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Organ-on-chip technologies at the cancer-thrombosis interface
Inês Soares Marques1, Raquel Almeida2, Pedro F Costa3
1BIOFABICS - 3D Biotissue Analogues, Porto, Portugal; Institute for Research and Innovation in Health (i3S), University of Porto, Porto, Portugal; School of Medicine and Biomedical Sciences (ICBAS), University of Porto, Porto, Portugal.
Trends in Biotechnology
|October 26, 2025
Summary
Cancer-associated thrombosis (CAT) is a major cause of death in cancer patients. Organ-on-chip technology offers a new way to study complex tumor-haemostasis interactions and develop better treatments.
Area of Science:
- Biomedical Engineering
- Oncology
- Hematology
Background:
- Cancer-associated thrombosis (CAT) is a significant cause of mortality in cancer patients.
- Tumour-haemostasis interactions are the primary drivers of CAT.
- Traditional research models struggle to fully replicate the complexity of CAT.
Purpose of the Study:
- To explore the potential of organ-on-chip (OoC) technology in studying cancer-associated thrombosis.
- To enhance the understanding of the mechanisms underlying CAT.
- To identify new therapeutic strategies for managing CAT.
Main Methods:
- Utilizing organ-on-chip models to simulate tumour-haemostasis interactions.
- Investigating the biological processes involved in CAT within the OoC environment.
- Analyzing the efficacy of potential therapeutic interventions using OoC platforms.
Main Results:
- OoC models provide a more complex and accurate representation of tumour-haemostasis interactions compared to traditional methods.
- The study elucidated key mechanisms driving cancer-associated thrombosis.
- Preliminary data suggests potential for OoC in evaluating novel CAT therapies.
Conclusions:
- Organ-on-chip technology presents a promising platform for advancing the study of cancer-associated thrombosis.
- OoC offers enhanced insights into CAT mechanisms, paving the way for improved therapeutic strategies.
- This approach holds potential for personalized medicine in oncology and hematology.
Keywords:
cancer-associated thrombosismicrofluidicmicrophysiological systemorgan-on-chippreclinical model
