Evidence map›Paper›PMID 30715320›Full record

ArticleGigaScience2019

Modeling genotypes in their microenvironment to predict single- and multi-cellular behavior.

Dimitrios Voukantsis, Kenneth Kahn, Martin Hadley, Rowan Wilson, Francesca M Buffa

Abstract read
In one paragraph

Article in GigaScience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. The many faces of mathematical modelling in oncology.The British journal of radiology · 2019
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Dimitrios VoukantsisComputational Biology and Integrative Genomics, MRC/CRUK Oxford Institute, Departmemt of Oncology, University of Oxford, Old Road Campus, Oxford, Oxfordshire, OX3 7DQ, UK.
Kenneth KahnComputational Biology and Integrative Genomics, MRC/CRUK Oxford Institute, Departmemt of Oncology, University of Oxford, Old Road Campus, Oxford, Oxfordshire, OX3 7DQ, UK.
Martin HadleyAcademic Information Technology Research Team, University of Oxford, 13 Bambury Road, Oxford, Oxfordshire, OX2 6NN, UK.
Rowan WilsonAcademic Information Technology Research Team, University of Oxford, 13 Bambury Road, Oxford, Oxfordshire, OX2 6NN, UK.
Francesca M BuffaComputational Biology and Integrative Genomics, MRC/CRUK Oxford Institute, Departmemt of Oncology, University of Oxford, Old Road Campus, Oxford, Oxfordshire, OX3 7DQ, UK.

Funding

Cancer Research UK 23969Cancer Research UK CBIG:23969
6 · The paper itself

Abstract

A cell's phenotype is the set of observable characteristics resulting from the interaction of the genotype with the surrounding environment, determining cell behavior. Deciphering genotype-phenotype relationships has been crucial to understanding normal and disease biology. Analysis of molecular pathways has provided an invaluable tool to such understanding; however, typically it does not consider the physical microenvironment, which is a key determinant of phenotype. In this study, we present a novel modeling framework that enables the study of the link between genotype, signaling networks, and cell behavior in a three-dimensional microenvironment. To achieve this, we bring together Agent-Based Modeling, a powerful computational modeling technique, and gene networks. This combination allows biological hypotheses to be tested in a controlled stepwise fashion, and it lends itself naturally to model a heterogeneous population of cells acting and evolving in a dynamic microenvironment, which is needed to predict the evolution of complex multi-cellular dynamics. Importantly, this enables modeling co-occurring intrinsic perturbations, such as mutations, and extrinsic perturbations, such as nutrient availability, and their interactions. Using cancer as a model system, we illustrate how this framework delivers a unique opportunity to identify determinants of single-cell behavior, while uncovering emerging properties of multi-cellular growth. This framework is freely available at http://www.microc.org.

Indexed as

Cellular MicroenvironmentCell HypoxiaCell LineageCell ProliferationClonal EvolutionComputer SimulationGene Regulatory NetworksGenotypeHumansMutationSignal TransductionSpheroids, Cellularagent-based modelingexecutable biologygene networksgenotype to phenotypemicroenvironmentmolecular pathwayssignaling networks

Identifiers

PMID30715320
PMCPMC6423375

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.