, Experimental Infectious Diseases and Cancer Research, August-Forel Strasse 1, Zurich CH-8008, Switzerland.
E GrunderDivision of Oncology, University Children's Hospital of Zürich, Steinwiesstrasse 75, Zurich CH-8032, Switzerland.
U SilerDivision of Immunology, University Children's Hospital of Zürich, Steinwiesstrasse 75, Zurich CH-8032, Switzerland.
H OhgakiInternational Agency for Research on Cancer, World Health Organization, Section of Molecular Pathology, 150 Cours Albert Thomas, 69372, Lyon Cedex 08, France.
M D TaylorThe Hospital for Sick Children, Division of Neurosurgery, Suite 1504, 555 University Avenue, Toronto, ON M5G1X8, Canada.
M BaumgartnerNeuro-Oncology group, Experimental Infectious Diseases and Cancer Research, August-Forel Strasse 1, Zurich CH-8008, Switzerland.
T ShalabyNeuro-Oncology group, Experimental Infectious Diseases and Cancer Research, August-Forel Strasse 1, Zurich CH-8008, Switzerland.
M A GrotzerDivision of Oncology, University Children's Hospital of Zürich, Steinwiesstrasse 75, Zurich CH-8032, Switzerland.
Hospital for Sick Children · CAOccupational Cancer Research Centre · CA

Funding

World Health Organization 001
6 · The paper itself

Abstract

backgroundmicroRNA-9 is a key regulator of neuronal development aberrantly expressed in brain malignancies, including medulloblastoma. The mechanisms by which microRNA-9 contributes to medulloblastoma pathogenesis remain unclear, and factors that regulate this process have not been delineated.

methodsExpression and methylation status of microRNA-9 in medulloblastoma cell lines and primary samples were analysed. The association of microRNA-9 expression with medulloblastoma patients' clinical outcome was assessed, and the impact of microRNA-9 restoration was functionally validated in medulloblastoma cells.

resultsmicroRNA-9 expression is repressed in a large subset of MB samples compared with normal fetal cerebellum. Low microRNA-9 expression correlates significantly with the diagnosis of unfavourable histopathological variants and with poor clinical outcome. microRNA-9 silencing occurs via cancer-specific CpG island hypermethylation. HES1 was identified as a direct target of microRNA-9 in medulloblastoma, and restoration of microRNA-9 was shown to trigger cell cycle arrest, to inhibit clonal growth and to promote medulloblastoma cell differentiation.

conclusionsmicroRNA-9 is a methylation-silenced tumour suppressor that could be a potential candidate predictive marker for poor prognosis of medulloblastoma. Loss of microRNA-9 may confer a proliferative advantage to tumour cells, and it could possibly contribute to disease pathogenesis. Thus, re-expression of microRNA-9 may constitute a novel epigenetic regulation strategy against medulloblastoma.

Indexed as

Epigenesis, GeneticAdultAgedBasic Helix-Loop-Helix ProteinsBrain NeoplasmsCell DifferentiationCell Line, TumorCell ProliferationCerebellumCpG IslandsFemaleFetusGene SilencingHomeodomain ProteinsHumansMaleBasic Helix-Loop-Helix ProteinsHES1 protein, humanHomeodomain ProteinsMicroRNAsTranscription Factor HES-1

Identifiers

PMID24346283
PMCPMC3915127
OpenAlexW2042593536

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.