Published online Apr 26, 2015. doi: 10.4252/wjsc.v7.i3.541
Peer-review started: August 1, 2014
First decision: September 4, 2014
Revised: January 10, 2015
Accepted: January 18, 2015
Article in press: January 20, 2015
Published online: April 26, 2015
Processing time: 265 Days and 22.6 Hours
Induced pluripotent stem cells (iPSCs) have been the focal point of ever increasing interest and scrutiny as they hold the promise of personalized regenerative medicine. However, creation of iPSCs is an inefficient process that requires forced expression of potentially oncogenic proteins. In order to unlock the full potential of iPSCs, both for basic and clinical research, we must broaden our search for more reliable ways of inducing pluripotency in somatic cells. This review surveys an area of reprogramming that does not receive as much focus, barriers to reprogramming, in the hope of stimulating new ideas and approaches towards developing safer and more efficient methods of reprogramming. Better methods of iPSC creation will allow for more reliable disease modeling, better basic research into the pluripotent state and safer iPSCs that can be used in a clinical setting.
Core tip: This review addresses an underappreciated aspect of cellular reprogramming, repressors of reprograming. We review current literature focusing on inhibitors that modify cellular reprogramming.