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Resistance, chemotherapy and predictive biomarkers
Martínez-Balibrea’s Lab

DESCRIPTION

The main objective of our group is based on the identification and analysis of new biomarkers associated with resistance to current colorectal cancer treatment. Our research focuses on the study of the molecular profiles associated with resistance using different preclinical models and the translation of our findings to clinical practice.

Colorectal cancer (CRC), being the most prevalent form of cancer, stands as the second leading cause of cancer-related mortality in Spain. Despite the existence of various preventive campaigns facilitating the early detection of CRC, patients are usually diagnosed at an advanced stage of the disease. Treatment for these patients typically involves a combination of chemotherapy and anti-target drugs, aiming to diminish the tumour burden in order to operate the metastases (significantly extending survival rates) or improve symptomatology prolonging life (and its quality) as much as possible. Despite the significant advancements in the field of oncology, immunotherapies, unfortunately, demonstrate effectiveness in less than 5% of colorectal cancer cases.

One of the main problems in clinical practice is the emergence of treatment resistance, affecting almost all of our treated patients. The primary goal of our group is to understand the underlying mechanisms of this resistance and to identify predictive biomarkers associated with treatment response. Our research efforts are concentrated on the identification of tumour vulnerabilities in order to facilitate the utilization of alternative existing treatments or the development of new chemotherapeutic agent combination.

Our research is focused on the identification of predictive biomarkers to improve treatment selection. To attain this objective, we are investigating specific somatic polymorphisms within genes implicated in pharmacodynamics and pharmacokinetics processes that modulate the efficacy of particular chemotherapeutic drugs or their associated toxicities. Additionally, we are studying tumour gene and/or protein expression patterns derived from colorectal cancer patients’ samples. This analysis aims to decipher potential correlations with chemotherapy resistance, helping us to identify clinical biomarkers essential for treatment selection.

To deeply understand the mechanisms involved in the development of acquired resistance to various anticancer therapies, we developed and implemented in vitro and ex vivo models in our laboratory. Based on these experimental models, we study alterations, using high-throughput techniques, in the profiles of gene and protein expressions, alongside other changes, such as modifications in DNA-methylation patterns, associated with the emergence of resistance subsequent to treatment. This exploration of the molecular landscape helps us to elucidate potential mechanisms responsible for the acquisition of resistance to chemotherapeutics, defining new putative predictive biomarkers that allows us to identify innovative therapeutic intervention capable of reversing this chemoresistance

The most recent projects in which our laboratory is currently involved include:

Modelling immunotherapy response and toxicity in cancer (IMMUNO-model)

PI: Eva Martinez-Balibrea

Funding agency: COST (European Cooperation in Science and Technology) Association
Agency code: CA21135
Start date: 01/10/2022
End date: 31/12/2026

SPOT & HIT: Enabling personalized colorectal cancer management by coupling unified genetic and epigenetic testing to organoidbased treatment screening

Jordi Barretina, coordinator of WP1 and WP3
Funding agency: Ministerio de Ciencia e Innovación
Start date: 01/12/2022
End date: 30/11/2025

Integrating Translational Research in Gastric Cancer. Grupo TTD

Cinta Hierro, team member
Funding agency: Ministerio de Ciencia e Innovación
Start date: 01/01/2023
End date: 31/12/2023 

Systematic analysis of tumor vulnerabilities conferred by chromatin regulators loss in colorectal cancer

PI: Eva Martinez-Balibrea
Funding agency: Instituto de Salud Carlos III (ISCIII)
Agency code: PI20/01183
Start date: 01/01/2021
End date: 31/12/2023

Implementation of a comprehensive translational research platform within the framework of early clinical trials: the INSPECTA project

Eva Martinez-Balibrea, team member
Funding agency: Fundacion Merck Salud
Start date: 2020
End date: 2023

Remodelers of the extracellular matrix: association with lymphocytic infiltration and applicability as markers of response to immunotherapy in colon and rectal cancer

Eva Martinez-Balibrea, team member
Funding agency: Fundación Mutua Madrileña
Start date: 2020
End date: 2023

Degrading Cdk5 for treatment of colorectal cancer

PI: Eva Martinez-Balibrea
Funding agency: Fundación Científica Asociación Española Contra el Cáncer (AECC)
Start date: 01/12/2020
End date: 30/06/2023

Group members

Cristina Queralt Herrero

Researchers

Post Doc

Ferran Grau Leal

Researchers

Pre Doc

Carla Vendrell Ayats

Researchers

Pre Doc

Eva Martinez-Balibrea

Group leaders

Principal Investigator

Marta Domènech

Researchers

Pre Doc

Melanie Giorgi

Support staff

Project Manager

Publications

Epigenetic inactivation of the BRCA1 interactor SRBC and resistance to oxaliplatin in colorectal cancer

26 de November de 2013/in Martínez-Balibrea's Lab/by miguel

J Natl Cancer Inst. 2014 Jan;106(1):djt322. doi: 10.1093/jnci/djt322. Epub 2013 Nov 22. ABSTRACT BACKGROUND: A major problem in cancer chemotherapy is the existence of primary resistance and/or the acquisition of secondary resistance. Many cellular defects contribute to chemoresistance, but epigenetic changes can also be a cause. METHODS: A DNA methylation microarray was used to identify […]

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 miguel2013-11-26 11:00:002013-11-26 11:00:00Epigenetic inactivation of the BRCA1 interactor SRBC and resistance to oxaliplatin in colorectal cancer

Soluble FAS in the prediction of benefit from cetuximab and irinotecan for patients with advanced colorectal cancer

23 de January de 2013/in Martínez-Balibrea's Lab/by miguel

Med Oncol. 2013 Mar;30(1):428. doi: 10.1007/s12032-012-0428-0. Epub 2013 Jan 22. ABSTRACT The FAS/FASL system, comprising membrane-bound (mFAS and mFASL) and soluble forms (sFAS and sFASL), has been related to apoptosis driven by chemotherapy administration. In vitro experiments show chemotherapy upregulating membrane-bound forms, leading to an increase of receptor availability (at 24-72 h) and favoring apoptosis. […]

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 miguel2013-01-23 11:00:002013-01-23 11:00:00Soluble FAS in the prediction of benefit from cetuximab and irinotecan for patients with advanced colorectal cancer

ERCC1 and ERCC2 polymorphisms predict clinical outcomes of oxaliplatin-based chemotherapies in gastric and colorectal cancer: a systemic review and meta-analysis

1 de February de 2011/in Martínez-Balibrea's Lab/by miguel

Clin Cancer Res. 2011 Mar 15;17(6):1632-40. doi: 10.1158/1078-0432.CCR-10-2169. Epub 2011 Jan 28. ABSTRACT PURPOSE: Nucleotide excision repair (NER) modulates platinum-based chemotherapeutic efficacy by removing drug-produced DNA damage. To summarize published data on the association between polymorphisms of NER genes (ERCC1 and ERCC2) and responses to oxaliplatin-based chemotherapies, we carried out a meta-analysis of gastric and […]

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 miguel2011-02-01 11:00:002011-02-01 11:00:00ERCC1 and ERCC2 polymorphisms predict clinical outcomes of oxaliplatin-based chemotherapies in gastric and colorectal cancer: a systemic review and meta-analysis

UGT1A and TYMS genetic variants predict toxicity and response of colorectal cancer patients treated with first-line irinotecan and fluorouracil combination therapy

15 de July de 2010/in Martínez-Balibrea's Lab/by miguel

Br J Cancer. 2010 Aug 10;103(4):581-9. doi: 10.1038/sj.bjc.6605776. Epub 2010 Jul 13. ABSTRACT BACKGROUND: The impact of thymidylate synthase (TYMS) and UDP-glucoronosyltransferase 1A (UGT1A) germline polymorphisms on the outcome of colorectal cancer (CRC) patients treated with irinotecan plus 5-fluorouracil (irinotecan/5FU) is still controversial. Our objective was to define a genetic-based algorithm to select patients to […]

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 miguel2010-07-15 10:00:002010-07-15 10:00:00UGT1A and TYMS genetic variants predict toxicity and response of colorectal cancer patients treated with first-line irinotecan and fluorouracil combination therapy

A proteomic approach links decreased pyruvate kinase M2 expression to oxaliplatin resistance in patients with colorectal cancer and in human cell lines

18 de April de 2009/in Martínez-Balibrea's Lab/by miguel

Mol Cancer Ther. 2009 Apr;8(4):771-8. doi: 10.1158/1535-7163.MCT-08-0882. ABSTRACT We aimed to gain further understanding of the molecular mechanisms involved in oxaliplatin resistance in colorectal cancer by using a proteomic approach. A 5-fold oxaliplatin-resistant cell line, HTOXAR3, was compared with its parental cell line, HT29, using two-dimensional PAGE. Mass spectrometry, Western blot, and real-time quantitative PCR […]

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 miguel2009-04-18 10:00:002009-04-18 10:00:00A proteomic approach links decreased pyruvate kinase M2 expression to oxaliplatin resistance in patients with colorectal cancer and in human cell lines
Page 7 of 9«‹56789›»

Collaborations

Our group proudly participates in the CARE programme of the Institute of Health Research Germans Trias i Pujol (IGTP), as well as the ProCURE programme of the Catalan Institute of Oncology (https://ico.gencat.cat/ca/recerca/Programa-ProCURE/). We are also integral members of the established SGR group, transICOBAD (2021 SGR 01330), under the leadership of Dr Ricard Mesia, who is the Director of B-ARGO and also holds the position of Chair within the Medical Oncology Service at the ICO Badalona. Internationally, Dr Martinez-Balibrea takes on the key role of Secretary within the EORTC Pathobiology Group (https://www.eortc.org/research_field/pathobiology/). Dr Martinez-Balibrea also chairs the prestigious COST Action IMMUNO Model (CA21135) (www.immuno-model.eu)

Martínez-Balibrea's Lab
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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