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...
Autores principales: | , , , , , |
---|---|
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 |