Mechanisms Regulating Stemness and Differentiation in Embryonal Carcinoma Cells

Just over ten years have passed since the seminal Takahashi-Yamanaka paper, and while most attention nowadays is on induced, embryonic, and cancer stem cells, much of the pioneering work arose from studies with embryonal carcinoma cells (ECCs) derived from teratocarcinomas. This original work was br...

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Main Authors: Gregory M. Kelly, Mohamed I. Gatie
Format: Article
Language:English
Published: Hindawi Limited 2017-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2017/3684178
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spelling doaj-6083163de24a425b820b5dca9c3e6f742020-11-25T01:06:02ZengHindawi LimitedStem Cells International1687-966X1687-96782017-01-01201710.1155/2017/36841783684178Mechanisms Regulating Stemness and Differentiation in Embryonal Carcinoma CellsGregory M. Kelly0Mohamed I. Gatie1Department of Biology, Molecular Genetics Unit, Western University, London, ON, CanadaDepartment of Biology, Molecular Genetics Unit, Western University, London, ON, CanadaJust over ten years have passed since the seminal Takahashi-Yamanaka paper, and while most attention nowadays is on induced, embryonic, and cancer stem cells, much of the pioneering work arose from studies with embryonal carcinoma cells (ECCs) derived from teratocarcinomas. This original work was broad in scope, but eventually led the way for us to focus on the components involved in the gene regulation of stemness and differentiation. As the name implies, ECCs are malignant in nature, yet maintain the ability to differentiate into the 3 germ layers and extraembryonic tissues, as well as behave normally when reintroduced into a healthy blastocyst. Retinoic acid signaling has been thoroughly interrogated in ECCs, especially in the F9 and P19 murine cell models, and while we have touched on this aspect, this review purposely highlights how some key transcription factors regulate pluripotency and cell stemness prior to this signaling. Another major focus is on the epigenetic regulation of ECCs and stem cells, and, towards that end, this review closes on what we see as a new frontier in combating aging and human disease, namely, how cellular metabolism shapes the epigenetic landscape and hence the pluripotency of all stem cells.http://dx.doi.org/10.1155/2017/3684178
collection DOAJ
language English
format Article
sources DOAJ
author Gregory M. Kelly
Mohamed I. Gatie
spellingShingle Gregory M. Kelly
Mohamed I. Gatie
Mechanisms Regulating Stemness and Differentiation in Embryonal Carcinoma Cells
Stem Cells International
author_facet Gregory M. Kelly
Mohamed I. Gatie
author_sort Gregory M. Kelly
title Mechanisms Regulating Stemness and Differentiation in Embryonal Carcinoma Cells
title_short Mechanisms Regulating Stemness and Differentiation in Embryonal Carcinoma Cells
title_full Mechanisms Regulating Stemness and Differentiation in Embryonal Carcinoma Cells
title_fullStr Mechanisms Regulating Stemness and Differentiation in Embryonal Carcinoma Cells
title_full_unstemmed Mechanisms Regulating Stemness and Differentiation in Embryonal Carcinoma Cells
title_sort mechanisms regulating stemness and differentiation in embryonal carcinoma cells
publisher Hindawi Limited
series Stem Cells International
issn 1687-966X
1687-9678
publishDate 2017-01-01
description Just over ten years have passed since the seminal Takahashi-Yamanaka paper, and while most attention nowadays is on induced, embryonic, and cancer stem cells, much of the pioneering work arose from studies with embryonal carcinoma cells (ECCs) derived from teratocarcinomas. This original work was broad in scope, but eventually led the way for us to focus on the components involved in the gene regulation of stemness and differentiation. As the name implies, ECCs are malignant in nature, yet maintain the ability to differentiate into the 3 germ layers and extraembryonic tissues, as well as behave normally when reintroduced into a healthy blastocyst. Retinoic acid signaling has been thoroughly interrogated in ECCs, especially in the F9 and P19 murine cell models, and while we have touched on this aspect, this review purposely highlights how some key transcription factors regulate pluripotency and cell stemness prior to this signaling. Another major focus is on the epigenetic regulation of ECCs and stem cells, and, towards that end, this review closes on what we see as a new frontier in combating aging and human disease, namely, how cellular metabolism shapes the epigenetic landscape and hence the pluripotency of all stem cells.
url http://dx.doi.org/10.1155/2017/3684178
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