Transient transcription factor (OSKM) expression is key towards clinical translation of in vivo cell reprogramming
Reprogramming adult, fully differentiated cells to pluripotency in vivo via Oct3/4 , Sox2 , Klf4 and c‐Myc (OSKM) overexpression has proved feasible in various independent studies and could be used to induce tissue regeneration owing to the proliferative capacity and differentiation potential of the...
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Published in | EMBO molecular medicine Vol. 9; no. 6; pp. 733 - 736 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.06.2017
John Wiley & Sons, Inc EMBO Press John Wiley and Sons Inc Springer Nature |
Subjects | |
Online Access | Get full text |
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Summary: | Reprogramming adult, fully differentiated cells to pluripotency
in vivo
via
Oct3/4
,
Sox2
,
Klf4
and
c‐Myc
(OSKM) overexpression has proved feasible in various independent studies and could be used to induce tissue regeneration owing to the proliferative capacity and differentiation potential of the reprogrammed cells. However, a number of these reports have described the generation of teratomas caused by sustained reprogramming, which precludes the therapeutic translation of this technology. A recent study by the Izpisúa‐Belmonte laboratory described a cyclic regime for short‐term OSKM expression
in vivo
that prevents complete reprogramming to the pluripotent state as well as tumorigenesis. We comment here on this and other studies that provide evidence that
in vivo
OSKM induction can enhance tissue regeneration, while avoiding the feared formation of teratomas. These results could inspire more research to explore the potential of
in vivo
reprogramming in regenerative medicine.
Graphical Abstract
de Lázaro, Cossu and Kostarelos comment on the prospects of short‐term
in vivo
OSKM induction to initiate cell reprogramming and enhance tissue regeneration, while avoiding the threat of generating teratomas. |
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ISSN: | 1757-4676 1757-4684 |
DOI: | 10.15252/emmm.201707650 |