International Journal of Biological SciencesCancer BiologyPeer-reviewed journal article
NNMT drives innate sensitivity to NAMPT inhibition in YAP-dependent stem-like/ mesenchymal prostate cancer
Ágata Sofia Assunção CarreiraiD, Marianna CiuffredaiD, Nathakan ThongoniD, Charles M. Haughey, Adam PickardiD, Sharon L. EddieiD, Rebecca E. SteeleiD, Elena Cerri, Romina BelliiD, Daniele PeroniiD, Elisa FaceniD, Irene CaffaiD, Moustafa S. GhanemiD, Alessio NencioniiD, Andrea LunardiiD, Toma TebaldiiD, Ian Geoffrey MillsiD, Alessandro ProvenzaniiD
Abstract
Nicotinamide phosphoribosyltransferase (NAMPT) is the rate-limiting enzyme in the NAD+ salvage pathway and a promising therapeutic target in cancer. Resistance to NAMPT inhibitors, such as FK866, remains a key limitation to their clinical translation. While acquired resistance in cancer cell lines has been linked to target mutations, increased drug efflux and metabolic reprogramming, innate resistance mechanisms have been poorly studied. Addressing this gap is essential for identifying patient subgroups most likely to benefit from NAMPT-targeted therapies. Advanced castration resistance prostate cancer (CRPC) lacks effective targeted treatments. Among its heterogeneous subtypes, stem cell-like CRPC (CRPC-SCL) is defined by androgen receptor (AR) independence, YAP/TAZ dependency, and mesenchymal traits. In this study, we identify the YAP/nicotinamide N-methyltransferase (NNMT) axis as a key mediator of innate sensitivity to FK866 in stem-like mesenchymal CRPC cells. Using genetic and pharmacological models, we show that YAP or NNMT silencing rescues mesenchymal CRPC cells from FK866-induced apoptosis, endoplasmic reticulum stress, and NAD(H) loss. Metabolomic profiling confirmed that NNMT activity depletes nicotinamide, sensitizing cells to FK866. We further validated NNMT upregulation across clinical CRPC- SCL datasets, where it strongly correlates with mesenchymal and therapy-resistant phenotypes, as well as in murine prostate cancer cells with mesenchymal/stemness phenotypes. In conclusion, we identify the YAP/NNMT axis as a determinant of innate sensitivity to NAMPT inhibition in prostate cancer. These findings support the use of NNMT as a predictive biomarker for NAD+-targeting therapies and provide mechanistic insight into a metabolic vulnerability of the CRPC-SCL subtype. Targeting the YAP/NNMT/NAMPT axis may represent a novel strategy for treating stem-like/mesenchymal, therapy-resistant prostate cancers. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=118 SRC="FIGDIR/small/651153v2_ufig1.gif" ALT="Figure 1"> View larger version (15K): org.highwire.dtl.DTLVardef@de4237org.highwire.dtl.DTLVardef@1cd577corg.highwire.dtl.DTLVardef@2aa97corg.highwire.dtl.DTLVardef@dd2ac0_HPS_FORMAT_FIGEXP M_FIG C_FIG
- Citations
- 3
- FWCI
- 14.13
- Field percentile
- top 2%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Integrating pharmacogenomics data-driven prediction with bulk and single-cell RNAseq to demonstrate the efficacy of an NAMPT inhibitor against aggressive, taxane-resistant, and stem-like cells in lethal prostate cancer
Suman Mazumder, Taraswi Mitra Ghosh, … Amit Mitra·bioRxiv·Jul 20, 2022
- Targeting Pre-existing Club-Like Cells in Prostate Cancer Potentiates Androgen Deprivation Therapy
Manon Baurès, Anne-Sophie Vieira Aleixo, … Vincent Goffin·EMBO Molecular MedicinePeer-reviewed·Feb 2, 2026
- Iron Metabolism as a Therapeutic Vulnerability in Stem Cell-Like Castration-Resistant Prostate Cancer
Wanli Cheng, Andrea Brunello, … Marianna Kruithof‐de Julio·bioRxiv·Feb 25, 2026
- Dual inhibition of p38α MAPK and Casein kinase δ/ϵ as a novel treatment strategy for AR-independent and taxane-resistant advanced prostate cancer
Sayak Chakravarti, Suman Mazumder, … Amit Mitra·bioRxiv·Sep 30, 2026
- Understanding the development of enzalutamide resistance based on a functional single-cell approach
Changhui Xue, Hyun‐Kyung Ko, … David Z. Qian·The ProstatePeer-reviewed·Apr 10, 2025
- A synthetic lethal screen for Snail-induced enzalutamide resistance identifies JAK/STAT signaling as a therapeutic vulnerability in prostate cancer
K. E. Ware, B. C. Thomas, … J. A. Somarelli·Frontiers in Molecular BiosciencesPeer-reviewed·May 9, 2023