Evidence map›Paper›PMID 33057845›Full record

ArticleCancer immunology, immunotherapy : CII2021

A pan-cancer analysis of the human tumor coagulome and its link to the tumor immune microenvironment.

Zuzana Saidak, Simon Soudet, Marine Lottin, Valéry Salle, Marie-Antoinette Sevestre, Florian Clatot, Antoine Galmiche

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
5.0field-weighted citation impact, top 3% 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

69 citing papers in PubMed, 112 citations in OpenAlex.

  1. First-in-Humans PET Imaging of Tissue Factor in Patients with Primary and Metastatic Cancers UsingJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2022
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  16. The Dynamic Landscape of the Coagulome of Metastatic Malignant Melanoma.International journal of molecular sciences · 2025
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9 more citing papers are in PubMed but not listed here.

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 3 institutions in 1 country.

Zuzana SaidakEA7516 CHIMERE, Université de Picardie Jules Verne, Amiens, France. Saidak.Zuzana@chu-amiens.fr.
Simon SoudetService de Médecine Vasculaire, CHU, Amiens, France.
Marine LottinService de Biochimie, Centre de Biologie Humaine (CBH), CHU Amiens Sud, Avenue Laennec, 80054, Amiens Cedex, France.
Valéry SalleService de Biochimie, Centre de Biologie Humaine (CBH), CHU Amiens Sud, Avenue Laennec, 80054, Amiens Cedex, France.
Marie-Antoinette SevestreEA7516 CHIMERE, Université de Picardie Jules Verne, Amiens, France.
Florian ClatotCentre Henri Becquerel, Rouen, France.
Antoine GalmicheEA7516 CHIMERE, Université de Picardie Jules Verne, Amiens, France. Galmiche.antoine@chu-amiens.fr.ORCID http://orcid.org/0000-0002-5836-4646
Centre Hospitalier Universitaire Amiens-Picardie · FRSociété Française de Médecine Vasculaire · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveSolid tumors often establish a procoagulable state that can lead to venous thromboembolism (VTE). Although some of the key genes involved in this process are known, no previous study has compared the "coagulome", i.e., the expression of coagulation/fibrinolysis genes, across different primary tumor types. It is also unclear whether the coagulome is associated with specific characteristics of the tumor microenvironment (TME). We aimed to address this question.

methodsWe analyzed the expression of the genes F3, PLAU, PLAT, PLAUR, SERPINB2, and SERPINE1 in 32 cancer types using data from The Cancer Genome Atlas (TCGA) and other freely available resources.

resultsWe identified specific expression patterns of procoagulant and fibrinolytic genes. The expression of the Tissue Factor (F3) was found to be tumor type dependent, with the highest expression in glioblastoma (GBM), a highly procoagulable tumor type. Conversely, high expression of the fibrinolysis gene cluster PLAU, PLAUR, SERPINE1 was consistently linked to the characteristics of the TME (monocytic infiltration) and high expression of important checkpoints of the immune response, such as PD-L2 and CD276/B7-H3.

conclusionThese tumor-specific patterns of expression might partially explain the differences in VTE risk among tumor types. We propose that biomarkers of coagulation fibrinolysis might provide valuable information about the TME in cancer patients.

Indexed as

Gene Expression Regulation, NeoplasticTranscriptomeBiomarkers, TumorBlood CoagulationGene Expression ProfilingHumansNeoplasmsNeovascularization, PathologicTumor MicroenvironmentBiomarkers, TumorCancer-associated thrombosisCoagulomeFibrinolysisThe Cancer Genome Atlas (TCGA)Tissue factorTumor microenvironment

Identifiers

PMID33057845
PMCPMC10991611
OpenAlexW3092782633

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.