Evidence map›Paper›PMID 18223689›Full record

ArticleOncogene2008

Runx2-mediated activation of the Bax gene increases osteosarcoma cell sensitivity to apoptosis.

R A Eliseev, Y-F Dong, E Sampson, M J Zuscik, E M Schwarz, R J O'Keefe, R N Rosier, M H Drissi

Abstract read
In one paragraph

Article in Oncogene, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
–field-weighted citation impact
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

43 citing papers in PubMed.

  1. Review
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  13. Chondrocyte-Specific RUNX2 Overexpression Accelerates Post-traumatic Osteoarthritis Progression in Adult Mice.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2019
    Article
  14. Article
  15. OncoTargets and therapy · 2018
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

8 authors.

R A EliseevDepartment of Orthopaedics, Center for Musculoskeletal Research, University of Rochester Medical Center, Rochester, NY, USA.
Y-F Dong
E Sampson
M J Zuscik
E M Schwarz
R J O'Keefe
R N Rosier
M H Drissi

Funding

Runx-mediated regulation of endochondral ossificationR01AR052674 · NIAMS · UNIVERSITY OF ROCHESTER · PI DRISSI, MOULAY HICHAM · 2005 to 2008
$1.0M
NIAMS NIH HHS R01 AR052674NIAMS NIH HHS R0-1 AR-052674-01
6 · The paper itself

Abstract

The Runx family of transcription factors regulate cell growth and differentiation, and control the expression of target genes involved in cell fate decisions. We examined the role of the bone-related member of this family, Runx2, in regulating apoptosis via modulation of the Bcl2 family of genes in the osteosarcoma cell line Saos2. Our data demonstrate that Runx2 directly binds to two Runx-specific regulatory elements on the human bax promoter thereby inducing Bax expression. Furthermore, bone morphogenetic protein-induced or vector-mediated expression of Runx2 resulted in upregulation of Bax expression, and subsequent increased sensitivity of Saos2 cells to apoptosis. Finally, the observed upregulation of Bax expression and increased apoptosis were Runx2 dependent as Runx2 loss of function abrogated these effects. Our study provides the first evidence for Bax as a direct target of Runx2, suggesting that Runx2 may act as a proapoptotic factor in osteosarcoma cells.

Indexed as

ApoptosisGene Expression Regulation, Neoplasticbcl-2-Associated X ProteinBone NeoplasmsCaspase 3Cell Line, TumorCore Binding Factor Alpha 1 SubunitGene Expression RegulationHumansModels, BiologicalMutagenesis, Site-DirectedOsteosarcomaPromoter Regions, GeneticTranscriptional Activationbcl-2-Associated X ProteinCaspase 3Core Binding Factor Alpha 1 SubunitRUNX2 protein, human

Identifiers

PMID18223689
PMCPMC6247425

What OpenQuestion holds

Textmetadata
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.