MAST: a hybrid Multi-Agent Spatio-Temporal model of tumor microenvironment informed using a data-driven approach

Author:

Cesaro Giulia1ORCID,Milia Mikele1ORCID,Baruzzo Giacomo1ORCID,Finco Giovanni1ORCID,Morandini Francesco1ORCID,Lazzarini Alessio1,Alotto Piergiorgio2,da Cunha Carvalho de Miranda Noel Filipe3,Trajanoski Zlatko4,Finotello Francesca456,Di Camillo Barbara17ORCID

Affiliation:

1. Department of Information Engineering, University of Padova , 35131 Padova, Italy

2. Department of Industrial Engineering, University of Padova , 35131 Padova, Italy

3. Department of Pathology, Leiden University Medical Center , 2300 RC Leiden, The Netherlands

4. Biocenter, Institute of Bioinformatics, Medical University of Innsbruck , 6020 Innsbruck, Austria

5. Institute of Molecular Biology, University Innsbruck , 6020 Innsbruck, Austria

6. Digital Science Center (DiSC), University Innsbruck , 6020 Innsbruck, Austria

7. Department of Comparative Biomedicine and Food Science, University of Padova , 35020 Padova, Italy

Abstract

Abstract Motivation Recently, several computational modeling approaches, such as agent-based models, have been applied to study the interaction dynamics between immune and tumor cells in human cancer. However, each tumor is characterized by a specific and unique tumor microenvironment, emphasizing the need for specialized and personalized studies of each cancer scenario. Results We present MAST, a hybrid Multi-Agent Spatio-Temporal model which can be informed using a data-driven approach to simulate unique tumor subtypes and tumor–immune dynamics starting from high-throughput sequencing data. It captures essential components of the tumor microenvironment by coupling a discrete agent-based model with a continuous partial differential equations-based model. The application to real data of human colorectal cancer tissue investigating the spatio-temporal evolution and emergent properties of four simulated human colorectal cancer subtypes, along with their agreement with current biological knowledge of tumors and clinical outcome endpoints in a patient cohort, endorse the validity of our approach. Availability and implementation MAST, implemented in Python language, is freely available with an open-source license through GitLab (https://gitlab.com/sysbiobig/mast), and a Docker image is provided to ease its deployment. The submitted software version and test data are available in Zenodo at https://dx.doi.org/10.5281/zenodo.7267745. Supplementary information Supplementary data are available at Bioinformatics Advances online.

Funder

PROACTIVE 2017

Department of Information Engineering, University of Padova

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Embryology,Anatomy

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