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Leukemia and immuno-oncology
Belver’s Lab

DESCRIPTION

Our research is focused on the study of the molecular mechanisms driving leukemia and lymphoma generation, and on the identification of new therapeutic targets that can potentially translate into novel strategies for the treatment of these diseases.

The Leukemia and Immuno-Oncology group focuses its work on two main research lines. On the one hand, the group studies the molecular mechanisms driving oncogenic transformation and progression in Juvenile Myelomonocytic Leukemia (JMML) with the aim of identifying therapeutic targets that can potentially translate into new treatments for these patients. On the other hand, our team is also interested in studying the impact of human papillomavirus (HPV) infection in the development of B-cell lymphoma.

Molecular pathways and targeted therapies in JMML

Juvenile myelomonocytic leukemia (JMML) is an aggressive myeloproliferative neoplasm of early childhood for which hematopoietic stem cell transplantation (HSCT) is currently the only curative treatment. One out of three children diagnosed with JMML succumb to disease. And these numbers are even more dramatic for those patients carrying activating mutations in the PTPN11 gene, which present the most aggressive forms of the disease with a survival rate of only 25%.

JMML presents a low mutational burden in the coding genome, with five canonical mutations in RAS pathway genes (PTPN11, KRAS, NRAS, CBL and NF1) that act as drivers in more than 90% of the patients and only a few described secondary mutations. However, this apparently simple genetic landscape is accompanied by a high phenotypical variability within the patients, which cannot be explained by our current knowledge. Thus, JMML is still an important clinical challenge due to its heterogeneity, difficult diagnosis, poor prognosis, and the lack of alternative treatment options other than HSCT.

To shed light on these questions, our group has set two main goals:

  1. To identify potential functional aberrations in JMML non-coding regulatory elements that can contribute to the pathogenesis of the disease and explain its heterogeneity.
  2. To develop new small-molecule compounds that block the oncogenic effects of PTPN11 mutations as a therapeutic alternative for the treatment of aggressive JMML.

Role of HPV in B-cell lymphoma pathogenesis

HPV infections are the most common sexually transmitted diseases, affecting approximately 80% of all men and women during their lifetime. Interestingly, HPV has been associated to an increased B-cell lymphoma incidence. Moreover, some studies have shown evidence of HPV infection in B-cell lymphoma cells, suggesting that HPV-driven oncogenic effects might directly contribute to B-cell transformation. However, the specific role of HPV in lymphomagenesis remains unknown. The aim of this project is to shed light on the mechanisms underlying the association between HPV and B-cell lymphoma.

Group members

Laura Belver

Group leaders

Group Leader

Sandra Alonso-Moreno

Support staff

Lab manager

Anna Campagnari

Young investigators

PhD student

Alice Debernardi

Young investigators

Postdoctoral fellow

Claudia Fiñana

Young investigators

PhD student

Noel Gómez-Molina

Young investigators

PhD student

Elisabeth Serracanta

Support staff

Research assistant

Publications

Metabolic reprogramming induces resistance to anti-NOTCH1 therapies in T cell acute lymphoblastic leukemia

22 de September de 2015/in Belver's Lab/by miguel

Nat Med. 2015 Oct;21(10):1182-9. doi: 10.1038/nm.3955. Epub 2015 Sep 21. ABSTRACT Activating mutations in NOTCH1 are common in T cell acute lymphoblastic leukemia (T-ALL). Here we identify glutaminolysis as a critical pathway for leukemia cell growth downstream of NOTCH1 and a key determinant of the response to anti-NOTCH1 therapies in vivo. Mechanistically, inhibition of NOTCH1 […]

https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg 0 0 miguel https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg miguel2015-09-22 10:00:002015-09-22 10:00:00Metabolic reprogramming induces resistance to anti-NOTCH1 therapies in T cell acute lymphoblastic leukemia

Non-coding recurrent mutations in chronic lymphocytic leukaemia

23 de July de 2015/in Belver's Lab/by miguel

Nature. 2015 Oct 22;526(7574):519-24. doi: 10.1038/nature14666. Epub 2015 Jul 22. ABSTRACT Chronic lymphocytic leukaemia (CLL) is a frequent disease in which the genetic alterations determining the clinicobiological behaviour are not fully understood. Here we describe a comprehensive evaluation of the genomic landscape of 452 CLL cases and 54 patients with monoclonal B-lymphocytosis, a precursor disorder. […]

https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg 0 0 miguel https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg miguel2015-07-23 10:00:002015-07-23 10:00:00Non-coding recurrent mutations in chronic lymphocytic leukaemia

Therapeutic targeting of HES1 transcriptional programs in T-ALL

19 de March de 2015/in Belver's Lab/by miguel

Blood. 2015 Apr 30;125(18):2806-14. doi: 10.1182/blood-2014-10-608448. Epub 2015 Mar 17. ABSTRACT Oncogenic activation of NOTCH1 signaling plays a central role in the pathogenesis of T-cell acute lymphoblastic leukemia, with mutations on this signaling pathway affecting more than 60% of patients at diagnosis. However, the transcriptional regulatory circuitries driving T-cell transformation downstream of NOTCH1 remain incompletely […]

https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg 0 0 miguel https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg miguel2015-03-19 10:00:002015-03-19 10:00:00Therapeutic targeting of HES1 transcriptional programs in T-ALL

Aberrant cytokine production by nonmalignant cells in the pathogenesis of myeloproliferative tumors and response to JAK inhibitor therapies

10 de March de 2015/in Belver's Lab/by miguel

Cancer Discov. 2015 Mar;5(3):234-6. doi: 10.1158/2159-8290.CD-15-0095. ABSTRACT Kleppe and colleagues use detailed cytokine profiling analyses to investigate the role of aberrant proinflammatory cytokine secretion in the pathogenesis of myeloproliferative neoplasms. Their analyses implicate constitutive activation of STAT3 in both malignant and nonmalignant bone marrow cell populations as a driver of aberrant cytokine secretion and as […]

https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg 0 0 miguel https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg miguel2015-03-10 10:00:002015-03-10 10:00:00Aberrant cytokine production by nonmalignant cells in the pathogenesis of myeloproliferative tumors and response to JAK inhibitor therapies

A NOTCH1-driven MYC enhancer promotes T cell development, transformation and acute lymphoblastic leukemia

8 de September de 2014/in Belver's Lab/by miguel

Nat Med. 2014 Oct;20(10):1130-7. doi: 10.1038/nm.3665. Epub 2014 Sep 7. ABSTRACT Efforts to identify and annotate cancer driver genetic lesions have been focused primarily on the analysis of protein-coding genes; however, most genetic abnormalities found in human cancer are located in intergenic regions. Here we identify a new long range-acting MYC enhancer controlled by NOTCH1 […]

https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg 0 0 miguel https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg miguel2014-09-08 10:00:002014-09-08 10:00:00A NOTCH1-driven MYC enhancer promotes T cell development, transformation and acute lymphoblastic leukemia
Page 4 of 512345

Research Projects

Title: Design of cell therapies based on DNA mimetic peptides for the treatment of patients with Systemic Lupus Erythematosus

Project Number: N/A

PI: Laura Belver

Source of Support: Merck Salud Foundation and FEDER Foundation

Project Start and End Date: 07/2023 – 06/2026

Total Award Amount: 30,000€

Title: Development of new cell therapies for the treatment of patients with Systemic Lupus Erythematosus patients

Project Number: N/A

PI: Laura Belver

Source of Support: FEDER Foundation

Project Start and End Date: 01/2023 – 06/2024

Total Award Amount: 25,000€

Title: Genetics and molecular mechanisms in hematologic malignancies

Project Number: RYC2020-029400-I

PI: Laura Belver

Source of Support: Ramón y Cajal Program – Spanish Ministry of Science and Innovation

Project Start and End Date: 01/2022 – 12/2026

Total Award Amount: 219,250€

Title: Functional impact of enhancer-associated non-coding mutations in Juvenile Myelomonocytic Leukemia

Project Number: PID2020-117645RB-I00

PI: Laura Belver

Source of Support: Spanish Ministry of Science and Innovation

Project Start and End Date: 09/2021 – 08/2024

Total Award Amount: 205,700€

Title: Molecular pathways and targeted therapies in Juvenile Myelomonocytic Leukemia

Project Number: BFero2020.03

PI: Laura Belver

Source of Support: FERO Foundation

Project Start and End Date: 12/2020 – 11/2023

Total Award Amount: 80,000€

Collaborations

Dominique Bonnet (Crick Institute, London)

Kevin Rouault-Pierre (Barts Centre, London)

Hélène Cavé (Hôpital Robert Debré, Paris)

Anna Sureda (Catalan Institute of Oncology, Barcelona)

Laia Alemany (Catalan Institute of Oncology, Barcelona)

Albert Català (Sant Joan de Dèu Hospital, Barcelona)

Antonio Pérez-Martínez (La Paz Hospital, Madrid)

Ana Galera (Virgen de Arrixaca Hospital, Murcia)

Ginés Luengo (Santa Lucía General University Hospital, Cartagena)

Research group photo
Program Against Cancer Therapeutic Resistance

CONTACT US

Campus IDIBELL
(L’Hospitalet del Llobregat)
Hospital Duran i Reynals, Gran Via 199,
L’Hospitalet del Llobregat,
Barcelona 08908
Tel. +34 93 260 7952

Campus IGTP-IJC
(Badalona)
Campus Can Ruti – IGTP – Building Muntanya,
Rd. Can Ruti, Camí de les escoles s/n,
Badalona, Barcelona 08916
Tel. +34 93 554 3069

Campus IDIBGI
(Girona)
Parc Hospitalari Martí i Julià de Salt, Dr. Castany s/n,
Salt, Girona 17190
Tel. +34 872 987 087

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