Vaccinating Against Cancer with Stem Cells
Stem Cells Fight Cancer Cells
Trials of stem cell treatments using mesenchymal stem cells may soon be underway however as researchers in Massachusetts recently demonstrated that genetically modified stem cells were effective at inducing apoptosis (cell death) in cancer cells in the brains of laboratory mice (Sassportas, et al, 2009). The mesenchymal stem cells (MSCs) used in this study were human MSCs and researchers observed that these were resistant to the cytokine tumor necrosis factor apoptosis ligand (TRAIL) which could eliminate gliomas in the brain. The MSCs were then engineered to express secreted recombinant TRAIL which induced caspase-mediated apoptosis in existing glioma cell lines as well as CD133-positive primary glioma cells. What this means, sans jargon, is that the researchers developed a technique where stem cells which can be taken from the fat of adult humans, or indeed the bone marrow, skin, and other areas of the body can be programmed to seek cancer cells in the brain and kickstart a process where these cancer cells die. Stem-cell therapies may, as a result of this study and those mentioned previously, be designed to treat a variety of cancers based on the factors that induce apoptosis in those specific tumor cells.
References
Sasportas LS, Kasmieh R, Wakimoto H, Hingtgen S, van de Water JA, Mohapatra G, Figueiredo JL, Martuza RL, Weissleder R,Shah K., Assessment of therapeutic efficacy and fate of engineered human mesenchymal stem cells for cancer therapy, Proc Natl Acad Sci U S A. 2009 Mar 24;106(12):4822-7. Epub 2009 Mar 5.
Li.Y, Hui.Z, Ren-He.X, Bei.L, Z.Li “Vaccination with Human Pluripotent Stem Cells Generates A Broad Spectrum of Immunological And Clinical Response Against Colon Cancer”, STEM CELLS, 2009, DOI: 10.1002/stem.234
Woll, P.S., Grzywacz, B., et al, 2009, Human embryonic stem cells differentiate into a homogeneous population of natural killer cells with potent in vivo antitumor activity, Published online before print April 13, 2009, doi: 10.1182/blood-2008-06-165225

