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Concentric Gel System to Study the Biophysical Role of Matrix Microenvironment on 3D Cell Migration
Published on: April 3, 2015
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Second-harmonic generation scattering directionality predicts tumor cell motility in collagen gels
Kathleen A Burke1, Ryan P Dawes2, Mehar K Cheema3
1University of Rochester, Department of Biomedical Engineering, 207 Robert B. Goergen Hall, P.O. Box 270168, Rochester, New York 14627, United States.
Journal of Biomedical Optics
|January 28, 2015
Summary
Second-harmonic generation (SHG) reveals how collagen structure influences tumor cell movement. Changes in collagen
Area of Science:
- Biophysics
- Cancer Biology
- Biomaterials
Background:
- Second-harmonic generation (SHG) quantifies collagen structural changes during tumor metastasis.
- SHG directionality (F/B ratio) correlates with collagen fibril diameter, spacing, and packing disorder.
- Distinct F/B ratios are observed in invasive ductal carcinoma (IDC) tumors with varying metastatic potential.
Purpose of the Study:
- To investigate the direct relationship between collagen microstructure and tumor cell motility.
- To explore how varying SHG F/B ratios in collagen gels affect tumor cell migration.
Main Methods:
- Utilized in vitro collagen gels with controlled F/B ratios.
- Assessed tumor cell migration within these engineered collagen environments.
- Measured total distance traveled, average velocity, and maximum velocity of tumor cells.
Main Results:
- A significant correlation was found between the SHG F/B ratio and tumor cell migration parameters.
- Higher F/B ratios were associated with altered total distance, average, and maximum cell velocities.
- Collagen microstructure directly influences tumor cell locomotion in a controlled setting.
Conclusions:
- Tumor cell motility is directly impacted by the structural properties of the surrounding collagen matrix.
- The SHG F/B ratio serves as a potential biomarker for predicting tumor cell invasiveness.
- Collagen's influence on cell motility may be a key mechanism driving metastasis in IDC.

