Evidence map›Paper›PMID 27067975›Full record

ArticleThrombosis research2016

Activated tumor cell integrin αvβ3 cooperates with platelets to promote extravasation and metastasis from the blood stream.

Martin R Weber, Masahiko Zuka, Mihaela Lorger, Mario Tschan, Bruce E Torbett, Andries Zijlstra, James P Quigley, Karin Staflin, Brian P Eliceiri, Joseph S Krueger and 3 more

Abstract read
In one paragraph

Article in Thrombosis research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
7.3field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

  1. Pooled it
  2. Immunotherapeutic Strategies Targeting GD2-Expressing Malignancies.Advances in experimental medicine and biology · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Targeting the αVβ3/NgR2 pathway in neuroendocrine prostate cancer.Matrix biology : journal of the International Society for Matrix Biology · 2023
    Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  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

13 authors at 2 institutions in 1 country.

Martin R WeberDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California, USA.
Masahiko ZukaDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California, USA.
Mihaela LorgerDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California, USA.
Mario TschanDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California, USA.
Bruce E TorbettDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California, USA.
Andries ZijlstraDepartment of Cell Biology, The Scripps Research Institute, La Jolla, California, USA.
James P QuigleyDepartment of Cell Biology, The Scripps Research Institute, La Jolla, California, USA.
Karin StaflinDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California, USA.
Brian P EliceiriDepartment of Surgery, University of California San Diego, San Diego, CA 92103, USA.
Joseph S KruegerDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California, USA.
Patrizia MarcheseDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California, USA.
Zaverio M RuggeriDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California, USA.
Brunhilde H FeldingDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California, USA; Department of Chemical Physiology, The Scripps Research Institute, La Jolla, California, USA. Electronic address: brunie@scripps.edu.
Scripps Research Institute · USUniversity of California, San Diego · US

Funding

Transmembrane Proteins Involved in Human Tumor ExpansionR01CA105412 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI QUIGLEY, JAMES P · 2004 to 2020
$5.8M
Normalizing Breast Cancer Metabolism to Prevent Progression and Recurrence (PQ21)R01CA170737 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI FELDING, BRUNIE H. · 2012 to 2015
$2.1M
Role of Inflammatory Neutrophils and their Unique MMP-9 in Tumor ProgressionR01CA157792 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI DERYUGINA, ELENA I · 2012 to 2016
$1.9M
Vascular mechanisms regulating breast cancer brain metastasisR01CA170140 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ELICEIRI, BRIAN P, FELDING, BRUNIE H. · 2012 to 2016
$1.8M
Antibody Fingerprinting of Triple Negative Breast Cancer by High Throughput FACSR21CA198595 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI FELDING, BRUNIE H., SMIDER, VAUGHN VASIL · 2015 to 2016
$457k
NCI NIH HHS R01 CA105412NCI NIH HHS R01 CA157792NCI NIH HHS R01 CA170140NCI NIH HHS R01CA170140NCI NIH HHS R01 CA170737NCI NIH HHS R01CA170737NCI NIH HHS R21 CA198595NCI NIH HHS R21CA198595
6 · The paper itself

Abstract

Metastasis is the main cause of death in cancer patients, and understanding mechanisms that control tumor cell dissemination may lead to improved therapy. Tumor cell adhesion receptors contribute to cancer spreading. We noted earlier that tumor cells can expressing the adhesion receptor integrin αvβ3 in distinct states of activation, and found that cells which metastasize from the blood stream express it in a constitutively high affinity form. Here, we analyzed steps of the metastatic cascade in vivo and asked, when and how the affinity state of integrin αvβ3 confers a critical advantage to cancer spreading. Following tumor cells by real time PCR, non-invasive bioluminescence imaging, intravital microscopy and histology allowed us to identify tumor cell extravasation from the blood stream as a rate-limiting step supported by high affinity αvβ3. Successful transendothelial migration depended on cooperation between tumor cells and platelets involving the high affinity tumor cell integrin and release of platelet granules. Thus, this study identifies the high affinity conformer of integrin αvβ3 and its interaction with platelets as critical for early steps during hematogenous metastasis and target for prevention of metastatic disease.

Indexed as

AnimalsBlood PlateletsCell Line, TumorCell MovementHumansIntegrin alphaVbeta3Mice, SCIDNeoplasm MetastasisNeoplastic Cells, CirculatingIntegrin alphaVbeta3Blood streamExtravasationIntegrin activationMetastasisPlatelets

Identifiers

PMID27067975
PMCPMC4888909
OpenAlexW2335037156

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.