Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2078266 | Cell Stem Cell | 2009 | 12 Pages |
Abstract
SummaryThe proliferative capacity of pluripotent stem cells and their progeny brings a unique aspect to therapeutics, in that once a transplant is initiated the therapist no longer has control of the therapy. In the context of the recent FDA approval of a human ESC trial and report of a neuronal-stem-cell-derived tumor in a human trial, strategies need to be developed to control wayward pluripotent stem cells. Here, we focus on one approach: direct genetic modification of the cells prior to transplantation with genes that can prevent the adverse events and/or eliminate the transplanted cells and their progeny.
Related Topics
Life Sciences
Biochemistry, Genetics and Molecular Biology
Biotechnology
Authors
Maija Kiuru, Julie L. Boyer, Timothy P. O'Connor, Ronald G. Crystal,