Author: pancanwp

The PanCanRisk results has been published on CORDIS and are available here:

PanCanRisk – Personalized bioinformatics for global cancer susceptibility identification and clinical management

Project ID: 635290
Start date: 2015-07-01, End date: 2018-06-30
Cancer sequencing studies have extensively investigated the landscape of somatic mutations that drive tumor development, however the importance of germline variation for cancer susceptibility has been neglected. We hypothesize that for cancer types affecting a large proportion…
Programme: H2020-EU.3.1.6., Country: ES

The Biomedical Research Institute A Coruña (INIBIC) organizes the V Edition of Biomedical Cancer Research Conference in Galicia (IBCG-2018). On October 4th, Ceres Fernández, will be sharig an oral communication on PanCanRisk’s results.

This conference will bring together basic and clinical experts who are working on the most innovative current research topics in human malignancies and animal models, including inmunooncolgy, metastasis-associated microbiota, tumor heterogeneity, cancer and inflammation and novel therapies. The purpose of this conference is to provide a stimulating and interactive environment, including a session to promote the participation of researchers at early stages of their training.

  • A joint investigation from 6 top research centers in Europe to improve the detection and prevention of cancer.
  • The PanCanRisk Consortium, led by Prof. Ángel Carracedo at the Galician Public Foundation for Genomic Medicine presented this week in Santiago de Compostela the advances and conclusion of the three-year work.

On 18-19 June 2018, Santiago de Compostela was the host of an international meeting on cancer genetics research: 13 scientists from top institutes in Spain, France and the UK participated on 18 and 19 June in the final meeting of the PanCanRisk project.

Led from Spain by the team of Prof. ÁngelCarracedo at the Galician Public Foundation for Genomic Medicine (FPGMX), PanCanRisk – Personalised Bioinformatic  For Global Cancer Susceptibility Identification & Clinical Management– was born to identify novel hereditary risk factors that predispose to cancer and to develop novel biomarkers of early diagnosis.

With almost 3M€ of European funding and over 20 researchers from the FPGMX, the Dexeus clinic and the CRG (Barcelona), the Institute Curie (Paris), the EBI and Protein Logic (Cambridge), the project proposed back in 2015 to improve the bioinformatic tools available in order to detect novel and rare variants that confer risk to developing cancer amongst the heaps of currently available genomic data.

The meeting highlighted the advances and results obtained during these three years. Over this time, the different teams have progressed in the development and optimization of novel discovery algorithms, the validation of results in clinical cohorts from screening programs and the functional verification of the data.

The most relevant result to date is the identification of two novel genes that increase the likelihood of developing breast and bowel cancers. These results show great promise for the identification of perhaps novel mechanisms in cancer development that may lead the way to the generation of novel and earlier diagnostic and predictive biomarkers.

Hence, the team will continue working on the functional implications and roles that these genes play in cancer. A better comprehension of these mechanisms could potentially aid in the development of novel and more targeted therapies that can help improve the life of cancer patients.

  • The European project PanCanRisk, with participation from the EBI-EMBL and Protein Logic, investigates new mechanisms of hereditary transmission of cancer in order to improve prevention and diagnosis
  • The European consortium, led by Ángel Carracedo’s team at the Galician Public Foundation of Genomic Medicine, will meet this week in Santiago de Compostela to evaluate the project’s achievements

In 2014, an ambitious European genetic research project started with the main objective of identifying new hereditary cancer risk factors. Led from Santiago de Compostela by the team of Dr. Ángel Carracedo at the Galician Public Foundation of Genomic Medicine, PanCanRisk –Personalised Bioinformatics For Global Cancer Susceptibility Identification & Clinical Management– involves over 20 researchers from six institutes and reference research centers across Europe, two of which are based here in Cambridge.

The project is based on the fact that current technologies allow us to obtain and analyze large amounts of genetic data quickly and relatively easily. Noting the need for an adapted statistical analysis, they propose to improve the current algorithms by developing new methods. The goal: to find new genes related to the risk of developing cancer among the tide of currently available data.

The solidity of the approach and the excellence of the research teams involved warranted funding for 2.9M € from the European Union H2020 program for a three-year project.

In addition to the large-scale statistical analysis, the project also considers the validation of the results in real samples of patients obtained from usual clinical processes, such as colon and breast screening programs. Subsequently, functional models that can be applied to clinical practice will be designed, aimed to improve detection, prevention and diagnostic protocols.

Today, the PanCanRisk team faces the final stretch of the project. On June 18th an 19th, an international meeting will be held in Santiago de Compostela to share the progress and results obtained. We will know then if PanCanRisk can deliver on their promise to deliver an earlier diagnosis and more tailored risk screening strategies.

Where: Santiago de Compostela (España)     When: 18/09/2017 – 20/09/2017

A new brochure for recruitment of patients launched

The PanCanRisk project is a laboratory test designed to study genetic material. It consists of analyzing regions of the human genome (PanCanRisk test) to detect genetic alterations that may be related to a genetic predisposition to cancer. Its objective is to define the genes and genetic variants associated with the risk of breast cancer, and to compare the frequency and type of genomic variants between the populations of breast cancer cases and those that serve as control (with no known background).

Clínica de la Mujer Dexeus (one of the partners of the PanCanRisk project in Spain) has launched a leaflet in order to inform women about the possibility of taking part in research studies in the framework of PanCanRisk. Collaboration in research studies is essential for the advancement of science and beneficial to society. Through voluntary participation we can help broaden the current knowledge about cancer and this information may be useful in the future for other people.

PanCanRisk is searching 2 different profiles:

• Women aged 40-65 years who have had one or more normal mammography results in Women’s Health Dexeus in the last 6 months (BI-RADS 1-2) and who have no personal or family history of cancer at an early age ( provide the latest mammography result).
• Women between 40-65 years old diagnosed with breast cancer with or without a family history of cancer. Patients with a personal or family history of cancer with a identified genetic predisposition may not participate

If your profile corresponds and you are interested in participate, please request an informative visit in the Genomic Medicine Unitby sending an email to or calling +34 932 274 700 indicating your interest in participating in the PanCanRisk / GeneBitsm research projects (Dr. Gabriela Palacios / Dr. Anna Abulí).

For further information, please download the brochure here


Video 1: Welcome – click here

Video 2: Vincenzo L. Pascali “Ethical and legal aspects of giant database storage”– click here

Video 3. Ana Marzo “Legal horizons in the treatment of genomic data” – click here

Video 4. Ferrán Sanz “Data protection in the cloud” – click here

Video 5. Carlos Romeo “Health Big Data and the Cloud: a new challenge for law” – click here

Video 6. Discussion – click here

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