ID | 112460 |
Author |
Miyawaki, Shingo
Hokkaido University|Keio University
Kawamura, Yoshimi
Hokkaido University
Oiwa, Yuki
Hokkaido University
Shimizu, Atsushi
Iwate Medical University
Hachiya, Tsuyoshi
Iwate Medical University
Bono, Hidemasa
Research Organization of Information and Systems
Koya, Ikuko
Keio University
Okada, Yohei
Keio University|Aichi Medical University
Kimura, Tokuhiro
Yamaguchi University
Tsuchiya, Yoshihiro
Hoshi University
Suzuki, Sadafumi
Keio University
Onishi, Nobuyuki
Keio University
Kuzumaki, Naoko
Keio University|Hoshi University
Matsuzaki, Yumi
Shimane University
Narita, Minoru
Hoshi University
Ikeda, Eiji
Yamaguchi University
Okanoya, Kazuo
The University of Tokyo
Seino, Ken-ichiro
Hokkaido University
Saya, Hideyuki
Keio University
Okano, Hideyuki
Keio University
Miura, Kyoko
Hokkaido University|Keio University|Japan Science and Technology Agency
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Content Type |
Journal Article
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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.
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Journal Title |
Nature Communications
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ISSN | 20411723
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NCID | AA12645905
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Publisher | Springer Nature
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Volume | 7
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Start Page | 11471
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Published Date | 2016-05-10
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Remark | Supplementary Information : ncomms_7_11471_s1.pdf
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Rights | 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/
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DOI (Published Version) | |
URL ( Publisher's Version ) | |
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language |
eng
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TextVersion |
Publisher
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departments |
Institute of Advanced Medical Sciences
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