Table 3.
Six Small Molecules Used for Reprogramming
| Abbreviation | Small Molecule | Function in Reprogramming | Target | References |
|---|---|---|---|---|
| A | A-83-01 | promotes reprogramming of human epidermal keratinocytes using OCT4 and KLF4 | (−)TGF-β(smad2) | Yu et al., 2011, Zhu et al., 2010 |
| C | CHIR99021 | combined with parnate results in the reprogramming of human primary keratinocyte transduced with OCT4 and KLF4 | (−)GSK-3β | Yu et al., 2011, Zhu et al., 2010 |
| T | thiazovivin | ROCK inhibitor which dramatically improves the reprogramming efficiency in the presence of PD, Chir, A-83-01, and hLIF | (−)ROCK | Yu et al., 2011 |
| P | cyclic pifithrin-α | suppression or silencing of P53 significantly increased the reprogramming efficiency of human somatic cells | (−)P53 | Hong et al., 2009, Kawamura et al., 2009, Okita et al., 2011 |
| N | sodium butyrate | enhanced miR302/367 cluster, histone H3 acetylation, promoter DNA demethylation, and the expression of endogenous pluripotency-associated genes | (−)HDAC | Mali et al., 2010, Zhu et al., 2010, Zhang and Wu, 2013; |
| PD | PD0325901 | PD serves as a selection strategy when generating iPSCs from virally transduced neural progenitor cells, and contributes to stabilization of the iPSC state. Selectively binds and inhibits MEK, which may result in the inhibition of phosphorylation and activation of MAPK/ERK and the inhibition of tumor cell proliferation | (−)MEK-(+)MAPK/ERK | Yu et al., 2011, Lin et al., 2009, Zhu et al., 2010 |
See also Figure S2.