Related Experiment Video
Updated: Jan 31, 2026

Isolation of Cancer Stem Cells From Human Prostate Cancer Samples
Published on: March 14, 2014
Mechanochemical Disruption Suppresses Metastatic Phenotype and Pushes Prostate Cancer Cells toward Apoptosis
Hakm Y Murad1,2, Heng Yu1,2, Daishen Luo1,2
1Department of Biomedical Engineering, Tulane University, New Orleans, Louisiana.
Abstract:
Chemical-based medicine that targets specific oncogenes or proteins often leads to cancer recurrence due to tumor heterogeneity and development of chemoresistance. This challenge can be overcome by mechanochemical disruption of cancer cells via focused ultrasound (FUS) and sensitizing chemical agents such as ethanol. We demonstrate that this disruptive therapy decreases the viability, proliferation rate, tumorigenicity, endothelial adhesion, and migratory ability of prostate cancer cells in vitro. It sensitized the cells to TNFR1-- and Fas--mediated apoptosis and reduced the expression of metastatic markers CD44 and CD29. Using a prostate cancer xenograft model, we observed that the mechanochemical disruption led to complete tumor regression in vivo. This switch to a nonaggressive cell phenotype was caused by ROS and Hsp70 overproduction and subsequent impairment of NFκB signaling. FUS induces mechanical perturbations of diverse cancer cell populations, and its combination with agents that amplify and guide remedial cellular responses can stop lethal cancer progression. IMPLICATIONS: Mechanochemical disruption therapy in which FUS is combined with ethanol can be curative for locally aggressive and castration-resistant prostate cancer.
Insights
Focused ultrasound (FUS) combined with ethanol offers a novel mechanochemical disruption therapy. This approach effectively eliminates prostate cancer cells and achieves complete tumor regression in vivo.
Area of Science:
- Oncology
- Biophysics
- Biochemistry
Background:
- Conventional cancer therapies face challenges like tumor heterogeneity and chemoresistance, leading to recurrence.
- Targeting specific oncogenes or proteins often proves insufficient against aggressive cancers.
Purpose of the Study:
- To investigate the efficacy of mechanochemical disruption using focused ultrasound (FUS) and ethanol for treating prostate cancer.
- To evaluate the therapy's impact on cancer cell viability, proliferation, metastasis, and in vivo tumor regression.
Main Methods:
- Mechanochemical disruption of prostate cancer cells using focused ultrasound (FUS) and ethanol in vitro.
- Assessment of cell viability, proliferation, adhesion, migration, and apoptosis.
- Evaluation of tumor regression in a prostate cancer xenograft model in vivo.
Main Results:
- FUS and ethanol treatment significantly decreased prostate cancer cell viability, proliferation, tumorigenicity, and migration in vitro.
- The therapy sensitized cells to apoptosis and reduced metastatic markers (CD44, CD29).
- Complete tumor regression was observed in vivo, attributed to ROS and Hsp70 overproduction, and NFκB signaling impairment.
Conclusions:
- Mechanochemical disruption therapy combining FUS and ethanol shows potential as a curative treatment for aggressive and castration-resistant prostate cancer.
- This approach offers a non-traditional method to overcome chemoresistance and prevent cancer recurrence.
Related Concept Videos
Apoptosis
Drive-Reduction Theory: Push Theory of Motivation
Cancer Cell Migration through Invadopodia
Adaptive Mechanisms in Cancer Cells
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
Acid Suppressive Drugs for Peptic Ulcer Disease: Antacids
However, this neutralization reaction between...
Background and Environment Affect Phenotype
An example of how genetic background affects phenotype can be seen in horses. The Extension gene in horses is responsible for their coat color. A wild-type gene (EE) produces black pigment in the coat, while a mutant gene (ee) produces red pigment. A...

