Evidence map›Paper›PMID 26219246›Full record

ReviewBlood reviews2016

The prothrombotic activity of cancer cells in the circulation.

Annachiara Mitrugno, Garth W Tormoen, Peter Kuhn, Owen J T McCarty

Abstract readReview
In one paragraph

Review in Blood reviews, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
–field-weighted citation impact
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

51 citing papers in PubMed.

  1. Article
  2. Thrombin generation profiling in multiple myeloma: a comprehensive evaluation of prothrombotic state.Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis · 2026
    Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. What to Do When There Is Something Unexpected?Life (Basel, Switzerland) · 2024
    Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. The Applications and Challenges of the Development ofCellular and molecular bioengineering · 2023
    Review
  18. Review
  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

4 authors.

Annachiara MitrugnoDepartment of Biomedical Engineering, School of Medicine, Oregon Health & Science University, Portland, OR, USA; Department of Cell, Developmental and Cancer Biology, School of Medicine, Oregon Health & Science University, Portland, OR, USA; Divison of Hematology & Medical Oncology, School of Medicine, Oregon Health & Science University, Portland, OR, USA. Electronic address: mitrugno@ohsu.edu.
Garth W TormoenDepartment of Biomedical Engineering, School of Medicine, Oregon Health & Science University, Portland, OR, USA. Electronic address: tormoeng@ohsu.edu.
Peter KuhnDepartment of Biological Sciences, University of Southern California, Los Angeles, CA, USA. Electronic address: pkuhn@usc.edu.
Owen J T McCartyDepartment of Biomedical Engineering, School of Medicine, Oregon Health & Science University, Portland, OR, USA; Department of Cell, Developmental and Cancer Biology, School of Medicine, Oregon Health & Science University, Portland, OR, USA; Divison of Hematology & Medical Oncology, School of Medicine, Oregon Health & Science University, Portland, OR, USA. Electronic address: mccartyo@ohsu.edu.

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
Training in the Molecular Basis of Skin/Mucosa PathobiologyT32CA106195 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI KULESZ-MARTIN, MOLLY F. · 2004 to 2018
$3.8M
FXI and SepsisR01GM116184 · NIGMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI LUPU, FLOREA, MCCARTY, OWEN J · 2015 to 2018
$1.9M
NCI NIH HHS T32 CA106195NCI NIH HHS U54 CA143906NHLBI NIH HHS R01 HL101972NIGMS NIH HHS R01 GM116184
6 · The paper itself

Abstract

The hemostatic system is often subverted in patients with cancer, resulting in life-threatening venous thrombotic events. Despite the multifactorial and complex etiology of cancer-associated thrombosis, changes in the expression and activity of cancer-derived tissue factor (TF) - the principle initiator of the coagulation cascade - are considered key to malignant hypercoagulopathy and to the pathophysiology of thrombosis. However, many of the molecular and cellular mechanisms coupling the hemostatic degeneration to malignancy remain largely uncharacterized. In this review we discuss some of the tumor-intrinsic and tumor-extrinsic mechanisms that may contribute to the prothrombotic state of cancer, and we bring into focus the potential for circulating tumor cells (CTCs) in advancing our understanding of the field. We also summarize the current status of anti-coagulant therapy for the treatment of thrombosis in patients with cancer.

Indexed as

Gene Expression Regulation, NeoplasticAnticoagulantsAntineoplastic AgentsBlood CoagulationBlood PlateletsFactor VIIaFibrinFibrinogenHumansNeoplasmsNeoplastic Cells, CirculatingPlatelet ActivationProthrombinThromboplastinThrombosisAnticoagulantsAntineoplastic AgentsFactor IIaFactor VIIaFibrinFibrinogenProthrombinThromboplastinCancerCirculating tumor cellsCoagulationPlateletsThrombosisTissue factor

Identifiers

PMID26219246
PMCPMC4942124

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.