| Literature DB >> 27135648 |
Osamu Sano1, Kenichi Kazetani1, Masaaki Funata1, Yasunori Fukuda1, Junji Matsui1, Hidehisa Iwata1.
Abstract
Lysosomal protein degradation via autophagy strictly regulates cellular protein homoeostasis. Herein we performed high-content screening to identify compounds that inhibit autophagy pathways. We obtained 11 hit compounds and performed cluster analysis using cellular morphological information. Vacuolin-1, which induces the formation of giant vacuoles and is a target unknown compound, clustered with the known PIKfyve inhibitor YM201636. We further confirmed that vacuolin-1 is a potent PIKfyve inhibitor, and we finally concluded that PIKfyve inhibitors are novel chemical tools for regulating autophagy.Entities:
Keywords: PIKfyve; autophagy; vacuolin-1
Mesh:
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Year: 2016 PMID: 27135648 DOI: 10.1002/1873-3468.12195
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124