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Updated: Jan 23, 2026

Exploring the Potential of Mesenchymal Stem Cell Sheet on The Development of Hepatocellular Carcinoma In Vivo
Published on: September 11, 2018
Engineered Mesenchymal Stem Cells for Targeting Solid Tumors: Therapeutic Potential beyond Regenerative Therapy
Shen Cheng1, Susheel Kumar Nethi1, Sneha Rathi1
1Departments of Experimental and Clinical Pharmacology (S.C., S.K.N., B.L., S.P.) and Pharmaceutics (S.R., S.P.), College of Pharmacy, University of Minnesota, Twin Cities, Minnesota.
Mesenchymal stem cells (MSCs) show promise for targeted cancer therapy. This review explores non-genetic methods to enhance MSCs for delivering chemotherapy drugs, overcoming limitations of previous genetic modifications.
Area of Science:
- Biomedical Engineering
- Cancer Therapeutics
- Regenerative Medicine
Background:
- Mesenchymal stem cells (MSCs) possess regenerative potential and tumor-homing capabilities.
- MSCs are explored as cellular vehicles for targeted cancer therapy.
- Previous efforts focused on genetically modified MSCs for protein delivery, facing drug load capacity limitations.
Purpose of the Study:
- To review strategies for non-genetically modifying MSCs.
- To enhance MSCs for targeted delivery of small molecule chemotherapeutic agents.
- To overcome limitations in using MSCs as drug delivery vehicles.
Main Methods:
- Discussion of various non-genetic modification strategies for MSCs.
- Exploitation of MSCs' inherent tumor-tropic and drug-resistant properties.
- Focus on optimizing MSC engineering for drug delivery.
Main Results:
- Non-genetic modifications offer a viable approach for MSC-based drug delivery.
- Enhanced MSCs can improve the targeted delivery of chemotherapeutic agents.
- Addressing molecular mechanisms of tumor tropism is key for efficacy.
Conclusions:
- Non-genetic modification of MSCs is a promising strategy for targeted cancer chemotherapy.
- Optimizing MSCs as drug delivery vehicles requires further research into tumor tropism mechanisms.
- MSCs' inherent properties make them suitable carriers for cytotoxic payloads.
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