Evidence map›Paper›PMID 24366193›Full record

ArticleMelanoma research2014

Thrombomodulin modulates cell migration in human melanoma cell lines.

Andreia da Silva de Oliveira, Likiu Yang, Juliana Echevarria-Lima, Robson Q Monteiro, Alireza R Rezaie

Open access · greenAbstract read
In one paragraph

Article in Melanoma research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Thrombomodulin Regulates PTEN/AKT Signaling Axis in Endothelial Cells.Arteriosclerosis, thrombosis, and vascular biology · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Thrombomodulin Regulation of Mitogen-Activated Protein Kinases.International journal of molecular sciences · 2019
    Review
  8. Article
  9. Diagnostic Value of Coagulation-Fibrinolysis Biomarkers for Metastasis in Lung, Ovarian, Breast, and Colorectal Cancers.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    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

5 authors at 2 institutions in 2 countries.

Andreia da Silva de OliveiraaInstitute of Medical Biochemistry bPaulo Goés Microbiology Institute, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil cEdward A. Doisy Department of Biochemistry and Molecular Biology, St Louis University School of Medicine, St Louis, Missouri, USA.
Likiu Yang
Juliana Echevarria-Lima
Robson Q Monteiro
Alireza R Rezaie
Saint Louis University · USUniversidade Federal do Rio de Janeiro · BR

Funding

Protease Activated Receptor Signaling by Coagulation ProteasesR01HL101917 · NHLBI · SAINT LOUIS UNIVERSITY · PI Lijun Xia · 2010 to 2026
$6.6M
Serpin Regulation of Coagulation ProteasesR01HL062565 · NHLBI · SAINT LOUIS UNIVERSITY · PI REZAIE, ALIREZA R. · 1999 to 2020
$6.2M
NHLBI NIH HHS HL 101917NHLBI NIH HHS HL 62565NHLBI NIH HHS R01 HL062565NHLBI NIH HHS R01 HL101917
6 · The paper itself

Abstract

Malignant melanoma cells are known to have altered expressions of growth factors as compared with normal melanocytes. Thrombomodulin (TM) is a thrombin receptor on endothelial cells that converts thrombin from a procoagulant to an anticoagulant enzyme. TM expression is downregulated in tumor cells, and this phenomenon correlates with tumor cell invasiveness and a poor prognosis in patients with cancer. In this study, we evaluated TM expression in two human melanoma cell lines that are known to have either low (WM35) or high (A375) aggressive phenotypes. Analysis by quantitative real-time PCR (qPCR) showed that the mRNA expression of TM is modestly (WM35) or dramatically (A375) downregulated in melanoma cells, as compared with human primary melanocytes. TM expression levels inversely correlated with in-vitro migration properties of tumor cells. In addition, interleukin-8 expression also correlated with the degree of aggressiveness, as indicated by high expression levels of this cytokine in A375 cells. Overexpression of TM in A375 cells by transient transfection reversed their aggressive phenotype and dramatically decreased interleukin-8 expression by these cells. Taken together, these results suggest that downregulation of TM plays a crucial role in melanocyte transformation and melanoma progression.

Indexed as

Adenomatous Polyposis Coli ProteinAntigens, CDCell Line, TumorCell MovementDisease ProgressionDown-RegulationEndothelial Protein C ReceptorHumansInterleukin-8MelanocytesMelanomaNeoplasm InvasivenessReceptors, Cell SurfaceRNA, MessengerThrombinThrombomodulinAdenomatous Polyposis Coli ProteinAntigens, CDAPC protein, humanEndothelial Protein C ReceptorInterleukin-8PROCR protein, humanReceptors, Cell SurfaceRNA, MessengerThrombinThrombomodulinThromboplastin

Identifiers

PMID24366193
PMCPMC3874133
OpenAlexW2043517527

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.