Spatial biomechanics quantification of the Tumoural MicroEnvironment of a HepG2 spheroids with Magnetic Resonance Elastography

Motivation: The Tumoural-Micro-Environment (TME) is characterized by an increase in stiffness, hence the motivation to consider MR-Elastography for its characterization. Goal(s): We present an experimental setup to locally characterize the biomechanics of cancer cells spheroid embedded in a collagen matrix using Magnetic Resonance Elastography (MRE). Approach: Using MRE at 35 microns resolution, we can locally quantify the biomechanic of a spheroid embedded in a collagen matrix. Results: Comparing the biomechanical properties of a tumour spheroid with an agar spheroid, we show that tumour spheroid modulates their microenvironment within a perimeter of 0.9mmx1.8mm. Impact: Developing 3D culture model, starting from patient's biopsy samples, that is predictive to their in vivo response to treatment, easily applicable could be relevant in the field of tailored medicine. This could spare the patient non-effective chemotherapy exposure or surgery.

Authors

Publication Details

Journal
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Published
2025-09-16
DOI
https://doi.org/10.58530/2025/1957
Primary Topic
Elasticity and Material Modeling
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Spatial biomechanics quantification of the Tumoural MicroEnvironment of a HepG2 spheroids with Magnetic Resonance Elastography

Aurélie Bèaufrere, Maddy Parsons, Adel Hammoutène, Lina Aguilera Munoz et al.
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Elasticity and Material Modeling
article

Spatial biomechanics quantification of the Tumoural MicroEnvironment of a HepG2 spheroids with Magnetic Resonance Elastography

Aurélie Bèaufrere, Maddy Parsons, Adel Hammoutène, Lina Aguilera Munoz, Valérie Paradis, Asma Boumaza, Gabrielle Mangin, Ralph Sinkus, Anne‐Sophie van Schelt, Marguerite Ducamp
article en

Abstract

Motivation: The Tumoural-Micro-Environment (TME) is characterized by an increase in stiffness, hence the motivation to consider MR-Elastography for its characterization. Goal(s): We present an experimental setup to locally characterize the biomechanics of cancer cells spheroid embedded in a collagen matrix using Magnetic Resonance Elastography (MRE). Approach: Using MRE at 35 microns resolution, we can locally quantify the biomechanic of a spheroid embedded in a collagen matrix. Results: Comparing the biomechanical properties of a tumour spheroid with an agar spheroid, we show that tumour spheroid modulates their microenvironment within a perimeter of 0.9mmx1.8mm. Impact: Developing 3D culture model, starting from patient's biopsy samples, that is predictive to their in vivo response to treatment, easily applicable could be relevant in the field of tailored medicine. This could spare the patient non-effective chemotherapy exposure or surgery.

Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Openalex Percentile: Top 76%
Elasticity and Material Modeling
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.