The results obtained from this research will allow to specify the risk of developing some type of cancer in the approximately 1,000 study participants, from those 300 high-risk families. Consequently, preventive medicine measures can be taken in these people, such as facilitating access to early detection programs, closer follow-up or even considering preventive surgeries when necessary. This will benefit not only the participants studied but also their relatives and other families who carry the same variants. In addition, in the long term, this greater knowledge about the relationship between each genetic variant and cancer will bring personalized medicine closer to the entire population, allowing for better diagnoses and individualized clinical management.<\/p>\n
Dr. Mercedes Robledo, head of the CNIO Hereditary Endocrine Cancer Group<\/a> and project participant, affirms that “IMPaCT_VUSCan will make it possible to identify in the coming years which genetic variants, among the thousands carried by an individual, are related to development of cancer, and that will allow us to anticipate the development of the disease and act accordingly.”<\/p>\n Currently, information is already available on some of these variants, thanks to which the Spanish National Health System has the capacity to detect and monitor those who carry them. “Family cancer units have already managed to halve the incidence of cancer in patients who are followed in these programs, and their life expectancy has increased up to ten years,” says Dr. Conxi L\u00e1zaro, principal investigator of the project and head of the Hereditary Cancer Group<\/a> of IDIBELL and coordinator of the Molecular Diagnostic Unit of the Catalan Institute of Oncology. And she continues: “But many variants that influence the risk of developing cancer remain to be identified.”<\/p>\n <\/p>\n Many genetic variants, but only some are relevant<\/strong><\/p>\n We are all carriers of thousands of genetic variants, most of which have no clinical relevance. One of the keys to this project is to identify, among all these variants, which ones are responsible for a predisposition to cancer. To do this, bioinformatics and artificial intelligence algorithms will be used to identify those that are most likely to have a significant physiological impact. \u201cWe will carry out tests with cell, animal and organoid models, among other tests, of those variants previously identified as potential culprits,” says Dr. L\u00e1zaro.<\/p>\n As variants of clinical interest are found, they will be included in the databases of the National Health System so that the entire population can benefit. On the other hand, the project will allow the creation of a map of resources, a network of contacts and a circuit in order to be able to analyze any variant of unknown function in the future. According to Dr. Robledo: “In order to carry out such an ambitious project, the collaboration of many groups, experts in different disciplines, in a consortium like the one we have formed is essential.”<\/p>\n In addition to CNIO and IDIBELL, IMPaCT_VUSCan has the participation of seven research centers throughout Spain, such as the Instituto de Investigaci\u00f3n Sanitaria Sant Pau (IIB Sant Pau<\/a>), el Instituto de Investigaci\u00f3n Sanitaria de Navarra (IdiSNA<\/a>), el Instituto de Investigaci\u00f3n Sanitaria Hospital Cl\u00ednico San Carlos (IdISSC<\/a>), la Fundaci\u00f3n P\u00fablica Galega de Medicina Xen\u00f3mica (FPGMX<\/a>), la Fundaci\u00f3n para el Fomento de la Investigaci\u00f3n Sanitaria y Biom\u00e9dica de la Comunitat Valenciana (Fisabio<\/a>), la Fundaci\u00f3n Instituto Investigaci\u00f3n Sanitaria Islas Baleares (IDISBA<\/a>) y el Instituto de Investigaci\u00f3n Sanitaria La Paz (IdiPaz<\/a>).<\/p>\n <\/p>\n Credit: Underbau\/CNIO<\/p>\n <\/p>\n The Bellvitge Biomedical Research Institute (IDIBELL) is a biomedical research center created in 2004. It is participated by the Bellvitge University Hospital and the Viladecans Hospital of the Catalan Institute of Health, the Catalan Institute of Oncology, the University of Barcelona and the City Council of L\u2019Hospitalet de Llobregat.<\/em><\/p>\n IDIBELL is a member of the Campus of International Excellence of the University of Barcelona HUBc and is part of the CERCA institution of the Generalitat de Catalunya. In 2009 it became one of the first five Spanish research centers accredited as a health research institute by the Carlos III Health Institute. In addition, it is part of the \u201cHR Excellence in Research\u201d program of the European Union and is a member of EATRIS and REGIC. Since 2018, IDIBELL has been an Accredited Center of the AECC Scientific Foundation (FCAECC).<\/em><\/p>\n","protected":false},"excerpt":{"rendered":" The project, promoted by IDIBELL and CNIO, together with seven other research institutes, will combine artificial intelligence with cutting-edge molecular biology techniques to provide predictive medicine tools to the National Health 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<\/p>\n