Evidence map›Paper›PMID 21593193›Full record

ArticleCancer research2011

A novel function of junctional adhesion molecule-C in mediating melanoma cell metastasis.

Harald F Langer, Valeria V Orlova, Changping Xie, Sunil Kaul, Darius Schneider, Anke S Lonsdorf, Manuela Fahrleitner, Eun Young Choi, Vanessa Dutoit, Manuela Pellegrini and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.0field-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

39 citing papers in PubMed, 88 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Junctional adhesion molecule-C: A multifunctional mediator of cell adhesion.Cellular and molecular life sciences : CMLS · 2025
    Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Cancer-associated fibroblasts in colorectal cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  12. Article
  13. Article
  14. The Roles of Junctional Adhesion Molecules (JAMs) in Cell Migration.Frontiers in cell and developmental biology · 2022
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  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

17 authors at 6 institutions in 3 countries.

Harald F LangerExperimental Immunology Branch, National Cancer Institute, NIH, Bethesda, Maryland, USA.
Valeria V Orlova
Changping Xie
Sunil Kaul
Darius Schneider
Anke S Lonsdorf
Manuela Fahrleitner
Eun Young Choi
Vanessa Dutoit
Manuela Pellegrini
Sylvia Grossklaus
Peter P Nawroth
Gustavo Baretton
Sentot Santoso
Sam T Hwang
Bernd Arnold
Triantafyllos Chavakis
Heidelberg University · DEGerman Cancer Research Center · DELeiden University Medical Center · NLNational Cancer Institute · USMedical College of Wisconsin · USUniversity Hospital Heidelberg · DE

Funding

Application of Flow Cytometry to Cell BiologyZICBC009255 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CROSSMAN, ASSIATU · 2009 to 2025
$26.4M
The role of junctional adhesion molecule-C (JAM-C) in adZ01BC010663 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CHAVAKIS, TRIANTAFYLLOS · 2005 to 2008
$674k
The Role of JAM-C in Adhesive Interactions of Immune CellsZIABC010663 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CHAVAKIS, TRIANTAFYLLOS · 2009 to 2010
$592k
Intramural NIH HHS Z01 BC010663Intramural NIH HHS ZIA BC010663
6 · The paper itself

Abstract

Hematogenous dissemination of melanoma is a life-threatening complication of this malignant tumor. Here, we identified junctional adhesion molecule-C (JAM-C) as a novel player in melanoma metastasis to the lung. JAM-C expression was identified in human and murine melanoma cell lines, in human malignant melanoma, as well as in metastatic melanoma including melanoma lung metastasis. JAM-C expressed on both murine B16 melanoma cells as well as on endothelial cells promoted the transendothelial migration of the melanoma cells. We generated mice with inactivation of JAM-C. JAM-C(-/-) mice as well as endothelial-specific JAM-C-deficient mice displayed significantly decreased B16 melanoma cell metastasis to the lung, whereas treatment of mice with soluble JAM-C prevented melanoma lung metastasis. Together, JAM-C represents a novel therapeutic target for melanoma metastasis.

Indexed as

AnimalsCell Adhesion MoleculesCell Line, TumorCell MovementCHO CellsCricetinaeCricetulusEndothelial CellsHumansImmunoglobulinsLung NeoplasmsMelanomaMiceMice, Inbred C57BLNeoplasm InvasivenessCell Adhesion MoleculesImmunoglobulinsJAM3 protein, humanJam3 protein, mouse

Identifiers

PMID21593193
PMCPMC3117056
OpenAlexW2159897971

What OpenQuestion holds

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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.