Gold Nanorod Photothermal Therapy Alters Cell Junctions and Actin Network in Inhibiting Cancer Cell Collective
Yue Wu1, Moustafa R K Ali1, Bin Dong2
1Laser Dynamics Lab, School of Chemistry and Biochemistry , Georgia Institute of Technology , Atlanta , Georgia 30332-0400 , United States.
Abstract:
Most cancer-related deaths come from metastasis. It was recently discovered that nanoparticles could inhibit cancer cell migration. Whereas most researchers focus on single-cell migration, the effect of nanoparticle treatment on collective cell migration has not been explored. Collective migration occurs commonly in many types of cancer metastasis, where a group of cancer cells move together, which requires the contractility of the cytoskeleton filaments and the connection of neighboring cells by the cell junction proteins. Here, we demonstrate that gold nanorods (AuNRs) and the introduction of near-infrared light could inhibit the cancer cell collective migration by altering the actin filaments and cell junctions with significantly triggered phosphorylation changes of essential proteins, using mass spectrometry-based phosphoproteomics. Further observation using super-resolution stochastic optical reconstruction microscopy (STORM) showed the actin cytoskeleton filament bundles were disturbed, which is difficult to differentiate under a normal fluorescence microscope. The decreased expression level of N-cadherin junctions and morphological changes of tight junction protein zonula occludens 2 were also observed. All of these results indicate possible functions of the AuNR treatments in regulating and remodeling the actin filaments and cell junction proteins, which contribute to decreasing cancer cell collective migration.
Insights
Gold nanorods and near-infrared light inhibit collective cancer cell migration by disrupting actin filaments and cell junctions. This nanoparticle treatment offers a novel strategy against metastasis, a major cause of cancer death.
Area of Science:
- Nanotechnology in oncology
- Cancer metastasis research
- Cellular biophysics
Background:
- Metastasis is the primary cause of cancer-related mortality.
- Nanoparticles show potential in inhibiting cancer cell migration.
- The impact of nanoparticles on collective cell migration remains largely unexplored.
Purpose of the Study:
- To investigate the effect of gold nanorods (AuNRs) and near-infrared light on collective cancer cell migration.
- To elucidate the molecular mechanisms underlying nanoparticle-mediated inhibition of collective migration.
Main Methods:
- Utilized gold nanorods (AuNRs) and near-infrared light exposure.
- Employed mass spectrometry-based phosphoproteomics to analyze protein phosphorylation changes.
- Used super-resolution stochastic optical reconstruction microscopy (STORM) to visualize cytoskeletal and junctional alterations.
Main Results:
- AuNRs and near-infrared light significantly inhibited collective cancer cell migration.
- Treatment altered actin filaments and cell junctions, evidenced by protein phosphorylation changes.
- STORM revealed disturbed actin cytoskeleton filament bundles and decreased N-cadherin expression; zonula occludens 2 showed morphological changes.
Conclusions:
- Gold nanorods, activated by near-infrared light, can regulate and remodel actin filaments and cell junction proteins.
- These alterations effectively decrease cancer cell collective migration, suggesting a potential therapeutic strategy against metastasis.
More Related Videos
09:23Inducing Targeted Mild Hyperthermia in Murine Tumor Models through Photothermal Conversion of Near-infrared Light by Intratumoral Gold Nanorods
Published on: October 10, 2025
10:46Preparation and Photoacoustic Analysis of Cellular Vehicles Containing Gold Nanorods
Published on: May 2, 2016
Related Concept Videos
Cancer Cell Migration through Invadopodia
Cell Migration
Cell Migration
Overview of Cell-Cell Junctions
Occluding or Tight...
Cancer Therapies
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
The Role of Actin and Myosin in Non-muscle Cells
