About Eloy Francisco Robles Cortes

This author has not yet filled in any details.
So far Eloy Francisco Robles Cortes has created 6 blog entries.

Discovery of a “new molecular trait” shared by myeloma patients

(Pamplona, Spain, August 20, 2020) — A joint research by groups of the EDITOR Accelerator Award have discovered a molecular trait that is shared by myeloma patients.

Multiple myeloma is a greatly heterogeneous disease, both from biological and clinical perspectives. In spite of this heterogeneity, several groups of the EDITOR accelerator award have discovered a molecular trait that is shared by myeloma patients. The study has been led by the groups of Xabier Agirre and Felipe Prosper from the CIMA of Pamplona and Iñaki Martin-Subero from the Hospital Clinic of Barcelona, also with the participation of Jesus San Miguel, coordinator of the EDITOR project. The article, recently published in Genome Research, is entitled “Chromatin activation as a unifying principle underlying pathogenic mechanisms in multiple myeloma”. Using a multi-epigenomics approach and integrative computational analyses as well as detailed functional experiments, the authors identified the existence of a core epigenomic landscape underlying MM pathogenesis. This chromatin landscape is mostly characterized by the widespread activation of regulatory elements that remain inactive in normal cells. Such activation, seems to be mediated by the action of specific TF families, affecting genes particularly involved in preventing cell death associated with cellular stress, such as TXN and PRDM5. As chromatin activation seems to be a feature of myeloma patients as a whole, these findings suggests that drugs reverting this epigenetic process may be appropriate as a backbone treatment for this aggressive disease. (Read more)

Discovery of a “new molecular trait” shared by myeloma patients2020-09-08T06:10:05+00:00

New MDS Subtype Proposed Based on Presence of Genetic Mutation. (Article in English, April 29th 2020)

(WASHINGTON, April 29, 2020) — In a special report published today in the journal Blood, an international working group of experts in myelodysplastic syndromes (MDS) proposes – for the first time – the recognition of a distinct subtype of MDS based on the presence of a nonheritable genetic mutation that causes the disease. The mutation is found in approximately one in every five patients with MDS.

“This study represents an important step forward in the ability to diagnose MDS on the basis of genetic features, and this is paving the way to obtain a diagnosis without the need to analyze bone marrow,” said lead author Luca Malcovati, MD, of the University of Pavia Medical School in Italy. “Patients who carry this genetic variant may benefit from treatment with an approved drug, luspatercept. In addition, other potential new treatments that directly target this genetic mutation are in the early stages of development and may benefit patients in the future.” (Read more)

New MDS Subtype Proposed Based on Presence of Genetic Mutation. (Article in English, April 29th 2020)2020-08-19T13:41:27+00:00

Advanced genomics, design of new animal models and patient sample collection: EDITOR project goals during 2019 (December 22th 2020)

December 2019. EDITOR project, focused on improving early detection and intervention of blood cancers, has completed a year with a positive balance in its forecasts. It started in its kick-off meeting held in January 2019 at Clinica Universidad de Navarra headquarters in Madrid (Spain). During this year the 13 institutions -from Spain, Italy and the United Kingdom- that form part of this international consortium have advanced in the knowledge of monoclonal gammopathies such as multiple myeloma, leukaemia and lymphoma. For that progress, the scientists based the research on the use of the latest techniques in genomic sequencing, the development of new humanized animal models of these diseases, and the compilation of large patient samples.a.

Among the scientific advances of the project, researchers have implemented protocols for advance genomics. Therefore, they used techniques such as RNA-sequencing or massively parallel single-cell RNA-sequencing based on small cell populations selected through high sensitivity fluorescence-activated cell sorting, a specialized type of flow cytometry. “The results obtained with these techniques are changing our understanding of myelomagenesis and clonal heterogeneity, and that could have an impact on the development of new therapeutic strategies,” says Dr Jesús San Miguel, Director of Clinical and Translational Medicine at Universidad de Navarra and the lead investigator. (Read more)

Advanced genomics, design of new animal models and patient sample collection: EDITOR project goals during 2019 (December 22th 2020)2020-05-08T08:56:05+00:00

The EDITOR project Advances in the Time of Coronavirus (March 9th 2020)

March 2020. The Steering Board from the EDITOR project, an international early detection and intervention of blood cancer research, held its third scientific meeting by videoconference.  Clinica Universidad de Navarra (Spain) organised this meeting in which 36 researchers attended. They represented the 13 research institutions from the United Kingdom, Italy and Spain that are part of the project. Also, there were representatives from the financing institutions (CRUK and AECC) and the multiple myeloma patient association. Due to the COVID-19 pandemia the meeting, initially planned to take place in Madrid, was replaced by a virtual meeting with the same agenda.

Dr Jesús San Miguel, Director of Clinical and Translational Medicine at the Universidad de Navarra and the lead investigator, introduced the session remembering the mission of the project and updating the progress achieved during its first year. Among them, he highlighted the design of new tools for cell detection and characterisation, the development of antibodies panels, the establishment of new protocols and the design of improved mouse models. Subsequently, there were sessions dedicated to the advances in each disease. Thus, they were focused on multiple myeloma (MM) or amyloidosis (AL), follicular lymphoma (FL), myelodysplastic syndromes (MDS) and acute myeloid leukaemia (AML). The last presentation was about the development of computational biology systems for the identification of new therapeutic targets and the design of personalised therapies for the treatment of these haematological malignancies. (Read more)

The EDITOR project Advances in the Time of Coronavirus (March 9th 2020)2020-05-08T09:15:23+00:00

Accelerator Award to improve early detection and intervention of blood cancers (Oct. 9th 2018)

BCI researchers are lead members of an international team to be funded by an Accelerator Award, which will bring together scientists from the UK, Spain and Italy in a bid to improve early detection and intervention of blood cancers. The award of £4.8M over 5 years, funded through a partnership between Cancer Research UK (CRUK), AIRC and FC AECC, encourages cross-institutional collaboration to unite resources and expertise to accelerate progress in cancer research.

The Accelerator Award, led by Prof Jesus San Miguel, Director of Clinical and Translational Medicine at the University of Navarra, Spain, will support research into three types of blood cancer: follicular lymphoma, multiple myeloma and acute myeloid leukaemia, with each country acting as a specialist hub (across 13 centres) for one of these diseases. The three cancer types share similar features of progression, and the team hope to develop integrative models of how they evolve from a pre-malignant (or minimal residual disease) stage to malignant disease, and how best to target these cancers at their most vulnerable. (Read more)

Accelerator Award to improve early detection and intervention of blood cancers (Oct. 9th 2018)2020-02-07T12:23:43+00:00

Detecting blood cancers earlier than ever before. CRUK interviewa Dr. Jesús San Miguel (Sept. 13th 2018)

A new international Accelerator Award is funding researchers from the UK, Spain and Italy to improve early detection and intervention of haematological malignancies. The team is working together to develop disease models and produce data for studying blood cancers at an earlier stage. We talked to the lead investigator, Professor Jesus San Miguel – the Director of Clinical and Translational Medicine and Vice-Dean of the Medical Faculty at the University of Navarra – to learn about how they are combining their expertise to accelerate early detection for blood cancers. (Read more)
Detecting blood cancers earlier than ever before. CRUK interviewa Dr. Jesús San Miguel (Sept. 13th 2018)2020-02-07T12:19:02+00:00