Evidence map›Paper›PMID 30760580›Full record

ArticleScience translational medicine2019

Platelet decoys inhibit thrombosis and prevent metastatic tumor formation in preclinical models.

Anne-Laure Papa, Amanda Jiang, Netanel Korin, Michelle B Chen, Erin T Langan, Anna Waterhouse, Emma Nash, Jildaz Caroff, Amanda Graveline, Andyna Vernet and 6 more

Abstract read
PubMed Publisher
In one paragraph

Article in Science translational medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

41 citing papers in PubMed, 81 citations in OpenAlex.

  1. Niches in cancer: from primary tumors to metastatic disease.Journal of hematology & oncology · 2026
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  5. Engineering platelets as cancer therapeutics.Nature reviews. Clinical oncology · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 3 institutions in 1 country.

Anne-Laure PapaWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA. don.ingber@wyss.harvard.edu alpapa@gwu.edu.ORCID 0000-0001-8282-5564
Amanda JiangVascular Biology Program and Department of Surgery, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.ORCID 0000-0001-7545-2667
Netanel KorinWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA.ORCID 0000-0001-7244-889X
Michelle B ChenDepartment of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Erin T LanganNew England Center for Stroke Research, Department of Radiology, University of Massachusetts, Worcester, MA 01655, USA.ORCID 0000-0002-8271-1177
Anna WaterhouseWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA.ORCID 0000-0003-1498-9393
Emma NashWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA.ORCID 0000-0001-6798-0590
Jildaz CaroffNew England Center for Stroke Research, Department of Radiology, University of Massachusetts, Worcester, MA 01655, USA.ORCID 0000-0002-0029-1835
Amanda GravelineWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA.ORCID 0000-0002-2626-4093
Andyna VernetWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA.
Akiko MammotoVascular Biology Program and Department of Surgery, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Tadanori MammotoVascular Biology Program and Department of Surgery, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Abhishek JainWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA.ORCID 0000-0003-2235-5139
Roger D KammDepartment of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.ORCID 0000-0002-7232-304X
Matthew J GounisNew England Center for Stroke Research, Department of Radiology, University of Massachusetts, Worcester, MA 01655, USA.ORCID 0000-0002-8034-2785
Donald E IngberWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA. don.ingber@wyss.harvard.edu alpapa@gwu.edu.ORCID 0000-0002-4319-6520
Harvard University · USBoston Children's Hospital · USMassachusetts Institute of Technology · US

Funding

Research Supplement - Quantitative analyses of tumor cell extravasationU01CA202177 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI KAMM, ROGER D · 2015 to 2020
$4.2M
NCI NIH HHS U01 CA202177
6 · The paper itself

Abstract

Platelets are crucial for normal hemostasis; however, their hyperactivation also contributes to many potentially lethal pathologies including myocardial infarction, stroke, and cancer. We hypothesized that modified platelets lacking their aggregation and activation capacity could act as reversible inhibitors of platelet activation cascades. Here, we describe the development of detergent-extracted human modified platelets (platelet decoys) that retained platelet binding functions but were incapable of functional activation and aggregation. Platelet decoys inhibited aggregation and adhesion of platelets on thrombogenic surfaces in vitro, which could be immediately reversed by the addition of normal platelets; in vivo in a rabbit model, pretreatment with platelet decoys inhibited arterial injury-induced thromboembolism. Decoys also interfered with platelet-mediated human breast cancer cell aggregation, and their presence decreased cancer cell arrest and extravasation in a microfluidic human microvasculature on a chip. In a mouse model of metastasis, simultaneous injection of the platelet decoys with tumor cells inhibited metastatic tumor growth. Thus, our results suggest that platelet decoys might represent an effective strategy for obtaining antithrombotic and antimetastatic effects.

Indexed as

AnimalsBlood PlateletsCell Line, TumorDisease Models, AnimalExtracellular MatrixFemaleHumansMice, Inbred BALB CMice, NudeNeoplasm MetastasisPlatelet AdhesivenessPlatelet AggregationRabbitsReceptors, Cell SurfaceThrombosisReceptors, Cell Surface

Identifiers

PMID30760580
OpenAlexW2913935991

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.