TY - JOUR
T1 - Cancer stem cell induction from mouse embryonic stem cells
AU - Seno, Akimasa
AU - Murakami, Chikae
AU - El-Aarag, Bishoy
AU - Iwasaki, Yoshiaki
AU - Ohara, Toshiaki
AU - Seno, Masaharu
N1 - Publisher Copyright:
© 2019, Spandidos Publications. All rights reserved.
PY - 2019/9
Y1 - 2019/9
N2 - 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.
AB - 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.
KW - Cancer stem cell
KW - Conditioned medium
KW - Mouse embryonic stem cells
UR - http://www.scopus.com/inward/record.url?scp=85070702643&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85070702643&partnerID=8YFLogxK
U2 - 10.3892/ol.2019.10614
DO - 10.3892/ol.2019.10614
M3 - Article
AN - SCOPUS:85070702643
SN - 1792-1074
VL - 18
SP - 2756
EP - 2762
JO - Oncology Letters
JF - Oncology Letters
IS - 3
ER -