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| Funder | European Commission |
|---|---|
| Recipient Organization | Ludwig-Maximilians-Universitaet Muenchen |
| Country | Germany |
| Start Date | Jan 01, 2024 |
| End Date | Dec 31, 2028 |
| Duration | 1,826 days |
| Number of Grantees | 1 |
| Roles | Coordinator |
| Data Source | European Commission |
| Grant ID | 101115861 |
Early cancer detection could increase curative treatment and long-term survival.
Dying cells release small DNA fragments wrapped around a core of histone proteins into the bloodstream, so-called circulating cell-free nucleosomes (cf-nucleosomes).
They carry DNA sequence information and histone modifications stable in blood, reflecting promising epigenomic disease biomarkers.
But, the low proportion of cf-nucleosomes originating from cancerous cells versus the large background of nucleosomes arising from dying blood cells poses significant challenges for early cancer detection using circulating cf-nucleosomes.
In EpiCblood, I will tackle these challenges and propose two complementary strategies to increase the number of cancer-signature cf-nucleosomes for cancer detection and tumor classification.
In the first strategy, I will employ my previously developed synthetic histone modification readers to profile abundant histone modifications on cf-nucleosomes allowing me to seize up to 35 percent of the human genome non-invasively.
I will prove this technologys concept by detecting earlier stages of pancreatic cancer and simultaneously classifying molecular tumor subtypes.
Furthermore, I hypothesize that tumorigenesis gives rise to cancer-specific genomic sites decorated with combinatorial histone marks, so-called bivalent regions, found explicitly in cancer and not in healthy adult cell types.
In the second strategy, I will employ a computational pipeline to map cancer-specific bivalent sites across multiple cancer genomes.
I will use my well-established combinatorial histone mark readers to test their diagnostic potential as cancer-specific biomarkers in blood plasma from healthy donors and cancer patients. My genomics expertise and proven technology provide an excellent basis for accomplishing the planned goals.
EpiCblood will be a major step towards developing precise and rich liquid biopsy assays for multiple clinical applications in cancer management.
Ludwig-Maximilians-Universitaet Muenchen
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