Evidence map›Paper›PMID 37517779›Full record

ReviewAdvanced drug delivery reviews2023

The role of coagulome in the tumor immune microenvironment.

Riajul Wahab, Md Mahedi Hasan, Zulfikar Azam, Paul J Grippo, Taslim A Al-Hilal

Open access · greenAbstract readReview
In one paragraph

Review in Advanced drug delivery reviews, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Role of comorbidities and medication on immunotherapy efficacy in cSCC: A DeCOG multicentre analysis.Journal of the European Academy of Dermatology and Venereology : JEADV · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Immunity and coagulation.Journal of translational medicine · 2026
    Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Observational
  12. Article
  13. Article
  14. Role of Clot Formation and Plasminogen Activation in Lower Urinary Tract Pathologies.Arteriosclerosis, thrombosis, and vascular biology · 2025
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
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

5 authors at 2 institutions in 1 country.

Riajul WahabDepartment of Pharmaceutical Sciences, School of Pharmacy, University of Texas at El Paso, El Paso, TX 79968, USA.
Md Mahedi HasanDepartment of Pharmaceutical Sciences, School of Pharmacy, University of Texas at El Paso, El Paso, TX 79968, USA; Department of Environmental Science & Engineering, College of Science, University of Texas at El Paso, El Paso, TX 79968, USA.
Zulfikar AzamDepartment of Pharmaceutical Sciences, School of Pharmacy, University of Texas at El Paso, El Paso, TX 79968, USA.
Paul J GrippoDepartment of Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Taslim A Al-HilalDepartment of Pharmaceutical Sciences, School of Pharmacy, University of Texas at El Paso, El Paso, TX 79968, USA; Department of Environmental Science & Engineering, College of Science, University of Texas at El Paso, El Paso, TX 79968, USA. Electronic address: taalhilal@utep.edu.
The University of Texas at El Paso · USUniversity of Illinois Chicago · US

Funding

Targeting of Doppel-axis to Control Lung Tumor Angiogenesis and ImmunityR01CA262788 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Taslim A Al-Hilal · 2022 to 2026
$1.4M
Priming pancreatic ductal adenocarcinoma using blood thinners to sensitize the efficacy of checkpoint immunotherapySC1GM144171 · NIGMS · UNIVERSITY OF TEXAS EL PASO · PI AL-HILAL, TASLIM A · 2022 to 2023
$740k
The role of tumor endothelium-specific prion-gene PRND in epithelial ovarian cancerR21CA264627 · NCI · UNIVERSITY OF UTAH · PI AL-HILAL, TASLIM A · 2022 to 2023
$387k
NCI NIH HHS R01 CA262788NCI NIH HHS R21 CA264627NIGMS NIH HHS SC1 GM144171
6 · The paper itself

Abstract

The rising incidence and persistent thrombosis in multiple cancers including those that are immunosuppressive highlight the need for understanding the tumor coagulome system and its role beyond hemostatic complications. Immunotherapy has shown significant benefits in solid organ tumors but has been disappointing in the treatment of hypercoagulable cancers, such as glioblastoma and pancreatic ductal adenocarcinomas. Thus, targeting thrombosis to prevent immunosuppression seems a clinically viable approach in cancer treatment. Hypercoagulable tumors often develop fibrin clots within the tumor microenvironment (TME) that dictates the biophysical characteristics of the tumor tissue. The application of systems biology and single-cell approaches highlight the potential role of coagulome or thrombocytosis in shaping the tumor immune microenvironment (TIME). In-depth knowledge of the tumor coagulome would provide unprecedented opportunities to better predict the hemostatic complications, explore how thrombotic stroma modulates tumor immunity, reexamine the significance of clinical biomarkers, and enable steering the stromal versus systemic immune response for boosting the effectiveness of immune checkpoint inhibitors in cancer treatment. We focus on the role of coagulation factors in priming a suppressive TIME and the huge potential of existing anticoagulant drugs in the clinical settings of cancer immunotherapy.

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsHumansImmunosuppression TherapyImmunotherapyTumor MicroenvironmentCancer immunotherapyDrug transport barrierImmunosuppressionTumor coagulomeTumor microenvironment

Identifiers

PMID37517779
PMCPMC11099942
OpenAlexW4385336067

What Socratic 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 Socratic graph.