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Published on: December 13, 2018
Multi-walled nanotubes for cellular reprogramming of cancer
Elizabeth M Wailes1, Nicole H Levi-Polyachenko1
1Department of Plastic and Reconstructive Surgery, Wake Forest University School of Medicine, Winston Salem, NC, USA; Virginia Tech-Wake Forest School of Biomedical Engineering and Sciences, Wake Forest University, Winston Salem, NC, USA.
Multi-walled nanotubes (MWNT) show promise for treating triple-negative breast cancer. These nanotubes restricted cancer cell invasion and migration in a 3D collagen gel model, offering a potential new therapeutic strategy.
Area of Science:
- Biomaterials Science
- Cancer Biology
- Nanotechnology
Background:
- Triple-negative breast cancer (TNBC) is an aggressive subtype lacking targeted therapies.
- Tumor behavior is influenced by the tumor microenvironment, including stromal interactions.
- Mechanical influences on cancer cells are an emerging area of therapeutic interest.
Purpose of the Study:
- To investigate the effects of multi-walled nanotubes (MWNT) on triple-negative breast cancer cell behavior within a 3D collagen gel model.
- To assess MWNT's impact on cancer cell contraction, invasion, viability, MMP-9 expression, and migration.
- To evaluate MWNT as a potential therapeutic agent for TNBC.
Main Methods:
- Co-culture of MDA-MB-231 breast cancer cells and mesenchymal cells within 3D collagen gels.
- Introduction of multi-walled nanotubes (MWNT) into the collagen gel matrix.
- Quantification of cancer cell contraction, invasion, viability, MMP-9 expression, and migration.
Main Results:
- MWNT significantly restricted breast cancer cell contraction, invasion, and migration.
- MWNT did not impede the function of associated mesenchymal cells.
- MWNT treatment reduced MMP-9 expression in cancer cells.
Conclusions:
- MWNT-collagen gels demonstrate potential for cellular reprogramming of triple-negative breast cancer cells.
- MWNTs offer a novel therapeutic approach by modulating mechanical influences on cancer cells.
- Further investigation of MWNTs as a therapeutic agent for TNBC is warranted.
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