ORION · HydrOdynamics & biomechanics of canceR cell mIgration in heterOgeNeous media
„Хоризонт Европа“ — Действия „Мария Склодовска-Кюри“
- Период
- 2023-04-01 → 2025-03-31
- Финансиране от ЕС
- 187 624 €
- Участници
- 2
- Схема
- HORIZON-TMA-MSCA-PF-EF
Линиите свързват координатора с партньорите.
Накратко на български
Физическите сили и движението на раковите клетки през тъкани и кръвоносни съдове се анализират чрез микрофлуидни опити и компютърни модели. Разбирането на тези процеси помага за разработването на нови стратегии за ранно откриване на метастазите.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
HydrOdynamics & biomechanics of canceR cell mIgration in heterOgeNeous media
Metastasis—the spread of cancer from a primary tumor to distant organs—remains one of the most complex and least understood aspects of cancer progression, responsible for over 90% of cancer-related deaths. A key step in this process is the migration of circulating tumor cells (CTCs) through the heterogeneous and mechanically complex environments of the extracellular matrix (ECM) and microvasculature. Despite its clinical significance, the physical and mechanical factors governing CTC transport, deformation, and retention in these environments remain largely unexplored. Traditional cancer research has focused predominantly on genetic and biochemical signaling pathways, leaving a gap in our understanding of the physical forces and fluid dynamic conditions that influence metastasis. The ORION project was designed to fill this critical knowledge gap by investigating how hydrodynamic forces, microstructural heterogeneity, and mechanobiological properties of tumor cells interact to govern their migration behavior. The overarching objective was to develop a fundamental understanding of CTC transport through confined porous environments, using a combination of microfluidic experimentation, computational fluid dynamics (CFD), rheological modeling, and mechanobiology. By integrating these approaches, ORION aimed to reveal the physical principles underlying key metastatic behaviors such as cell trapping, deformation, collective motility, and the response to chemotactic gradients like TGF-β. The expected impact of ORION extends across multiple domains. Scientifically, the project contributes a novel and quantifiable framework for studying cancer cell transport in complex microenvironments. Biomedically, the insights gained can help building new strategies for early detection of metastatic potential, improve therapeutic targeting, and inspire bioengineered platforms for drug testing or cell sorting. Industrially, the findings offer pathways toward the development of microfluidic systems for diagnostic or therapeutic use. Societally, understanding and ultimately disrupting the physical mechanisms of metastasis could lead to measurable improvements in patient survival and reduce the burden on healthcare systems. Situated within the broader strategic landscape of Horizon Europe and the EU’s Mission on Cancer, ORION supports the goal of reducing the societal impact of cancer by contributing to upstream prevention and more effective treatment strategies. Its interdisciplinary and translational nature aligns with Europe's commitment to cross-sectoral, high-impact biomedical innovation. While social sciences and humanities were not explicitly integrated into this project, ORION’s focus on public health relevance and its potential to influence clinical practice make it highly aligned with societal priorities in healthcare.
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
So far medicine has not solved the workings of a formidable and scientifically challenging aspect of cancer: metastasis, the migration of circulating tumor cells (CTC) through the body. In this highly interdisciplinary project, expertise and techniques from fluid dynamics are employed to study how CTC move through the vascular network and what prompts them to do so. The complex interplay among hydrodynamics, biophysics of intracellular interactions, and biochemical signaling within vascular networks is unknown. Our understanding of these underlying processes is hindered by the complex heterogeneity in the vascular network, comprising of capillaries, veins and arteries with a wide range of size and structural diversity. To unravel these processes I bring my expertise in fluid dynamics and porous media together with the state-of-the-art facilities on experimental cancer mechanobiology and multiscale modeling at the host and secondment institutes. I will conduct microfluidic experiments and simulations by simplifying the vascular network as strategically designed pore-network models. First, I will study the two-way interactions between the heterogeneous flow field and the deformable CTCs that control their overall transport, deformation and trapping. A heterogeneous flow field also induces a spatially nonuniform scalar concentration across the medium. CTCs are highly sensitive to certain biochemicals that can alter motility and invasiveness of CTCs. I will investigate how the local gradients of such biochemicals in a heterogeneous microsystem influence CTC migration. Finally, I will study the collective migration of CTC clusters through the system and quantify the dynamic intracellular interaction by measuring membrane tension and intracellular adhesion forces. These investigations will provide novel understandings on cancer metastasis that I will strategically communicate to research communities, stakeholders and general public.
Оригинален текст от CORDIS (на английски).
Участници
- TECHNISCHE UNIVERSITEIT DELFT · DelftКоординаторНидерландия
- KOBENHAVNS UNIVERSITET · KOBENHAVNДания
Връзки
- Виж в CORDIS
- DOI: 10.3030/101111247
- https://ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e5059048f7&appId=PPGMS
- https://ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e51d691c40&appId=PPGMS
Данни: CORDIS, © Европейски съюз
