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Updated: Feb 25, 2026

A Preclinical Mouse Model of Osteosarcoma to Define the Extracellular Vesicle-mediated Communication Between Tumor and Mesenchymal Stem Cells
Published on: May 6, 2018
Mechanoresponsive stem cells to target cancer metastases through biophysical cues
Linan Liu1,2,3,4,5,6, Shirley X Zhang1,2,3,4,5,6, Wenbin Liao1,2,3,4,5,6
1Sue and Bill Gross Stem Cell Research Center, 845 Health Sciences Road, University of California, Irvine, Irvine, CA 92697, USA.
Abstract:
Despite decades of effort, little progress has been made to improve the treatment of cancer metastases. To leverage the central role of the mechanoenvironment in cancer metastasis, we present a mechanoresponsive cell system (MRCS) to selectively identify and treat cancer metastases by targeting the specific biophysical cues in the tumor niche in vivo. Our MRCS uses mechanosensitive promoter-driven mesenchymal stem cell (MSC)-based vectors, which selectively home to and target cancer metastases in response to specific mechanical cues to deliver therapeutics to effectively kill cancer cells, as demonstrated in a metastatic breast cancer mouse model. Our data suggest a strong correlation between collagen cross-linking and increased tissue stiffness at the metastatic sites, where our MRCS is specifically activated by the specific cancer-associated mechano-cues. MRCS has markedly reduced deleterious effects compared to MSCs constitutively expressing therapeutics. MRCS indicates that biophysical cues, specifically matrix stiffness, are appealing targets for cancer treatment due to their long persistence in the body (measured in years), making them refractory to the development of resistance to treatment. Our MRCS can serve as a platform for future diagnostics and therapies targeting aberrant tissue stiffness in conditions such as cancer and fibrotic diseases, and it should help to elucidate mechanobiology and reveal what cells "feel" in the microenvironment in vivo.
Insights
A novel mechanoresponsive cell system (MRCS) targets cancer metastases by sensing mechanical cues. This approach offers a promising new strategy for cancer treatment with reduced side effects.
Area of Science:
- Biomedical Engineering
- Cancer Biology
- Mechanobiology
Background:
- Cancer metastasis remains a significant challenge with limited effective treatments.
- The tumor microenvironment's mechanical properties play a crucial role in metastasis.
- Targeting these biophysical cues offers a novel therapeutic avenue.
Purpose of the Study:
- To develop a mechanoresponsive cell system (MRCS) for selective identification and treatment of cancer metastases.
- To leverage specific mechanical cues within the tumor niche for targeted therapy.
- To investigate the potential of targeting matrix stiffness for cancer treatment.
Main Methods:
- Engineered mesenchymal stem cell (MSC)-based vectors with mechanosensitive promoters.
- In vivo testing in a metastatic breast cancer mouse model.
- Analysis of collagen cross-linking and tissue stiffness at metastatic sites.
Main Results:
- MRCS selectively homes to and targets cancer metastases in response to mechanical cues.
- A strong correlation was observed between collagen cross-linking, increased tissue stiffness, and MRCS activation.
- MRCS demonstrated reduced deleterious effects compared to constitutively active MSCs.
Conclusions:
- Biophysical cues, particularly matrix stiffness, are persistent and viable targets for cancer therapy.
- MRCS offers a platform for diagnostics and therapies for conditions like cancer and fibrotic diseases.
- This system advances the understanding of mechanobiology and cellular sensing in vivo.
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