Internet of Things (IoT) technologies have evolved rapidly during the last decade, and many architecture types have been proposed for distributed and interconnected systems. However, most systems are implemented following fragmented approaches for specific application domains, introducing difficulties in providing unified solutions. However, the unification of solutions is an important feature from an IoT perspective. In this paper, we present an IoT platform that supports multiple application layer communication protocols (Representational State Transfer (REST)/HyperText Transfer Protocol (HTTP), Message Queuing Telemetry Transport (MQTT), Advanced Message Queuing Protocol (AMQP), Constrained Application Protocol (CoAP), and Websockets) and that is composed of open-source frameworks (RabbitMQ, Ponte, OM2M, and RDF4J). We have explored a back-end system that interoperates with the various frameworks and offers a single approach for user-access control on IoT data streams and micro-services. The proposed platform is evaluated using its containerized version, being easily deployable on the vast majority of modern computing infrastructures. Its design promotes service reusability and follows a marketplace architecture, so that the creation of interoperable IoT ecosystems with active contributors is enabled. All the platform’s features are analyzed, and we discuss the results of experiments, with the multiple communication protocols being tested when used interchangeably for transferring data. Developing unified solutions using such a platform is of interest to users and developers as they can test and evaluate local instances or even complex applications composed of their own IoT resources before releasing a production version to the marketplace.

Computational systems and methods are often being used in biological research, including the understanding of cancer and the development of treatments. Simulations of tumor growth and its response to different drugs are of particular importance, but also challenging complexity. The main challenges are first to calibrate the simulators so as to reproduce real-world cases, and second, to search for specific values of the parameter space concerning effective drug treatments. In this work, we combine a multi-scale simulator for tumor cell growth and a genetic algorithm (GA) as a heuristic search method for finding good parameter configurations in reasonable time. The two modules are integrated into a single workflow that can be executed in parallel on high performance computing infrastructures. In effect, the GA is used to calibrate the simulator, and then to explore different drug delivery schemes. Among these schemes, we aim to find those that minimize tumor cell size and the probability of emergence of drug resistant cells in the future. Experimental results illustrate the effectiveness and computational efficiency of the approach. K E Y W O R D Scalibration, drug treatment, genetic algorithm, high performance computing, model exploration Charilaos Akasiadis and Miguel Ponce-de-Leon contributed equally to this study. Arnau Montagud, Evangelos Michelioudakis, Alexia Atsidakou, and Elias Alevizos contributed equally to this study. Alexander Artikis, Alfonso Valencia, and Georgios Paliouras contributed equally to this study.

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The emergence of cell resistance in cancer treatment is a complex phenomenon that emerges from the interplay of processes that occur at different scales. For instance, molecular mechanisms and population-level dynamics such as competition and cell–cell variability have been described as playing a key role in the emergence and evolution of cell resistances. Multi-scale models are a useful tool for studying biology at very different times and spatial scales, as they can integrate different processes occurring at the molecular, cellular, and intercellular levels. In the present work, we use an extended hybrid multi-scale model of 3T3 fibroblast spheroid to perform a deep exploration of the parameter space of effective treatment strategies based on TNF pulses. To explore the parameter space of effective treatments in different scenarios and conditions, we have developed an HPC-optimized model exploration workflow based on EMEWS. We first studied the effect of the cells’ spatial distribution in the values of the treatment parameters by optimizing the supply strategies in 2D monolayers and 3D spheroids of different sizes. We later study the robustness of the effective treatments when heterogeneous populations of cells are considered. We found that our model exploration workflow can find effective treatments in all the studied conditions. Our results show that cells’ spatial geometry and population variability should be considered when optimizing treatment strategies in order to find robust parameter sets.

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