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Journal article

Quantitative analysis of tumour spheroid structure

Abstract:
Progress continues in the field of cancer biology, yet much remains to be unveiled regarding the mechanisms of cancer invasion. In particular, complex biophysical mechanisms enable a tumor to remodel the surrounding extracellular matrix (ECM), allowing cells to invade alone or collectively. Tumor spheroids cultured in collagen represent a simplified, reproducible 3D model system, which is sufficiently complex to recapitulate the evolving organization of cells and interaction with the ECM that occur during invasion. Recent experimental approaches enable high resolution imaging and quantification of the internal structure of invading tumor spheroids. Concurrently, computational modeling enables simulations of complex multicellular aggregates based on first principles. The comparison between real and simulated spheroids represents a way to fully exploit both data sources, but remains a challenge. We hypothesize that comparing any two spheroids requires first the extraction of basic features from the raw data, and second the definition of key metrics to match such features. Here, we present a novel method to compare spatial features of spheroids in 3D. To do so, we define and extract features from spheroid point cloud data, which we simulated using Cells in Silico (CiS), a high-performance framework for large-scale tissue modeling previously developed by us. We then define metrics to compare features between individual spheroids, and combine all metrics into an overall deviation score. Finally, we use our features to compare experimental data on invading spheroids in increasing collagen densities. We propose that our approach represents the basis for defining improved metrics to compare large 3D data sets. Moving forward, this approach will enable the detailed analysis of spheroids of any origin, one application of which is informing in silico spheroids based on their in vitro counterparts. This will enable both basic and applied researchers to close the loop between modeling and experiments in cancer research
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.7554/elife.73020

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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-8753-1538
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Role:
Author
ORCID:
0000-0002-2865-4853
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Role:
Author
ORCID:
0000-0002-9844-6734
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Role:
Author
ORCID:
0000-0003-1317-5988


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Funder identifier:
10.13039/501100000923
Grant:
DP200100177


Publisher:
eLife Sciences Publications
Journal:
eLife More from this journal
Volume:
10
Pages:
e73020
Article number:
e73020
Publication date:
2021-11-29
Acceptance date:
2021-11-26
DOI:
EISSN:
2050-084X
ISSN:
2050-084X


Language:
English
Keywords:
Pubs id:
1219112
Local pid:
pubs:1219112
Source identifiers:
W3214944849
Deposit date:
2026-04-08
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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