Isoginkgetin, a Natural Biflavonoid Proteasome Inhibitor, Sensitizes Cancer Cells to Apoptosis via Disruption of Lysosomal Homeostasis and Impaired Protein Clearance
Author(s) -
Jessica Tsalikis,
Mena AbdelNour,
Armin Farahvash,
Matthew T. Sorbara,
Stephanie Poon,
Dana J. Philpott,
Stephen E. Girardin
Publication year - 2019
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.00489-18
Subject(s) - proteasome , microbiology and biotechnology , biology , autophagy , protein degradation , programmed cell death , proteasome inhibitor , endoplasmic reticulum associated protein degradation , bortezomib , tfeb , apoptosis , unfolded protein response , endoplasmic reticulum , lysosome , biochemistry , immunology , multiple myeloma , enzyme
Protein degradation pathways are critical for maintaining proper protein dynamics within the cell, and considerable efforts have been made toward the development of therapeutics targeting these catabolic processes. We report here that isoginkgetin, a naturally derived biflavonoid, sensitized cells undergoing nutrient starvation to apoptosis, induced lysosomal stress, and activated the lysosome biogenesis geneTFEB .
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