Anticancer Gene-engineered MSC-mediated Cancer Cell Death: An Imaging Demonstration

Xu-Yong Sun, Zhuang Chen, Mani R. Moniri, Hong Lu, Long-Jun Dai, Garth L. Warnock

Department of Surgery University of British Columbia Vancouver, Canada.
Institute of Transplant Medicine 303 Hospital of PLA Nanning, Guangxi, China.
Laboratory of Infection and Immunity, Affiliated Hospital of Luzhou Medical College, Luzhou, Sichuan, China.

DOI: 10.4236/eng.2012.410B009                

Abstract

This study was performed to demonstrate the transportation of an engineered MSC-produced intracellular anticancer gene product between mesenchymal stem cell (MSC) and cancer cells.  MSC-mediated anticancer strategy has held great promise owing to MSCs’ capacity of tumor-directed migration and the availability of specific anticancer genes.  All anticancer genes that have been used in previous MSC-mediated anticancer studies were limited in functioning via extracellular mechanisms, mainly because of the restriction by cell membrane to macromolecules including proteins.  In order to apply the majority of potent anticancer genes to the MSC-mediated anticancer system, a specifically designed expression vector which bears an intracellular anticancer gene, PTEN, is utilized to demonstrate the feasibility of the system in cancer therapies.  A transacting activator of transcription (TAT) was introduced into an expression vector followed by a segment for PTEN-RFP fusion protein.  A direct demonstration of PTEN-RFP transportation between MSC and cancer cells was obtained from direct co-cultures.  A marked cancer cell death was observed in indirect co-cultures with conditioned media from PTEN-transfected MSCs.  The demonstration of PTEN-engineered MSC-produced PTEN transportation indicates the feasibility of applying intracellular anticancer gene expression system in MSC-mediated strategies for cancer therapy.

Keywords

Genetic Engineering; Mesenchymal Stem Cells; Gene Therapy; Cancer Therapy; PTEN

Conflicts of Interest

The authors declare no conflicts of interest.

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