Evidence map›Paper›PMID 24479521›Full record

ArticleBreast cancer research : BCR2014

Runx2 activates PI3K/Akt signaling via mTORC2 regulation in invasive breast cancer cells.

Manish Tandon, Zujian Chen, Jitesh Pratap

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.9field-weighted citation impact, top 3% 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

44 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. RUNX2 promotes malignant progression in gastric cancer by regulating COL1A1.Cancer biomarkers : section A of Disease markers · 2021
    Article
  18. Article
  19. 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

3 authors at 1 institution in 1 country.

Manish Tandon
Zujian Chen
Jitesh Pratap
Rush University Medical Center · US

Funding

Recruitment of a Bone and Cancer Early Stage InvestigatorP30CA147881 · NCI · RUSH UNIVERSITY MEDICAL CENTER · PI SUMNER, D RICK · 2009 to 2010
$775k
NCI NIH HHS 5P30CA147881
6 · The paper itself

Abstract

introductionThe Runt-related transcription factor Runx2 is critical for skeletal development but is also aberrantly expressed in breast cancers, and promotes cell growth and invasion. A de-regulated serine/threonine kinase Akt signaling pathway is implicated in mammary carcinogenesis and cell survival; however, the mechanisms underlying Runx2 role in survival of invasive breast cancer cells are still unclear.

methodsThe phenotypic analysis of Runx2 function in cell survival was performed by gene silencing and flow cytometric analysis in highly invasive MDA-MB-231 and SUM-159-PT mammary epithelial cell lines. The expression analysis of Runx2 and pAkt (serine 473) proteins in metastatic breast cancer specimens was performed by immunohistochemistry. The mRNA and protein levels of kinases and phosphatases functional in Akt signaling were determined by real-time PCR and Western blotting, while DNA-protein interaction was studied by chromatin immunoprecipitation assays.

resultsThe high Runx2 levels in invasive mammary epithelial cell lines promoted cell survival in Akt phosphorylation (pAkt-serine 473) dependent manner. The analysis of kinases and phosphatases associated with pAkt regulation revealed that Runx2 promotes pAkt levels via mammalian target of rapamycin complex-2 (mTORC2). The recruitment of Runx2 on mTOR promoter coupled with Runx2-dependent expression of mTORC2 component Rictor defined Runx2 function in pAkt-mediated survival of invasive breast cancer cells.

conclusionsOur results identified a novel mechanism of Runx2 regulatory crosstalk in Akt signaling that could have important consequences in targeting invasive breast cancer-associated cell survival.

Indexed as

ApoptosisBreast NeoplasmsCell Line, TumorCell ProliferationCell SurvivalChromonesCore Binding Factor Alpha 1 SubunitExtracellular Signal-Regulated MAP KinasesFemaleHumansMCF-7 CellsMechanistic Target of Rapamycin Complex 2MorpholinesMultiprotein ComplexesNeoplasm InvasivenessNuclear Proteins2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-oneChromonesCore Binding Factor Alpha 1 SubunitExtracellular Signal-Regulated MAP KinasesMechanistic Target of Rapamycin Complex 2MorpholinesMultiprotein ComplexesNuclear ProteinsPHLPP1 protein, humanPhosphatidylinositol 3-KinasePhosphoinositide-3 Kinase InhibitorsPhosphoprotein PhosphatasesProto-Oncogene Proteins c-aktRNA, Small InterferingRUNX2 protein, humanTOR Serine-Threonine Kinases

Identifiers

PMID24479521
PMCPMC3979058
OpenAlexW2114446881

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.