抄録
Osawa et al. find that accumulation of phosphoethanolamine (PEtn) protects cancer cells under glutamine starvation through the downregulation of PCYT2. Glutamine regulates PE biosynthesis through PCYT2, resulting in pro-tumorigenic metabolite PEtn accumulation. PEtn stimulates the tolerance of cancer cells to starvation, and lowered PCYT2 expression correlates with decreased survival in patients.
本文言語 | English |
---|---|
ページ(範囲) | 89-103.e7 |
ジャーナル | Cell Reports |
巻 | 29 |
号 | 1 |
DOI | |
出版ステータス | Published - 2019 10月 1 |
外部発表 | はい |
ASJC Scopus subject areas
- 生化学、遺伝学、分子生物学(全般)
UN SDG
この成果は、次の持続可能な開発目標に貢献しています
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Phosphoethanolamine Accumulation Protects Cancer Cells under Glutamine Starvation through Downregulation of PCYT2. / Osawa, Tsuyoshi; Shimamura, Teppei; Saito, Kyoko その他.
In: Cell Reports, Vol. 29, No. 1, 01.10.2019, p. 89-103.e7.研究成果: Article › 査読
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TY - JOUR
T1 - Phosphoethanolamine Accumulation Protects Cancer Cells under Glutamine Starvation through Downregulation of PCYT2
AU - Osawa, Tsuyoshi
AU - Shimamura, Teppei
AU - Saito, Kyoko
AU - Hasegawa, Yoko
AU - Ishii, Naoko
AU - Nishida, Miyuki
AU - Ando, Ritsuko
AU - Kondo, Ayano
AU - Anwar, Muyassar
AU - Tsuchida, Rika
AU - Hino, Shinjiro
AU - Sakamoto, Akihisa
AU - Igarashi, Kaori
AU - Saitoh, Kaori
AU - Kato, Keiko
AU - Endo, Keiko
AU - Yamano, Shotaro
AU - Kanki, Yasuharu
AU - Matsumura, Yoshihiro
AU - Minami, Takashi
AU - Tanaka, Toshiya
AU - Anai, Motonobu
AU - Wada, Youichiro
AU - Wanibuchi, Hideki
AU - Hayashi, Mitsuhiro
AU - Hamada, Akinobu
AU - Yoshida, Masayuki
AU - Yachida, Shinichi
AU - Nakao, Mitsuyoshi
AU - Sakai, Juro
AU - Aburatani, Hiroyuki
AU - Shibuya, Masabumi
AU - Hanada, Kentaro
AU - Miyano, Satoru
AU - Soga, Tomoyoshi
AU - Kodama, Tatsuhiko
N1 - Funding Information: We thank the members of the Laboratory for Systems Biology and Medicine and Integrative Nutriomics and Oncology, RCAST, The University of Tokyo. We especially thank Ms. A. Izumi, Dr. G. Nagae (RCAST, The University of Tokyo), Dr. S. Ishikawa (Tokyo Dental and Medical University), Dr. A. Hirao (Kanazawa University), and Dr. S. Kuroda (The University of Tokyo) for helpful discussions. The super-computing resource was provided by the Human Genome Center (The University of Tokyo). This work was supported by a Grant-in-Aid for Young Scientists (A) ( 26710005 , T.O.; 15H05325 , T. Shimamura), a Grant-in-Aid for Scientific Research (B) ( 19H03496 , T.O.), a Grant-in-Aid on Innovative Areas ( 16H01567 , 18H04797 , and 18H04897 , T.O.; 15H05912 , T. Shimamura and S.M.), and a Grant-in-Aid for Challenging Exploratory Research ( 16K14605 and 19K22553 , T.O.; 15K12139 , T. Shimamura) from the Ministry of Education, Culture, Sports, Science and Technology of Japan, Priority Issue on Post-K Computer, Integrated Computational Life Science to Support Personalized and Preventive Medicine ( hp170227 , S.M.); JSPS KAKENHI ( JP16H06276 , H.W.); Takeda Science Foundation (T.O.); Kobayashi Foundation for Cancer Research (T.O.); MSD Life Science Foundation (T.O.); Project for Cancer Research and Therapeutic Evolution (P-CREAT); Practical Research for Innovative Cancer Control ( 16cm0106223h0001 , M.H., H.A., T.K., and T.O.) from the Japan Agency for Medical Research and Development (AMED) (T.K., H.A., and T.O.); Research on Regulatory Science of Pharmaceuticals and Medical Devices ( 18mk0101127h0001 , M.H.); and the AMED-CREST from the AMED (T. Soga; JP18gm0910005j0004 , K.H.). Funding Information: We thank the members of the Laboratory for Systems Biology and Medicine and Integrative Nutriomics and Oncology, RCAST, The University of Tokyo. We especially thank Ms. A. Izumi, Dr. G. Nagae (RCAST, The University of Tokyo), Dr. S. Ishikawa (Tokyo Dental and Medical University), Dr. A. Hirao (Kanazawa University), and Dr. S. Kuroda (The University of Tokyo) for helpful discussions. The super-computing resource was provided by the Human Genome Center (The University of Tokyo). This work was supported by a Grant-in-Aid for Young Scientists (A) (26710005, T.O.; 15H05325, T. Shimamura), a Grant-in-Aid for Scientific Research (B) (19H03496, T.O.), a Grant-in-Aid on Innovative Areas (16H01567, 18H04797, and 18H04897, T.O.; 15H05912, T. Shimamura and S.M.), and a Grant-in-Aid for Challenging Exploratory Research (16K14605 and 19K22553, T.O.; 15K12139, T. Shimamura) from the Ministry of Education, Culture, Sports, Science and Technology of Japan, Priority Issue on Post-K Computer, Integrated Computational Life Science to Support Personalized and Preventive Medicine (hp170227, S.M.); JSPS KAKENHI (JP16H06276, H.W.); Takeda Science Foundation (T.O.); Kobayashi Foundation for Cancer Research (T.O.); MSD Life Science Foundation (T.O.); Project for Cancer Research and Therapeutic Evolution (P-CREAT); Practical Research for Innovative Cancer Control (16cm0106223h0001, M.H. H.A. T.K. and T.O.) from the Japan Agency for Medical Research and Development (AMED) (T.K. H.A. and T.O.); Research on Regulatory Science of Pharmaceuticals and Medical Devices (18mk0101127h0001, M.H.); and the AMED-CREST from the AMED (T. Soga; JP18gm0910005j0004, K.H.). T.O. and T.K. designed the experiments; T.O. T. Shimamura, K. Saito, Y.H. N.I. M. Nishida, A.K. M. Anwar, R.T. A.S. K.I. K. Saitoh, K.K. K.E. S. Yamano, M. Anai, M.H. and M.Y. performed the experiments; T.O. T. Shimamura, S.H. Y.K. Y.M. T.M. T.T. Y.W. H.W. A.H. S. Yachida, M. Nakao, J.S. H.A. M.S. K.H. S.M. T. Soga, and T.K. analyzed and interpreted the data; T.O. wrote the manuscript. The authors declare no competing interests. Publisher Copyright: © 2019 The Author(s)
PY - 2019/10/1
Y1 - 2019/10/1
N2 - Osawa et al. find that accumulation of phosphoethanolamine (PEtn) protects cancer cells under glutamine starvation through the downregulation of PCYT2. Glutamine regulates PE biosynthesis through PCYT2, resulting in pro-tumorigenic metabolite PEtn accumulation. PEtn stimulates the tolerance of cancer cells to starvation, and lowered PCYT2 expression correlates with decreased survival in patients.
AB - Osawa et al. find that accumulation of phosphoethanolamine (PEtn) protects cancer cells under glutamine starvation through the downregulation of PCYT2. Glutamine regulates PE biosynthesis through PCYT2, resulting in pro-tumorigenic metabolite PEtn accumulation. PEtn stimulates the tolerance of cancer cells to starvation, and lowered PCYT2 expression correlates with decreased survival in patients.
KW - PCYT2
KW - PE biosynthesis
KW - amino acids
KW - cancer metabolism
KW - glutamine deprivation
KW - hypoxia
KW - nutrient starvation
KW - phosphoethanolamine
KW - tumor microenvironments
UR - http://www.scopus.com/inward/record.url?scp=85072271823&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85072271823&partnerID=8YFLogxK
U2 - 10.1016/j.celrep.2019.08.087
DO - 10.1016/j.celrep.2019.08.087
M3 - Article
C2 - 31577958
AN - SCOPUS:85072271823
VL - 29
SP - 89-103.e7
JO - Cell Reports
JF - Cell Reports
SN - 2211-1247
IS - 1
ER -