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Macropinocytosis of protein is an amino acid supply route in Ras-transformed cells

Author

Listed:
  • Cosimo Commisso

    (New York University School of Medicine)

  • Shawn M. Davidson

    (Massachusetts Institute of Technology)

  • Rengin G. Soydaner-Azeloglu

    (New York University School of Medicine)

  • Seth J. Parker

    (University of California, San Diego, La Jolla, California 92093, USA)

  • Jurre J. Kamphorst

    (Lewis-Sigler Institute for Integrative Genomics, Carl Icahn Laboratory, Princeton University)

  • Sean Hackett

    (Lewis-Sigler Institute for Integrative Genomics, Carl Icahn Laboratory, Princeton University)

  • Elda Grabocka

    (New York University School of Medicine)

  • Michel Nofal

    (Lewis-Sigler Institute for Integrative Genomics, Carl Icahn Laboratory, Princeton University)

  • Jeffrey A. Drebin

    (Hospital of the University of Pennsylvania)

  • Craig B. Thompson

    (Cancer Biology and Genetics Program, Memorial Sloan-Kettering Cancer Center)

  • Joshua D. Rabinowitz

    (Lewis-Sigler Institute for Integrative Genomics, Carl Icahn Laboratory, Princeton University)

  • Christian M. Metallo

    (University of California, San Diego, La Jolla, California 92093, USA)

  • Matthew G. Vander Heiden

    (Massachusetts Institute of Technology
    Dana-Farber Cancer Institute)

  • Dafna Bar-Sagi

    (New York University School of Medicine)

Abstract

Oncogenic Ras has previously been shown to promote macropinocytosis; here it is demonstrated that this process allows tumour cells to use extracellular proteins to generate amino acids necessary to support tumour growth.

Suggested Citation

  • Cosimo Commisso & Shawn M. Davidson & Rengin G. Soydaner-Azeloglu & Seth J. Parker & Jurre J. Kamphorst & Sean Hackett & Elda Grabocka & Michel Nofal & Jeffrey A. Drebin & Craig B. Thompson & Joshua D, 2013. "Macropinocytosis of protein is an amino acid supply route in Ras-transformed cells," Nature, Nature, vol. 497(7451), pages 633-637, May.
  • Handle: RePEc:nat:nature:v:497:y:2013:i:7451:d:10.1038_nature12138
    DOI: 10.1038/nature12138
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    Cited by:

    1. Hui Tu & Zhimeng Wang & Ye Yuan & Xilin Miao & Dong Li & Hu Guo & Yihong Yang & Huaqing Cai, 2022. "The PripA-TbcrA complex-centered Rab GAP cascade facilitates macropinosome maturation in Dictyostelium," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
    2. Edoardo Ratto & S. Roy Chowdhury & Nora S. Siefert & Martin Schneider & Marten Wittmann & Dominic Helm & Wilhelm Palm, 2022. "Direct control of lysosomal catabolic activity by mTORC1 through regulation of V-ATPase assembly," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
    3. Misty Shuo Zhang & Jane Di Cui & Derek Lee & Vincent Wai-Hin Yuen & David Kung-Chun Chiu & Chi Ching Goh & Jacinth Wing-Sum Cheu & Aki Pui-Wah Tse & Macus Hao-Ran Bao & Bowie Po Yee Wong & Carrie Yili, 2022. "Hypoxia-induced macropinocytosis represents a metabolic route for liver cancer," Nature Communications, Nature, vol. 13(1), pages 1-19, December.
    4. Kay Oliver Schink & Kia Wee Tan & Hélène Spangenberg & Domenica Martorana & Marte Sneeggen & Virginie Stévenin & Jost Enninga & Coen Campsteijn & Camilla Raiborg & Harald Stenmark, 2021. "The phosphoinositide coincidence detector Phafin2 promotes macropinocytosis by coordinating actin organisation at forming macropinosomes," Nature Communications, Nature, vol. 12(1), pages 1-17, December.
    5. David Paul & Omer Stern & Yvonne Vallis & Jatinder Dhillon & Andrew Buchanan & Harvey McMahon, 2023. "Cell surface protein aggregation triggers endocytosis to maintain plasma membrane proteostasis," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
    6. Ella N. Hoogenboezem & Shrusti S. Patel & Justin H. Lo & Ashley B. Cavnar & Lauren M. Babb & Nora Francini & Eva F. Gbur & Prarthana Patil & Juan M. Colazo & Danielle L. Michell & Violeta M. Sanchez &, 2024. "Structural optimization of siRNA conjugates for albumin binding achieves effective MCL1-directed cancer therapy," Nature Communications, Nature, vol. 15(1), pages 1-20, December.

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