Cargando…

Cancer stem cell induction from mouse embryonic stem cells

Although cancers are often removed by surgery and treated by chemotherapy and/or radiation therapies, they often reoccur following treatment due to the presence of resistant residual cells such as cancer stem cells (CSCs). CSCs are characterized by their self-renewal, pluripotency, and tumorigenicit...

Descripción completa

Detalles Bibliográficos
Autores principales: Seno, Akimasa, Murakami, Chikae, El-Aarag, Bishoy, Iwasaki, Yoshiaki, Ohara, Toshiaki, Seno, Masaharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6676632/
https://www.ncbi.nlm.nih.gov/pubmed/31452753
http://dx.doi.org/10.3892/ol.2019.10614
_version_ 1783440802995765248
author Seno, Akimasa
Murakami, Chikae
El-Aarag, Bishoy
Iwasaki, Yoshiaki
Ohara, Toshiaki
Seno, Masaharu
author_facet Seno, Akimasa
Murakami, Chikae
El-Aarag, Bishoy
Iwasaki, Yoshiaki
Ohara, Toshiaki
Seno, Masaharu
author_sort Seno, Akimasa
collection PubMed
description Although cancers are often removed by surgery and treated by chemotherapy and/or radiation therapies, they often reoccur following treatment due to the presence of resistant residual cells such as cancer stem cells (CSCs). CSCs are characterized by their self-renewal, pluripotency, and tumorigenicity properties, and are promising therapeutic targets for the complete therapy of cancers; however, the number of CSCs in cancer tissue is typically too small to investigate fully. We have previously reported that CSCs could be established from induced pluripotent stem cells (iPSCs) using a conditioned medium during cancer cell culture. In the present study, mouse embryonic stem cells (mESCs) were observed to be converted to CSCs (mES-CSCs). This demonstrated that CSC induction does not exclusively occur following gene editing in somatic cells, and that conditioned medium from cancer cells may contain factors that can induce CSCs. Therefore, not only iPSCs but also mESCs, were demonstrated to be able to produce CSCs as one of the potentials of pluripotency of stem cells, suggesting that the conversion to CSCs is not specific to iPSCs. The resultant mES-CSCs would be also useful to generate tissue specific cancers and these naturally occurring cancers can contribute to drug screenings, but also undergo further investigation in order to reveal cancer mechanisms.
format Online
Article
Text
id pubmed-6676632
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-66766322019-08-26 Cancer stem cell induction from mouse embryonic stem cells Seno, Akimasa Murakami, Chikae El-Aarag, Bishoy Iwasaki, Yoshiaki Ohara, Toshiaki Seno, Masaharu Oncol Lett Articles Although cancers are often removed by surgery and treated by chemotherapy and/or radiation therapies, they often reoccur following treatment due to the presence of resistant residual cells such as cancer stem cells (CSCs). CSCs are characterized by their self-renewal, pluripotency, and tumorigenicity properties, and are promising therapeutic targets for the complete therapy of cancers; however, the number of CSCs in cancer tissue is typically too small to investigate fully. We have previously reported that CSCs could be established from induced pluripotent stem cells (iPSCs) using a conditioned medium during cancer cell culture. In the present study, mouse embryonic stem cells (mESCs) were observed to be converted to CSCs (mES-CSCs). This demonstrated that CSC induction does not exclusively occur following gene editing in somatic cells, and that conditioned medium from cancer cells may contain factors that can induce CSCs. Therefore, not only iPSCs but also mESCs, were demonstrated to be able to produce CSCs as one of the potentials of pluripotency of stem cells, suggesting that the conversion to CSCs is not specific to iPSCs. The resultant mES-CSCs would be also useful to generate tissue specific cancers and these naturally occurring cancers can contribute to drug screenings, but also undergo further investigation in order to reveal cancer mechanisms. D.A. Spandidos 2019-09 2019-07-15 /pmc/articles/PMC6676632/ /pubmed/31452753 http://dx.doi.org/10.3892/ol.2019.10614 Text en Copyright: © Seno et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Articles
Seno, Akimasa
Murakami, Chikae
El-Aarag, Bishoy
Iwasaki, Yoshiaki
Ohara, Toshiaki
Seno, Masaharu
Cancer stem cell induction from mouse embryonic stem cells
title Cancer stem cell induction from mouse embryonic stem cells
title_full Cancer stem cell induction from mouse embryonic stem cells
title_fullStr Cancer stem cell induction from mouse embryonic stem cells
title_full_unstemmed Cancer stem cell induction from mouse embryonic stem cells
title_short Cancer stem cell induction from mouse embryonic stem cells
title_sort cancer stem cell induction from mouse embryonic stem cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6676632/
https://www.ncbi.nlm.nih.gov/pubmed/31452753
http://dx.doi.org/10.3892/ol.2019.10614
work_keys_str_mv AT senoakimasa cancerstemcellinductionfrommouseembryonicstemcells
AT murakamichikae cancerstemcellinductionfrommouseembryonicstemcells
AT elaaragbishoy cancerstemcellinductionfrommouseembryonicstemcells
AT iwasakiyoshiaki cancerstemcellinductionfrommouseembryonicstemcells
AT oharatoshiaki cancerstemcellinductionfrommouseembryonicstemcells
AT senomasaharu cancerstemcellinductionfrommouseembryonicstemcells