INTRAHETEROSEQ
Financiado
Molecular characterization of the role of intra tumor heterogeneity in cancer pr...
Molecular characterization of the role of intra tumor heterogeneity in cancer progression and metastasis
Cancer is caused by somatically acquired changes in the DNA. Some of these changes fall in cancer genes, conferring clonal selective advantage to the cells that carry the mutant alleles. Identifying these genes/pathways is of vit...
Cancer is caused by somatically acquired changes in the DNA. Some of these changes fall in cancer genes, conferring clonal selective advantage to the cells that carry the mutant alleles. Identifying these genes/pathways is of vital importance for a correct understanding of cancer biology as well as for the diagnosis and treatment of human malignancies. In this respect, the use of genetically modified mice has been extremely useful in the past for characterizing the molecular pathways involved in cancer progression. The remarkable progress made during the last two decades on the genetic modification of mouse genomes offers unique opportunities to investigate different aspects of tumor molecular behavior, impossible to study on human samples.
Recently, the advent of next-generation sequencing technologies has provided new strategies for the systematic genome-wide identification of somatic changes in cancer cell genomes. Using these technologies, we and others have characterized the high intra-tumor heterogeneity observed in some human tumors. Although the exact significance of this heterogeneity is uncertain, it seems to be responsible for key aspects in the management of cancer patients such as metastasis predisposition and tissue specificity or treatment resistance.
Taking advantage of next-generation sequencing, we propose to finely characterize the intra-tumor heterogeneity evolution during the progression of tumors induced in a mouse model of pancreatic cancer, as well as, for the first time, to purify the different cell populations these primary tumors are composed of. A complete genomic and transcriptomic characterization of these populations followed by posterior functional assays will help us to identify the genes/pathways involved in tumor progression as well as metastatic potential and its tissue specificity. This new knowledge could finally contribute to a better understanding of cancer and to the design of more efficient anti-tumor therapies
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Duración del proyecto: 66 meses
Fecha Inicio: 2015-04-30
Fecha Fin: 2020-10-31
Fecha Fin: 2020-10-31
Línea de financiación: concedida
El organismo H2020 notifico la concesión del proyecto el día 2020-10-31
Línea de financiación objetivo
El proyecto se financió a través de la siguiente ayuda:
ERC-StG-2014:
ERC Starting Grant
Cerrada
hace 10 años
Presupuesto
El presupuesto total del proyecto asciende a
1M€
Líder del proyecto
UNIVERSIDAD DE CANTABRIA
No se ha especificado una descripción o un objeto social para esta compañía.
Total investigadores
469
Total investigadores
469