Evidence map›Paper›PMID 29452382›Full record

ArticleMathematical medicine and biology : a journal of the IMA2019

Simulated ablation for detection of cells impacting paracrine signalling in histology analysis.

Jake P Taylor-King, Etienne Baratchart, Andrew Dhawan, Elizabeth A Coker, Inga Hansine Rye, Hege Russnes, S Jon Chapman, David Basanta, Andriy Marusyk

Open access · greenAbstract read
In one paragraph

Article in Mathematical medicine and biology : a journal of the IMA, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. Article
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

9 authors.

Jake P Taylor-KingMathematical Institute, University of Oxford, Oxford, UK.
Etienne BaratchartDepartment of Integrated Mathematical Oncology, Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Andrew DhawanDepartment of Oncology, University of Oxford, Oxford, UK.
Elizabeth A CokerCancer Research UK Cancer Therapeutics Unit, The Institute of Cancer Research, London, UK.
Inga Hansine RyeDepartment of Genetics, Institute for Cancer Research, Oslo University Hospital Radiumhospitalet, Oslo, Norway.
Hege RussnesDepartment of Genetics, Institute for Cancer Research, Oslo University Hospital Radiumhospitalet, Oslo, Norway.
S Jon ChapmanMathematical Institute, University of Oxford, Oxford, UK.
David BasantaDepartment of Integrated Mathematical Oncology, Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Andriy MarusykDepartment of Cancer Imaging and Metabolism, Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.

Funding

Multiscale Modeling of Bone Environment Responses to Metastatic Prostate CancerU01CA202958 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI BASANTA GUTIERREZ, DAVID, LYNCH, CONOR C · 2016 to 2020
$3.3M
NCI NIH HHS U01 CA202958
6 · The paper itself

Abstract

Intra-tumour phenotypic heterogeneity limits accuracy of clinical diagnostics and hampers the efficiency of anti-cancer therapies. Dealing with this cellular heterogeneity requires adequate understanding of its sources, which is extremely difficult, as phenotypes of tumour cells integrate hardwired (epi)mutational differences with the dynamic responses to microenvironmental cues. The later comes in form of both direct physical interactions, as well as inputs from gradients of secreted signalling molecules. Furthermore, tumour cells can not only receive microenvironmental cues, but also produce them. Despite high biological and clinical importance of understanding spatial aspects of paracrine signaling, adequate research tools are largely lacking. Here, a partial differential equation (PDE)-based mathematical model is developed that mimics the process of cell ablation. This model suggests how each cell might contribute to the microenvironment by either absorbing or secreting diffusible factors, and quantifies the extent to which observed intensities can be explained via diffusion-mediated signalling. The model allows for the separation of phenotypic responses to signalling gradients within tumour microenvironments from the combined influence of responses mediated by direct physical contact and hardwired (epi)genetic differences. The method is applied to a multi-channel immunofluorescence in situ hybridisation (iFISH)-stained breast cancer histological specimen, and correlations are investigated between: HER2 gene amplification, HER2 protein expression and cell interaction with the diffusible microenvironment. This approach allows partial deconvolution of the complex inputs that shape phenotypic heterogeneity of tumour cells and identifies cells that significantly impact gradients of signalling molecules.

Indexed as

Models, BiologicalBreast NeoplasmsCell Line, TumorComputer SimulationErb-b2 Receptor Tyrosine KinasesFemaleGene AmplificationHistological TechniquesHumansIn Situ Hybridization, FluorescenceMathematical ConceptsMutationParacrine CommunicationSignal TransductionTumor MicroenvironmentERBB2 protein, humanErb-b2 Receptor Tyrosine Kinasescancerhistologyimage analysisparacrinesignalling

Identifiers

PMID29452382
PMCPMC7197102
OpenAlexW2605927275

What OpenQuestion holds

Textmetadata
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Read underepoch 390

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.