Open AccessGambogic acid inhibits thioredoxin activity and induces ROS-mediated cell death in castration-resistant prostate cancer
Author(s) -
Hong Pan,
Keith H. Jansson,
Michael L. Beshiri,
JuanJuan Yin,
Lei Fang,
Supreet Agarwal,
Holly M. Nguyen,
Eva Corey,
Ying Zhang,
Jie Liu,
Heng Fan,
Hongsheng Lin,
Kathleen Kelly
Publication year - 2017
Publication title -
oncotarget
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.373
H-Index - 127
ISSN - 1949-2553
DOI - 10.18632/oncotarget.20424
Subject(s) - prostate cancer , gambogic acid , medicine , cancer , cancer research , pten , abiraterone acetate , oncology , androgen deprivation therapy , apoptosis , biology , pi3k/akt/mtor pathway , genetics
Advanced prostate cancer (PrCa) is treated with androgen deprivation therapy, and although there is usually a significant initial response, recurrence arises as castrate resistant prostate cancer (CRPC). New approaches are needed to treat this genetically heterogeneous, phenotypically plastic disease. CRPC with combined homozygous alterations to PTEN and TP53 comprise about 30% of clinical samples. We screened eleven traditional Chinese medicines against a panel of androgen-independent Pten/Tp53 null PrCa-derived cell lines and identified gambogic acid (GA) as a highly potent growth inhibitor. Mechanistic analyses revealed that GA disrupted cellular redox homeostasis, observed as elevated reactive oxygen species (ROS), leading to apoptotic and ferroptotic death. Consistent with this, we determined that GA inhibited thioredoxin, a necessary component of cellular anti-oxidative, protein-reducing activity. In other clinically relevant models, GA displayed submicromolar, growth inhibitory activity against a number of genomically-representative, CRPC patient derived xenograft organoid cultures. Inhibition of ROS with N-acetyl-cysteine partially reversed growth inhibition in CRPC organoids, demonstrating ROS imbalance and implying that GA may have additional mechanisms of action. These data suggest that redox imbalances initiated by GA may be useful, especially in combination therapies, for treating the heterogeneity and plasticity that contributes to the therapeutic resistance of CRPC.