Prostate Cancer Cells With the AR‐Low and EMT‐High Phenotype Are Vulnerable to NAD+ Synthesis Inhibitors

Our newly established treatment-resistant cell model has the AR-low/EMT-high phenotype, which is clinically associated with enzalutamide resistance in patients. NAPRT-deficiency (NAPRT-low) can be a novel vulnerability associated with the AR-low/EMT-high phenotype and thus can be targeted by NAD+ inhibitors to improve enzalutamide efficacy.

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Publication Details

Journal
The Prostate
Published
2025-12-09
DOI
https://doi.org/10.1002/pros.70100
Primary Topic
Cancer, Lipids, and Metabolism
Type
article
Field-Weighted Citation Impact
0.00
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article

Prostate Cancer Cells With the AR‐Low and EMT‐High Phenotype Are Vulnerable to NAD+ Synthesis Inhibitors

Hyun‐Kyung Ko, Janét Pittsenbarger, David Z. Qian, Changhui Xue et al.
The Prostate
Cancer, Lipids, and Metabolism
article

Prostate Cancer Cells With the AR‐Low and EMT‐High Phenotype Are Vulnerable to NAD+ Synthesis Inhibitors

Hyun‐Kyung Ko, Janét Pittsenbarger, David Z. Qian, Changhui Xue, Lina Gao, Hao Geng, Kasen Shi, Kaiyo Shi, Rebecca Foertsch
article en

Abstract

Our newly established treatment-resistant cell model has the AR-low/EMT-high phenotype, which is clinically associated with enzalutamide resistance in patients. NAPRT-deficiency (NAPRT-low) can be a novel vulnerability associated with the AR-low/EMT-high phenotype and thus can be targeted by NAD+ inhibitors to improve enzalutamide efficacy.

The ProstateVol. 86(4)
Oregon Health & Science University (US)
Openalex Percentile: Top 52%
Cancer, Lipids, and Metabolism
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