Abstract B011: Iron Metabolism as a Therapeutic Vulnerability in Stem Cell-Like Castration-Resistant Prostate Cancer

Abstract Prostate cancer is the second most common malignancy among men, with androgen deprivation therapy (ADT) serving as the standard treatment due to the hormone sensitivity of prostate tumors. However, therapeutic resistance frequently develops, leading to castration-resistant prostate cancer (CRPC), an aggressive and lethal disease. A recently defined subtype, stem cell-like CRPC (CRPC-SCL), accounts for approximately 25% of CRPC cases and demonstrates poor responsiveness to ADT. CRPC-SCL is characterized by the expression of CD44, a glycoprotein that promotes hyaluronic acid binding and uptake. Single-cell RNA sequencing (scRNA-seq) analysis of CRPC patient samples revealed that CD44hi cells are predominantly enriched within a specific cluster and exhibit distinct stem cell-like characteristics. Functionally, in a CRPC-SCL patient-derived xenograft (PDX) model, the CD44hi subpopulation demonstrated enhanced tumorigenic and proliferative capacities, indicating that these cells represent a more aggressive and malignant fraction within the CRPC-SCL tumor. Mechanistically, iron metabolism emerged as a critical regulator of CD44hi cell function. These cells maintain elevated intracellular iron levels, which can translocate into the nucleus to activate the H3K9me2 demethylase KDM3A. Activation of KDM3A sustains CD44 expression and reinforces stem cell-like properties through modulation of H3K9me2 histone modification. Exploiting this metabolic vulnerability, inhibition of the iron-regulatory factor NRF2 was found to decrease ferritin expression and increase intracellular free iron. The resultant iron overload selectively induces ferroptosis in CD44hi cells. Collectively, these findings reveal that targeting iron metabolism to trigger ferroptotic cell death represents a promising therapeutic strategy for the treatment of CRPC-SCL. Citation Format: Wanli Cheng, Andrea Brunello, Panagiotis Chouvardas, Sofia Karkampouna, Marianna Kruithof-de. Julio. Iron Metabolism as a Therapeutic Vulnerability in Stem Cell-Like Castration-Resistant Prostate Cancer [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Innovations in Prostate Cancer Research and Treatment; 2026 Jan 20-22; Philadelphia PA. Philadelphia (PA): AACR; Cancer Res 2026;86(2_Suppl):Abstract nr B011.

Authors

Institutions

Publication Details

Journal
Cancer Research
Published
2026-01-20
DOI
https://doi.org/10.1158/1538-7445.prostateca26-b011
Primary Topic
Ferroptosis and cancer prognosis
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract B011: Iron Metabolism as a Therapeutic Vulnerability in Stem Cell-Like Castration-Resistant Prostate Cancer

Panagiotis Chouvardas, Sofia Karkampouna, Marianna Kruithof-de Julio, Wanli Cheng et al.
Cancer Research
Ferroptosis and cancer prognosis
article

Abstract B011: Iron Metabolism as a Therapeutic Vulnerability in Stem Cell-Like Castration-Resistant Prostate Cancer

Panagiotis Chouvardas, Sofia Karkampouna, Marianna Kruithof-de Julio, Wanli Cheng, Andrea Brunello
article en

Abstract

Abstract Prostate cancer is the second most common malignancy among men, with androgen deprivation therapy (ADT) serving as the standard treatment due to the hormone sensitivity of prostate tumors. However, therapeutic resistance frequently develops, leading to castration-resistant prostate cancer (CRPC), an aggressive and lethal disease. A recently defined subtype, stem cell-like CRPC (CRPC-SCL), accounts for approximately 25% of CRPC cases and demonstrates poor responsiveness to ADT. CRPC-SCL is characterized by the expression of CD44, a glycoprotein that promotes hyaluronic acid binding and uptake. Single-cell RNA sequencing (scRNA-seq) analysis of CRPC patient samples revealed that CD44hi cells are predominantly enriched within a specific cluster and exhibit distinct stem cell-like characteristics. Functionally, in a CRPC-SCL patient-derived xenograft (PDX) model, the CD44hi subpopulation demonstrated enhanced tumorigenic and proliferative capacities, indicating that these cells represent a more aggressive and malignant fraction within the CRPC-SCL tumor. Mechanistically, iron metabolism emerged as a critical regulator of CD44hi cell function. These cells maintain elevated intracellular iron levels, which can translocate into the nucleus to activate the H3K9me2 demethylase KDM3A. Activation of KDM3A sustains CD44 expression and reinforces stem cell-like properties through modulation of H3K9me2 histone modification. Exploiting this metabolic vulnerability, inhibition of the iron-regulatory factor NRF2 was found to decrease ferritin expression and increase intracellular free iron. The resultant iron overload selectively induces ferroptosis in CD44hi cells. Collectively, these findings reveal that targeting iron metabolism to trigger ferroptotic cell death represents a promising therapeutic strategy for the treatment of CRPC-SCL. Citation Format: Wanli Cheng, Andrea Brunello, Panagiotis Chouvardas, Sofia Karkampouna, Marianna Kruithof-de. Julio. Iron Metabolism as a Therapeutic Vulnerability in Stem Cell-Like Castration-Resistant Prostate Cancer [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Innovations in Prostate Cancer Research and Treatment; 2026 Jan 20-22; Philadelphia PA. Philadelphia (PA): AACR; Cancer Res 2026;86(2_Suppl):Abstract nr B011.

Cancer ResearchVol. 86(2_Supplement)
University of Bern (CH), Bern University of Applied Sciences (CH)
No poverty
Openalex Percentile: Top 83%
Ferroptosis and cancer prognosis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.