Synthetic lethality by targeting the RUVBL1/2-TTT complex in mTORC1-hyperactive cancer cells

  • Seung Ho Shin
    The Hormel Institute, University of Minnesota, Austin, MN 55912, USA.
  • Ji Su Lee
    Division of Bioengineering, Incheon National University, Incheon 22012, Republic of Korea.
  • Jia-Min Zhang
    Massachusetts General Hospital Cancer Center, Building 149 13th Street, Charlestown, MA 02129, USA.
  • Sungbin Choi
    Division of Bioengineering, Incheon National University, Incheon 22012, Republic of Korea.
  • Zarko V. Boskovic
    Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
  • Ran Zhao
    School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
  • Mengqiu Song
    School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
  • Rui Wang
    School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
  • Jie Tian
    School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
  • Mee-Hyun Lee
    School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
  • Jae Hwan Kim
    Department of Agricultural Biotechnology, Seoul National University, Seoul 08826, Korea.
  • Minju Jeong
    Department of Agricultural Biotechnology, Seoul National University, Seoul 08826, Korea.
  • Jung Hyun Lee
    Division of Dermatology, Department of Medicine, University of Washington, Seattle, WA 98109, USA.
  • Michael Petukhov
    Petersburg Nuclear Physics Institute named after B.P. Konstantinov, NRC "Kurchatov Institute", Gatchina, Russia.
  • Sam W. Lee
    Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA 02129, USA.
  • Sang Gyun Kim
    Department of Cell Biology, Harvard Medical School, 240 Longwood Ave, Boston, MA 02115, USA.
  • Lee Zou
    Massachusetts General Hospital Cancer Center, Building 149 13th Street, Charlestown, MA 02129, USA.
  • Sanguine Byun
    Division of Bioengineering, Incheon National University, Incheon 22012, Republic of Korea.

抄録

<jats:p>Cancer cells with high mTORC1 activity rely on the RUVBL1/2-TTT pathway for survival, thereby providing a therapeutic window.</jats:p>

収録刊行物

  • Science Advances

    Science Advances 6 (31), 1-, 2020-07-31

    American Association for the Advancement of Science (AAAS)

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