S
Sugiko Watanabe
Researcher at Osaka University
Publications - 6
Citations - 1243
Sugiko Watanabe is an academic researcher from Osaka University. The author has contributed to research in topics: DNA damage & Cellular homeostasis. The author has an hindex of 6, co-authored 6 publications receiving 834 citations.
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Journal ArticleDOI
Exosomes maintain cellular homeostasis by excreting harmful DNA from cells
Akiko Takahashi,Ryo Okada,Koji Nagao,Yuka Kawamata,Aki Hanyu,Shin Yoshimoto,Masaki Takasugi,Sugiko Watanabe,Masato T. Kanemaki,Chikashi Obuse,Eiji Hara,Eiji Hara,Eiji Hara +12 more
TL;DR: Results indicate that exosome secretion maintains cellular homeostasis by removing harmful cytoplasmic DNA from cells, and provide valuable new insights into the control of cellularHomeostasis.
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Small extracellular vesicles secreted from senescent cells promote cancer cell proliferation through EphA2
Masaki Takasugi,Ryo Okada,Akiko Takahashi,David Virya Chen,Sugiko Watanabe,Eiji Hara,Eiji Hara +6 more
TL;DR: It is shown that exosome-like small EVs (sEVs) are important mediators of the pro-tumorigenic function of senescent cells, and a novel mechanism of reactive oxygen species (ROS)-regulated cargo sorting into sEVs is critical for the potentially deleterious growth-promoting effect of the senescent cell secretome.
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Impact of senescence-associated secretory phenotype and its potential as a therapeutic target for senescence-associated diseases.
TL;DR: The functional and regulatory network of SASPs toward opening up new possibilities for controlling aging and aging‐associated diseases are discussed.
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Downregulation of cytoplasmic DNases is implicated in cytoplasmic DNA accumulation and SASP in senescent cells
Akiko Takahashi,Tze Mun Loo,Tze Mun Loo,Ryo Okada,Fumitaka Kamachi,Yoshihiro Watanabe,Masahiro Wakita,Sugiko Watanabe,Shimpei Kawamoto,Kenichi Miyata,Glen N. Barber,Naoko Ohtani,Naoko Ohtani,Eiji Hara,Eiji Hara +14 more
TL;DR: It is shown that cytoplasmic accumulation of nuclear DNA plays key roles in the onset of SASP, and the blockage of this pathway prevents SASP in senescent hepatic stellate cells, accompanied by a decline of obesity-associated hepatocellular carcinoma development in mice.
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p16Ink4a and p21Cip1/Waf1 promote tumour growth by enhancing myeloid-derived suppressor cells chemotaxis.
TL;DR: High expression in myeloid-derived suppressor cells stimulates their chemotactic function, favouring tumour progression, and indicates that regulation of Mo-MDSCs chemotaxis is a valuable potential strategy for control of tumour development.