EXCEED · Exosome Characterization Platform for Early Detection of Breast Cancer
Horizon Europe — Marie Skłodowska-Curie Actions
- Duration
- 2023-04-01 → 2026-03-31
- EU contribution
- €268,803
- Participants
- 2
- Scheme
- HORIZON-TMA-MSCA-PF-GF
Lines connect the coordinator with its partners.
Results in brief
Exosome Characterization Platform for Early Detection of Breast Cancer
Extracellular vesicles (EVs) are nanoscale particles naturally released by cells into biological fluids such as blood, urine, and saliva. Because EVs carry proteins, nucleic acids, lipids, and other molecular information originating from their parent cells, they have emerged as promising biomarkers for non-invasive disease detection and monitoring. However, existing technologies for EV analysis often require complex sample preparation, fluorescent labeling, expensive instrumentation, or extensive laboratory infrastructure, limiting their broader adoption in research and clinical settings. The EXCEED project (“Exosome Characterization Platform for Early Detection of Breast Cancer”) aimed to develop innovative label-free technologies for the detection, sizing, and characterization of EVs and other nanoscale biological particles. The project was supported through the Marie Skłodowska-Curie Actions (MSCA) Global Fellowship programme and conducted through collaboration between Stanford University (United States) and Koç University (Türkiye). The fellowship combined expertise in optical engineering, interferometric microscopy, Raman spectroscopy, artificial intelligence, computational imaging, and translational medicine to create new tools for liquid biopsy applications. The central objective of the project was to develop a multimodal platform capable of characterizing individual EVs without the need for fluorescent labels or amplification methods. To achieve this goal, the project integrated interferometric microscopy for highly sensitive particle detection and sizing with Raman spectroscopy for molecular characterization. Advanced computational approaches, including Bayesian inference and machine learning, were also developed to improve data analysis and enable quantitative characterization of nanoscale particles. Together, these technologies provide complementary physical and molecular information from individual EVs, creating new opportunities for liquid biopsy and biomarker discovery. Although initially focused on breast cancer, the technologies developed during the project proved broadly applicable and were successfully extended to additional biomedical applications of other extracellular vesicle-based translational studies. The project also established new international collaborations and follow-on research activities involving larger clinical cohorts and future diagnostic applications. By advancing label-free characterization of extracellular vesicles and nanoscale biomarkers, EXCEED contributes to ongoing efforts in personalized medicine, early disease detection, and non-invasive diagnostics. The project supports European priorities in health innovation, digital technologies, and translational research, while creating opportunities for future scientific, clinical, and commercial impact. In the long term, the technologies developed through EXCEED may contribute to more accessible, affordable, and information-rich diagnostic tools for a wide range of diseases.
Data: CORDIS, © European Union
Project objective
Breast cancer is the most common cancer among women worldwide. Early detection is the most critical element, as the survival rate increases by up to 99%. Although there are conventional screening techniques such as mammography, breast cancer is still the second leading cause of cancer death in women. One of the holy grails in cancer research is to develop a blood test for early detection. Sensitive, non-invasive, and easy-to-use liquid biopsy techniques will revolutionize cancer diagnosis and treatment monitoring. The goal of this project is to develop a complete platform for the isolation and label-free optical characterization of biological nanoparticles called exosomes extracted from blood. Exosomes are secreted from the cells into the body fluids and play an important role in intercellular communication. These particles are emerged as potential biomarkers for liquid biopsy applications, as they carry information about their original cell. However, the translation of exosome-based analyses from research labs to clinical settings is limited due to the lack of efficient isolation and quantification tools available. We aim to develop a novel exosome characterization platform, named multimodal Interferometric-Raman imaging platform to detect and quantify exosomes at a single-particle level without using any labels. The combination of the label-free imaging capability of interferometric microscopy and the chemical content information provided by Raman spectroscopy will be an important step for exosome-based diagnostics applications. The proposed system will be integrated into a state-of-the-art isolation tool, creating complete isolation and multiparameter characterization platform. The proposed platform will be tested with the exosomes isolated from tumor cells to determine possible biomarkers that can be used for diagnosis. The diagnostic capability of the system will be validated with healthy donors and breast cancer patients(30 persons each)
Original text from CORDIS.
Participants
- KOC UNIVERSITY · IstanbulCoordinatorTürkiye
- BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY · STANFORDUnited States
Links
- View on CORDIS
- DOI: 10.3030/101066038
- https://ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e504cdef3c&appId=PPGMS
- https://ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e52e4bb14e&appId=PPGMS
Data: CORDIS, © European Union
