News


02/26: Dr. Maas was awarded the Ayuda Postdoctoral AECC 2025 to continue her work studying the exposome impact on early-onset cancer.

02/26: Dr. Seoane was awarded the Ayuda LAB AECC 2025 for the project "De novo subtype definition and characterisation of BRAF-V600E colorectal cancer patients".

12/25: Dr. Maas presented our work on epigenetic signatures of the exposome in early-onset colorectal cancer at the EACR-Mark Foundation Joint Conference and at the AACR Special Conference.

08/25: Check out our new review about epigenetic synthetic lethality as a cancer therapeutic strategy!

06/25: Núria Montalà Palau, a master student from UPF, has started working in the team to explore early cancer prediction with microRNA.

05/25: Our project of BRAF colorectal cancer characterization has been funded by the Fundacion Olga Torres with the Beca "Josep Bombardo Navines" for Consolidated Researchers.

04/25: Our review about exposomal determinants in tumour initiation is out!

04/25: Check out our published new review about multimodal data integration in early-stage breast cancer!

03/25: We welcome Xavi Viñas, a Master Students helping us exploring the epigenetic impact of environmental exposures in lung cancer.

01/25: We welcome Taras Yuziv Duda, our new Bachelor student working on BRAF mutation in Colon Cancer.

Cancer Computational Biology Group webpage @VHIO

About us:

The Cancer Computational Biology group leverages epi(genetic) cancer datasets in order to discover the molecular mechanisms involved with cancer initiation, progression, drug resistance and metastasis in order to improve patient outcomes. We aim to advance insights into the role of chromatin regulatory elements in treatment response and metastasis, develop novel epigenetic synthetic lethality-based therapeutic strategies, improve patient stratification through multi-omics analysis, and identify novel epigenetic biomarkers of treatment response. We have shown how the genes that modify the chromatin structure are associated with chemotherapy resistance in breast cancer (Nature Medicine, 2019). We are interested in understanding how these epigenetic modifications affect drug resistance and how epigenetic drugs can be used to target tumour suppressor genes. We are also interested in machine learning based integration of multi-omic datasets in order to discover new cancer subgroups and biomarkers, and prediction of outcome and drug response. We have participated in multiple international consortia including The Cancer Genome Atlas, Human Tumor Atlas Network, Cancer Target Discovery and Development and most recently AURORA (Metastatic breast cancer multi-omic cohort).

News:

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Ayuda Postdoctoral AECC 2025

We are excited to share that our postdoc, Dr. Silvana Maas, has been awarded the Ayuda Postdoctoral AECC 2025 for her project “Integrating the exposome into the prevention and treatment of the early-onset cancer epidemic.” In this project, we aim to identify modifiable risk factors contributing to the rise in cancer diagnoses in people under 50 by studying the molecular “fingerprints” environmental exposures leave on our DNA. We will investigate how these exposures shape tumor development and whether they can help identify patients who may benefit from more effective therapies using already approved drugs.

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Ayuda LAB AECC 2025

We are excited to share that our project "De novo subtype definition and characterisation of BRAF-V600E colorectal cancer patients" has been awarded €400,000 in funding. Led by Dr. Jose Seoane, and with major contribution of Dr. Lea Lemler, the project will focus on a subgroup of colorectal cancer patients with an exceptionally aggressive form of the disease. We aim to understand why some patients with BRAF-V600E–mutated CRC respond well to targeted therapies, while others show limited or no response. Our ultimate goal is to help move beyond a one-size-fits-all approach and contribute to more personalised treatment strategies for these patients.

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Conference presentations

As the incidence of early-onset cancers increases, both the American and European associations for cancer research organized a conference focusing on early-onset cancers. Dr. Maas presented our work on epigenetic signatures of the exposome in early-onset colorectal cancer at the EACR-Mark Foundation Joint Conference in November in Bergamo, Italy, and last week during the AACR Special Conference in Montreal, Quebec, Canada.

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Our new review

We just published a new review about epigenetic synthetic lethality. In this paper led by Maria Farina-Morillas in collaboration with the Vall d'Hebron Instituto de Reserca, our team explores how synergies of experimental and computational approaches can provide new opportunities for targeted intervention in cancer treatment.

Núria Montalà Palau

A new Master Student

Núria Montalà Palau, a student from the UPF's Bioinformatic for Health Sciences MSC, has join our team. She will work with us for a year, exploring new deep learning techniques for early detection of cancer in serum microRNA.

Beca Navines

Beca "Josep Bombardo Navines"!

The project of BRAF colorectal cancer characterization has been funded by the Fundacion Olga Torres with the Beca "Josep Bombardo Navines" for Consolidated Researchers.
Thank you so much to Fundacion Olga Torres for the support!

Review

Our second review!

Our second review this year has been published, co-led by Silvana CE Maas about the Exposomal determinants of non-genetic plasticity in tumor initiation. You can check the paper here.

Review

A new review!

Our lab just published a review, led by Arnau Llinas and Maria Butjosa. They are exploring the literature about Multimodal data integration in early-stage breast cancer. You can find the paper here.

Review

A new student!

We welcome Xavi Viñas, a Master student helping us exploring the epigenetic impact of environmental exposures in lung cancer.

Review

A new student!

We welcome Taras Yuziv Duda, our new Bachelor student working on BRAF mutation in Colon Cancer, specifically the BRAF V600E mutation. By comparing the transcriptional programs between BRAFV600E and BRAF nonV600E, he’s trying to figure out why the nonV600E type has a better prognosis than V600E. After, he will also delve deeper in the transcription factor activity behind each mutation type.

Our founders: