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Tumour resistance in induced pluripotent stem cells derived from naked mole-rats
The naked mole-rat (NMR, Heterocephalus glaber), which is the longest-lived rodent species, exhibits extraordinary resistance to cancer. Here we report that NMR somatic cells exhibit a unique tumour-suppressor response to reprogramming induction. In this study, we generate NMR-induced pluripotent st...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4866046/ https://www.ncbi.nlm.nih.gov/pubmed/27161380 http://dx.doi.org/10.1038/ncomms11471 |
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author | Miyawaki, Shingo Kawamura, Yoshimi Oiwa, Yuki Shimizu, Atsushi Hachiya, Tsuyoshi Bono, Hidemasa Koya, Ikuko Okada, Yohei Kimura, Tokuhiro Tsuchiya, Yoshihiro Suzuki, Sadafumi Onishi, Nobuyuki Kuzumaki, Naoko Matsuzaki, Yumi Narita, Minoru Ikeda, Eiji Okanoya, Kazuo Seino, Ken-ichiro Saya, Hideyuki Okano, Hideyuki Miura, Kyoko |
author_facet | Miyawaki, Shingo Kawamura, Yoshimi Oiwa, Yuki Shimizu, Atsushi Hachiya, Tsuyoshi Bono, Hidemasa Koya, Ikuko Okada, Yohei Kimura, Tokuhiro Tsuchiya, Yoshihiro Suzuki, Sadafumi Onishi, Nobuyuki Kuzumaki, Naoko Matsuzaki, Yumi Narita, Minoru Ikeda, Eiji Okanoya, Kazuo Seino, Ken-ichiro Saya, Hideyuki Okano, Hideyuki Miura, Kyoko |
author_sort | Miyawaki, Shingo |
collection | PubMed |
description | The naked mole-rat (NMR, Heterocephalus glaber), which is the longest-lived rodent species, exhibits extraordinary resistance to cancer. Here we report that NMR somatic cells exhibit a unique tumour-suppressor response to reprogramming induction. In this study, we generate NMR-induced pluripotent stem cells (NMR-iPSCs) and find that NMR-iPSCs do not exhibit teratoma-forming tumorigenicity due to the species-specific activation of tumour-suppressor alternative reading frame (ARF) and a disruption mutation of the oncogene ES cell-expressed Ras (ERAS). The forced expression of Arf in mouse iPSCs markedly reduces tumorigenicity. Furthermore, we identify an NMR-specific tumour-suppression phenotype—ARF suppression-induced senescence (ASIS)—that may protect iPSCs and somatic cells from ARF suppression and, as a consequence, tumorigenicity. Thus, NMR-specific ARF regulation and the disruption of ERAS regulate tumour resistance in NMR-iPSCs. Our findings obtained from studies of NMR-iPSCs provide new insight into the mechanisms of tumorigenicity in iPSCs and cancer resistance in the NMR. |
format | Online Article Text |
id | pubmed-4866046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48660462016-05-24 Tumour resistance in induced pluripotent stem cells derived from naked mole-rats Miyawaki, Shingo Kawamura, Yoshimi Oiwa, Yuki Shimizu, Atsushi Hachiya, Tsuyoshi Bono, Hidemasa Koya, Ikuko Okada, Yohei Kimura, Tokuhiro Tsuchiya, Yoshihiro Suzuki, Sadafumi Onishi, Nobuyuki Kuzumaki, Naoko Matsuzaki, Yumi Narita, Minoru Ikeda, Eiji Okanoya, Kazuo Seino, Ken-ichiro Saya, Hideyuki Okano, Hideyuki Miura, Kyoko Nat Commun Article The naked mole-rat (NMR, Heterocephalus glaber), which is the longest-lived rodent species, exhibits extraordinary resistance to cancer. Here we report that NMR somatic cells exhibit a unique tumour-suppressor response to reprogramming induction. In this study, we generate NMR-induced pluripotent stem cells (NMR-iPSCs) and find that NMR-iPSCs do not exhibit teratoma-forming tumorigenicity due to the species-specific activation of tumour-suppressor alternative reading frame (ARF) and a disruption mutation of the oncogene ES cell-expressed Ras (ERAS). The forced expression of Arf in mouse iPSCs markedly reduces tumorigenicity. Furthermore, we identify an NMR-specific tumour-suppression phenotype—ARF suppression-induced senescence (ASIS)—that may protect iPSCs and somatic cells from ARF suppression and, as a consequence, tumorigenicity. Thus, NMR-specific ARF regulation and the disruption of ERAS regulate tumour resistance in NMR-iPSCs. Our findings obtained from studies of NMR-iPSCs provide new insight into the mechanisms of tumorigenicity in iPSCs and cancer resistance in the NMR. Nature Publishing Group 2016-05-10 /pmc/articles/PMC4866046/ /pubmed/27161380 http://dx.doi.org/10.1038/ncomms11471 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Miyawaki, Shingo Kawamura, Yoshimi Oiwa, Yuki Shimizu, Atsushi Hachiya, Tsuyoshi Bono, Hidemasa Koya, Ikuko Okada, Yohei Kimura, Tokuhiro Tsuchiya, Yoshihiro Suzuki, Sadafumi Onishi, Nobuyuki Kuzumaki, Naoko Matsuzaki, Yumi Narita, Minoru Ikeda, Eiji Okanoya, Kazuo Seino, Ken-ichiro Saya, Hideyuki Okano, Hideyuki Miura, Kyoko Tumour resistance in induced pluripotent stem cells derived from naked mole-rats |
title | Tumour resistance in induced pluripotent stem cells derived from naked mole-rats |
title_full | Tumour resistance in induced pluripotent stem cells derived from naked mole-rats |
title_fullStr | Tumour resistance in induced pluripotent stem cells derived from naked mole-rats |
title_full_unstemmed | Tumour resistance in induced pluripotent stem cells derived from naked mole-rats |
title_short | Tumour resistance in induced pluripotent stem cells derived from naked mole-rats |
title_sort | tumour resistance in induced pluripotent stem cells derived from naked mole-rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4866046/ https://www.ncbi.nlm.nih.gov/pubmed/27161380 http://dx.doi.org/10.1038/ncomms11471 |
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