Evidence map›Paper›PMID 39190500›Full record

ArticleJCI insight2024

Deconvolution of the tumor-educated platelet transcriptome reveals activated platelet and inflammatory cell transcript signatures.

Jerome M Karp, Aram S Modrek, Ravesanker Ezhilarasan, Ze-Yan Zhang, Yingwen Ding, Melanie Graciani, Ali Sahimi, Michele Silvestro, Ting Chen, Shuai Li and 4 more

Abstract read
In one paragraph

Article in JCI insight, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Platelets as regulators of cancer immunity: mechanisms and therapeutic perspectives.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

14 authors.

Jerome M KarpDepartment of Radiation Oncology, NYU Grossman School of Medicine, New York, New York, USA.
Aram S ModrekDepartment of Radiation Oncology, Keck School of Medicine of University of Southern California, Los Angeles, California, USA.
Ravesanker EzhilarasanDepartment of Radiation Oncology, NYU Grossman School of Medicine, New York, New York, USA.
Ze-Yan ZhangDepartment of Radiation Oncology, NYU Grossman School of Medicine, New York, New York, USA.
Yingwen DingDepartment of Radiation Oncology, NYU Grossman School of Medicine, New York, New York, USA.
Melanie GracianiDepartment of Radiation Oncology, NYU Grossman School of Medicine, New York, New York, USA.
Ali SahimiDepartment of Radiation Oncology, NYU Grossman School of Medicine, New York, New York, USA.
Michele SilvestroDepartment of Cell Biology and.
Ting ChenLaura and Isaac Perlmutter Cancer Center, NYU Grossman School of Medicine, New York, New York, USA.
Shuai LiLaura and Isaac Perlmutter Cancer Center, NYU Grossman School of Medicine, New York, New York, USA.
Kwok-Kin WongLaura and Isaac Perlmutter Cancer Center, NYU Grossman School of Medicine, New York, New York, USA.
Bhama RamkhelawonDepartment of Cell Biology and.
Krishna Pl BhatDepartment of Cancer Biology, Mayo Clinic, Scottsdale, Arizona, USA.
Erik P SulmanDepartment of Radiation Oncology, NYU Grossman School of Medicine, New York, New York, USA.

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ANIRBAN MAITRA · 1985 to 2026
$83.1M
Bidirectional interaction of platelets and tumor cells in patients with glioblastomaR01CA225963 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BHAT, KRISHNA PL, SULMAN, ERIK · 2019 to 2023
$2.7M
NCI NIH HHS P30 CA016087NCI NIH HHS R01 CA225963
6 · The paper itself

Abstract

Tumor-educated platelets (TEPs) are a potential method of liquid biopsy for the diagnosis and monitoring of cancer. However, the mechanism underlying tumor education of platelets is not known, and transcripts associated with TEPs are often not tumor-associated transcripts. We demonstrated that direct tumor transfer of transcripts to circulating platelets is an unlikely source of the TEP signal. We used CDSeq, a latent Dirichlet allocation algorithm, to deconvolute the TEP signal in blood samples from patients with glioblastoma. We demonstrated that a substantial proportion of transcripts in the platelet transcriptome are derived from nonplatelet cells, and the use of this algorithm allows the removal of contaminant transcripts. Furthermore, we used the results of this algorithm to demonstrate that TEPs represent a subset of more activated platelets, which also contain transcripts normally associated with nonplatelet inflammatory cells, suggesting that these inflammatory cells, possibly in the tumor microenvironment, transfer transcripts to platelets that are then found in circulation. Our analysis suggests a useful and efficient method of processing TEP transcriptomic data to enable the isolation of a unique TEP signal associated with specific tumors.

Indexed as

Blood PlateletsGlioblastomaTranscriptomeTumor MicroenvironmentAlgorithmsBrain NeoplasmsGene Expression ProfilingHumansInflammationPlatelet ActivationBrain cancerOncologyPlatelets

Identifiers

PMID39190500
PMCPMC11466191

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Registered trials

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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.