Evidence map›Paper›PMID 24657655›Full record

ArticleCancer letters2014

RUNX2 is overexpressed in melanoma cells and mediates their migration and invasion.

Rajeev K Boregowda, Oyenike O Olabisi, Walid Abushahba, Byeong-Seon Jeong, Keneshia K Haenssen, Wenjin Chen, Marina Chekmareva, Ahmed Lasfar, David J Foran, James S Goydos and 1 more

Abstract read
In one paragraph

Article in Cancer letters, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
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  4. Review
  5. Review
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  9. Article
  10. RUNX2 promotes malignant progression in gastric cancer by regulating COL1A1.Cancer biomarkers : section A of Disease markers · 2021
    Article
  11. Article
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  17. Ectopic expression of the osteogenic master geneWorld journal of stem cells · 2018
    Article
  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

11 authors at 1 institution in 1 country.

Rajeev K BoregowdaRutgers Cancer Institute of New Jersey, Department of Medicine, Division of Medical Oncology - Rutgers, The State University of New Jersey, Robert Wood Johnson Medical School, 195 Little Albany Street, New Brunswick, NJ 08903, USA.
Oyenike O OlabisiRutgers Cancer Institute of New Jersey, Department of Medicine, Division of Medical Oncology - Rutgers, The State University of New Jersey, Robert Wood Johnson Medical School, 195 Little Albany Street, New Brunswick, NJ 08903, USA.
Walid AbushahbaRutgers Cancer Institute of New Jersey, Department of Medicine, Division of Medical Oncology - Rutgers, The State University of New Jersey, Robert Wood Johnson Medical School, 195 Little Albany Street, New Brunswick, NJ 08903, USA.
Byeong-Seon JeongRutgers Cancer Institute of New Jersey, Department of Surgery, Division of Surgical Oncology, Rutgers, The State University of New Jersey, Robert Wood Johnson Medical School, 195 Little Albany Street, New Brunswick, NJ 08903, USA.
Keneshia K HaenssenRutgers Cancer Institute of New Jersey, Department of Surgery, Division of Surgical Oncology, Rutgers, The State University of New Jersey, Robert Wood Johnson Medical School, 195 Little Albany Street, New Brunswick, NJ 08903, USA.
Wenjin ChenCenter for Biomedical Imaging & Informatics - Rutgers Cancer Institute of New Jersey, 195 Little Albany Street, New Brunswick, NJ 08903, USA.
Marina ChekmarevaRutgers Cancer Institute of New Jersey - Department of Pathology and Laboratory Medicine, Robert Wood Johnson University Hospital, 1 RWJ Place, New Brunswick, NJ 08901, USA.
Ahmed LasfarDepartment of Pharmacology and Toxicology, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, 160 Frelinghuysen Road, Piscataway, NJ 08854, USA.
David J ForanCenter for Biomedical Imaging & Informatics - Rutgers Cancer Institute of New Jersey, 195 Little Albany Street, New Brunswick, NJ 08903, USA.
James S GoydosRutgers Cancer Institute of New Jersey, Department of Surgery, Division of Surgical Oncology, Rutgers, The State University of New Jersey, Robert Wood Johnson Medical School, 195 Little Albany Street, New Brunswick, NJ 08903, USA.
Karine A Cohen-SolalRutgers Cancer Institute of New Jersey, Department of Medicine, Division of Medical Oncology - Rutgers, The State University of New Jersey, Robert Wood Johnson Medical School, 195 Little Albany Street, New Brunswick, NJ 08903, USA. Electronic address: cohenska@cinj.rutgers.edu.
Rutgers, The State University of New Jersey · US

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI John Pounardjian · 1997 to 2026
$94.5M
IRACDA at Rutgers: INSPIRE Postdoctoral Training ProgramK12GM093854 · NIGMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Detlev Boison, Gary A. Brewer · 2010 to 2026
$14.7M
Image Mining for Comparative Analysis of Expression Patterns in Tissue MicroarrayR01LM009239 · NLM · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI FORAN, DAVID J, SALTZ, JOEL H. · 2007 to 2016
$4.5M
Informatics for Integrative Brain Tumor Whole Slide AnalysisR01LM011119 · NLM · STATE UNIVERSITY NEW YORK STONY BROOK · PI FORAN, DAVID J, SALTZ, JOEL H. · 2011 to 2014
$1.8M
Combination Therapy that Targets Glutamate Signaling in MelanomaR01CA149627 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI GOYDOS, JAMES S. · 2010 to 2014
$1.7M
Collaborative Systems for Analyzing Tissue MicroarraysR01CA156386 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI FORAN, DAVID J · 2010 to 2014
$1.7M
Mechano-Visual Phenotyping of Cancer: From Onset Through Disease ProgressionR01CA161375 · NCI · UNIV OF MARYLAND, COLLEGE PARK · PI DESAI, JAYDEV P., FORAN, DAVID J · 2012 to 2016
$1.6M
NCI NIH HHS 1R01CA149627-01NCI NIH HHS 5R01CA156386-08NCI NIH HHS 5R01CA161375-02NCI NIH HHS P30 CA072720NCI NIH HHS R01 CA149627NCI NIH HHS R01 CA156386NCI NIH HHS R01 CA161375NIGMS NIH HHS K12 GM093854NIGMS NIH HHS K12 GM093854-01NLM NIH HHS 5R01LM011119-03NLM NIH HHS R01 LM009239NLM NIH HHS R01 LM011119
6 · The paper itself

Abstract

In the present study, we investigated the role of the transcription factor RUNX2 in melanomagenesis. We demonstrated that the expression of transcriptionally active RUNX2 was increased in melanoma cell lines as compared with human melanocytes. Using a melanoma tissue microarray, we showed that RUNX2 levels were higher in melanoma cells as compared with nevic melanocytes. RUNX2 knockdown in melanoma cell lines significantly decreased Focal Adhesion Kinase expression, and inhibited their cell growth, migration and invasion ability. Finally, the pro-hormone cholecalciferol reduced RUNX2 transcriptional activity and decreased migration of melanoma cells, further suggesting a role of RUNX2 in melanoma cell migration.

Indexed as

Cell MovementCell Line, TumorCell ProliferationCholecalciferolCore Binding Factor Alpha 1 SubunitFocal Adhesion Kinase 1Gene Expression Regulation, NeoplasticHumansImmunohistochemistryMatrix Metalloproteinase 13MelanomaNeoplasm InvasivenessPromoter Regions, GeneticRNA InterferenceSignal TransductionSkin NeoplasmsCholecalciferolCore Binding Factor Alpha 1 SubunitFocal Adhesion Kinase 1Matrix Metalloproteinase 13PTK2 protein, humanRUNX2 protein, humanCholecalciferol (Vitamin D3)FAKMelanomaMigrationRUNX2Transcription factor

Identifiers

PMID24657655
PMCPMC4041161
OpenAlexW2018712322

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.