Evidence map›Paper›PMID 19657062›Full record

ArticleAmerican journal of physiology. Cell physiology2009

Epac increases melanoma cell migration by a heparan sulfate-related mechanism.

Erdene Baljinnyam, Kousaku Iwatsubo, Reiko Kurotani, Xu Wang, Coskun Ulucan, Mizuka Iwatsubo, David Lagunoff, Yoshihiro Ishikawa

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2009. 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
2.1field-weighted citation impact, top 14% 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, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. The Role of Epac in Cancer Progression.International journal of molecular sciences · 2020
    Review
  9. Review
  10. Lung Adenocarcinoma Syndecan-2 Potentiates Cell Invasiveness.American journal of respiratory cell and molecular biology · 2019
    Article
  11. Article
  12. Article
  13. Review
  14. Cancer Cell Glycocalyx and Its Significance in Cancer Progression.International journal of molecular sciences · 2018
    Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Erdene BaljinnyamDepartment of Cell Biology and Molecular Medicine, New Jersey Medical School-University of Medicine and Dentistry of New Jersey, Newark, New Jersey, USA.
Kousaku Iwatsubo
Reiko Kurotani
Xu Wang
Coskun Ulucan
Mizuka Iwatsubo
David Lagunoff
Yoshihiro Ishikawa
Institute of Molecular and Cell Biology · RURutgers New Jersey Medical SchoolYokohama City University · JP

Funding

SARCOMERIC PROTEIN MUTATIONS IN HYPERTROPHY AND HEART FAILUREP01HL059139 · NHLBI · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI RYDEN, EVA B · 1997 to 2007
$12.4M
Catalytic activation of adenylyl cyclase type VR01GM067773 · NIGMS · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI ISHIKAWA, YOSHIHIRO · 2004 to 2007
$1.3M
NHLBI NIH HHS HL-059139NIGMS NIH HHS GM-067773
6 · The paper itself

Abstract

Melanoma, the most malignant form of human skin cancer, has a poor prognosis due to its strong metastatic ability. It was recently demonstrated that Epac, an effector molecule of cAMP, is involved in regulating cell migration; however, the role of Epac in melanoma cell migration remains unclear. We thus examined whether Epac regulates cell migration and metastasis of melanoma. Epac activation, by either specific agonist or overexpression of Epac, increased melanoma cell migration. Deletion of endogenous Epac with small interfering RNA decreased basal melanoma cell migration. These data suggested a major role of Epac in melanoma cell migration. Epac-induced cell migration was mediated by translocation of syndecan-2, a cell-surface heparan sulfate proteoglycan, to lipid rafts. This syndecan-2 translocation was regulated by tubulin polymerization via the Epac/phosphoinositol-3 kinase pathway. Epac-induced cell migration was also regulated by the production of heparan sulfate, a major extracellular matrix. Epac-induced heparan sulfate production was attributable to the increased expression of N-deacetylase/N-sulfotransferase-1 (NDST-1) accompanied by an increased NDST-1 translation rate. Finally, Epac overexpression enhanced lung colonization of melanoma cells in mice. Taken together, these data indicate that Epac regulates melanoma cell migration/metastasis mostly via syndecan-2 translocation and heparan sulfate production.

Indexed as

AnimalsCell Line, TumorCell MovementGuanine Nucleotide Exchange FactorsHeparan SulfateHumansMelanomaMelanoma, ExperimentalMiceMice, NudeNeoplasm InvasivenessNeoplasm TransplantationPhosphatidylinositol 3-KinasesProtein TransportSignal TransductionSulfotransferasesGuanine Nucleotide Exchange FactorsHeparan Sulfateheparitin sulfotransferasePhosphatidylinositol 3-KinasesRAPGEF3 protein, humanSulfotransferasesSyndecan-2Tubulin

Identifiers

PMID19657062
PMCPMC2770742
OpenAlexW2018252424

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.