The MAO inhibitors phenelzine and clorgyline revert enzalutamide resistance in castration resistant prostate cancer.
Keliang WangJie LuoShuyuan YehBosen YouJia-Lin MengPhilip ChangYuanjie NiuGonghui LiChangxue LuYezi ZhuEmmanuel S AntonarakisJun LuoChi-Ping HuangWanhai XuChawnshang ChangPublished in: Nature communications (2020)
The antiandrogen enzalutamide (Enz) has improved survival in castration resistant prostate cancer (CRPC) patients. However, most patients eventually develop Enz resistance that may involve inducing the androgen receptor (AR) splicing variant 7 (ARv7). Here we report that high expression of monoamine oxidase-A (MAO-A) is associated with positive ARv7 detection in CRPC patients following Enz treatment. Targeting MAO-A with phenelzine or clorgyline, the FDA-approved drugs for antidepression, resensitize the Enz resistant (EnzR) cells to Enz treatment and further suppress EnzR cell growth in vitro and in vivo. Our findings suggest that Enz-increased ARv7 expression can transcriptionally enhance MAO-A expression resulting in Enz resistance via altering the hypoxia HIF-1α signals. Together, our results show that targeting the Enz/ARv7/MAO-A signaling with the antidepressants phenelzine or clorgyline can restore Enz sensitivity to suppress EnzR cell growth, which may indicate that these antidepression drugs can overcome the Enz resistance to further suppress the EnzR CRPC.
Keyphrases
- end stage renal disease
- ejection fraction
- newly diagnosed
- poor prognosis
- prostate cancer
- chronic kidney disease
- peritoneal dialysis
- prognostic factors
- long non coding rna
- drug delivery
- induced apoptosis
- major depressive disorder
- endothelial cells
- endoplasmic reticulum stress
- quantum dots
- smoking cessation
- real time pcr