| Literature DB >> 28838843 |
Lucia Kucerova1, Erika Durinikova2, Lenka Toro2, Marina Cihova2, Svetlana Miklikova2, Martina Poturnajova2, Zuzana Kozovska2, Miroslava Matuskova2.
Abstract
Mesenchymal stromal cells (MSCs) were introduced as tumor-targeted vehicles suitable for delivery of the gene-directed enzyme/prodrug therapy more than 10 years ago. Over these years key properties of tumor cells and MSCs, which are crucial for the treatment efficiency, were examined; and there are some critical issues to be considered for the maximum antitumor effect. Moreover, engineered MSCs expressing enzymes capable of activating non-toxic prodrugs achieved long-term curative effect even in metastatic and hard-to-treat tumor types in pre-clinical scenario(s). These gene-modified MSCs are termed prodrug-activating MSCs throughout the text and represent promising approach for further clinical application. This review summarizes major determinants to be considered for the application of the prodrug-activating MSCs in antitumor therapy in order to maximize therapeutic efficiency.Entities:
Keywords: Antitumor treatment; Curative effect; Enzyme/prodrug therapy; Human mesenchymal stromal cells; Metastasis; Solid tumors
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Year: 2017 PMID: 28838843 DOI: 10.1016/j.canlet.2017.08.016
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679