Evidence map›Paper›PMID 21301066›Full record

ArticlePhysical biology2011

Promotion of experimental thrombus formation by the procoagulant activity of breast cancer cells.

M A Berny-Lang, J E Aslan, G W Tormoen, I A Patel, P E Bock, A Gruber, O J T McCarty

Abstract read
In one paragraph

Article in Physical biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. The role of coagulation and platelets in colon cancer-associated thrombosis.American journal of physiology. Cell physiology · 2019
    Article
  5. Article
  6. Article
  7. Physical biology in cancer. 2. The physical biology of circulating tumor cells.American journal of physiology. Cell physiology · 2014
    Review
  8. Review
  9. Review
  10. Article
  11. Article
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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

7 authors at 2 institutions in 1 country.

M A Berny-LangDepartment of Biomedical Engineering, School of Medicine, Oregon Health & Science University, 3303 SW Bond Ave, Portland, OR 97239, USA.
J E Aslan
G W Tormoen
I A Patel
P E Bock
A Gruber
O J T McCarty
Oregon Health & Science University · USVanderbilt University Medical Center · US

Funding

TopologyU54CA143906 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KUHN, PETER · 2009 to 2014
$10.2M
Characterization of Coagulation Factor-platelet Interactions: Role of FXIR01HL101972 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Owen J McCarty · 2010 to 2026
$8.5M
FACTOR VA INTERACTIONS REGULATING PROTHROMBIN ACTIVATIONR01HL038779 · NHLBI · VANDERBILT UNIVERSITY · PI BOCK, PAUL E · 1994 to 2010
$3.0M
Mechanism of Staphylocoagulase-activated Blood ClottingR37HL071544 · NHLBI · VANDERBILT UNIVERSITY · PI BOCK, PAUL E · 2004 to 2012
$2.9M
NCI NIH HHS 1U54CA143906-01NCI NIH HHS U54 CA143906NHLBI NIH HHS R01 HL038779NHLBI NIH HHS R01HL038779NHLBI NIH HHS R01 HL101972NHLBI NIH HHS R01HL101972NHLBI NIH HHS R37 HL071544NHLBI NIH HHS R37HL071544NHLBI NIH HHS T32 HL00778118
6 · The paper itself

Abstract

The routine observation of tumor emboli in the peripheral blood of patients with carcinomas raises questions about the clinical relevance of these circulating tumor cells. Thrombosis is a common clinical manifestation of cancer, and circulating tumor cells may play a pathogenetic role in this process. The presence of coagulation-associated molecules on cancer cells has been described, but the mechanisms by which circulating tumor cells augment or alter coagulation remains unclear. In this study we utilized suspensions of a metastatic adenocarcinoma cell line, MDA-MB-231, and a non-metastatic breast epithelial cell line, MCF-10A, as models of circulating tumor cells to determine the thrombogenic activity of these blood-foreign cells. In human plasma, both metastatic MDA-MB-231 cells and non-metastatic MCF-10A cells significantly enhanced clotting kinetics. The effect of MDA-MB-231 and MCF-10A cells on clotting times was cell number-dependent and inhibited by a neutralizing antibody to tissue factor (TF) as well as inhibitors of activated factor X and thrombin. Using fluorescence microscopy, we found that both MDA-MB-231 and MCF-10A cells supported the binding of fluorescently labeled thrombin. Furthermore, in a model of thrombus formation under pressure-driven flow, MDA-MB-231 and MCF-10A cells significantly decreased the time to occlusion. Our findings indicate that the presence of breast epithelial cells in blood can stimulate coagulation in a TF-dependent manner, suggesting that tumor cells that enter the circulation may promote the formation of occlusive thrombi under shear flow conditions.

Indexed as

AdenocarcinomaBlood CoagulationBreast NeoplasmsCell LineCell Line, TumorFemaleHumansThrombosis

Identifiers

PMID21301066
PMCPMC3209705
OpenAlexW2096500843

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.