Plasma membrane V-ATPase controls oncogenic RAS-induced macropinocytosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41586-019-1831-x.pdf
Reference37 articles.
1. Commisso, C. et al. Macropinocytosis of protein is an amino acid supply route in Ras-transformed cells. Nature 497, 633–637 (2013).
2. Kamphorst, J. J. et al. Human pancreatic cancer tumors are nutrient poor and tumor cells actively scavenge extracellular protein. Cancer Res. 75, 544–553 (2015).
3. Fennell, M., Commisso, C., Ramirez, C., Garippa, R. & Bar-Sagi, D. High-content, full genome siRNA screen for regulators of oncogenic HRAS-driven macropinocytosis. Assay Drug Dev. Technol. 13, 347–355 (2015).
4. Stransky, L., Cotter, K. & Forgac, M. The function of v-ATPases in cancer. Physiol. Rev. 96, 1071–1091 (2016).
5. Furuchi, T., Aikawa, K., Arai, H. & Inoue, K. Bafilomycin A1, a specific inhibitor of vacuolar-type H+-ATPase, blocks lysosomal cholesterol trafficking in macrophages. J. Biol. Chem. 268, 27345–27348 (1993).
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