Abstract PR032: Therapeutic targeting of eIF4E cap-binding domain reveals control of lineage fate in prostate cancer

Abstract A hallmark of therapy resistance in advanced castration-resistant prostate cancer (CRPC) is the transition between lineage states from androgen receptor (AR)-dependent to AR-independent phenotypes. Elucidating the mechanisms underlying this lineage plasticity is crucial, as these transitions may represent druggable processes that could be leveraged to resensitize prostate cancer to AR pathway inhibitors (ARPIs) or prevent resistance altogether. Here, we investigated how mRNA translation regulates lineage plasticity and contributes to therapy resistance in prostate cancer. Using nascent proteome mass spectrometry (HPG-TMT), we demonstrate that basal-to-luminal lineage plasticity in prostate epithelium is regulated by the eIF4E cap-binding domain. Mechanistically, inhibition of this domain represses translational of basal keratins via cis-regulatory elements in the 5' untranslated regions (UTRs) of their transcripts, while enhancing AR protein stability through the translational upregulation of the deubiquitinases BAP1 and OTUD3.This coordinated translational reprogramming drives a basal-to-luminal lineage switch essential for cell survival and represents a druggable vulnerability. Clinically, elevated eIF4E expression in CRPC is associated with basal phenotype, reduced luminal differentiation and accelerated resistance to ARPIs. Notably, tumors resistant to enzalutamide regain sensitivity upon inhibition of the eIF4E cap-binding domain, which reprograms them toward a luminal state. These findings identify a novel oncogenic role of the eIF4E cap-binding domain in regulating lineage plasticity and therapy resistance, highlighting its inhibition as a promising strategy to overcome treatment resistance in CRPC. Citation Format: Rashmi Mishra, Sihyeon Song, Dhruv Choradia, Dmytro Rudoy, Cindy L. Wladyka, Patrick Hoang, Jin Yeong kim, Ilsa Coleman, Sonali Arora, Alexander Orellana, ChenWei Lin, Philip Gafken, Eva Corey, Peter Nelson, Haolong Li, Arnab Sengupta, Andrew C. Hsieh. Therapeutic targeting of eIF4E cap-binding domain reveals control of lineage fate in 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 PR032.

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Journal
Cancer Research
Published
2026-01-20
DOI
https://doi.org/10.1158/1538-7445.prostateca26-pr032
Primary Topic
PI3K/AKT/mTOR signaling in cancer
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article
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article

Abstract PR032: Therapeutic targeting of eIF4E cap-binding domain reveals control of lineage fate in prostate cancer

Andrew Caleb Hsieh, Dmytro Rudoy, I Coleman, Rashmi Mishra et al.
Cancer Research
PI3K/AKT/mTOR signaling in cancer
article

Abstract PR032: Therapeutic targeting of eIF4E cap-binding domain reveals control of lineage fate in prostate cancer

Andrew Caleb Hsieh, Dmytro Rudoy, I Coleman, Rashmi Mishra, Philip R. Gafken, Patrick Hoang, Arnab Sengupta, Haolong Li, Cindy L. Wladyka, Sonali Arora, Jin Yeong kim, Eva Corey, Dhruv Choradia, Peter Nelson, ChenWei Lin, Alexander Orellana, Sihyeon Song
article en

Abstract

Abstract A hallmark of therapy resistance in advanced castration-resistant prostate cancer (CRPC) is the transition between lineage states from androgen receptor (AR)-dependent to AR-independent phenotypes. Elucidating the mechanisms underlying this lineage plasticity is crucial, as these transitions may represent druggable processes that could be leveraged to resensitize prostate cancer to AR pathway inhibitors (ARPIs) or prevent resistance altogether. Here, we investigated how mRNA translation regulates lineage plasticity and contributes to therapy resistance in prostate cancer. Using nascent proteome mass spectrometry (HPG-TMT), we demonstrate that basal-to-luminal lineage plasticity in prostate epithelium is regulated by the eIF4E cap-binding domain. Mechanistically, inhibition of this domain represses translational of basal keratins via cis-regulatory elements in the 5' untranslated regions (UTRs) of their transcripts, while enhancing AR protein stability through the translational upregulation of the deubiquitinases BAP1 and OTUD3.This coordinated translational reprogramming drives a basal-to-luminal lineage switch essential for cell survival and represents a druggable vulnerability. Clinically, elevated eIF4E expression in CRPC is associated with basal phenotype, reduced luminal differentiation and accelerated resistance to ARPIs. Notably, tumors resistant to enzalutamide regain sensitivity upon inhibition of the eIF4E cap-binding domain, which reprograms them toward a luminal state. These findings identify a novel oncogenic role of the eIF4E cap-binding domain in regulating lineage plasticity and therapy resistance, highlighting its inhibition as a promising strategy to overcome treatment resistance in CRPC. Citation Format: Rashmi Mishra, Sihyeon Song, Dhruv Choradia, Dmytro Rudoy, Cindy L. Wladyka, Patrick Hoang, Jin Yeong kim, Ilsa Coleman, Sonali Arora, Alexander Orellana, ChenWei Lin, Philip Gafken, Eva Corey, Peter Nelson, Haolong Li, Arnab Sengupta, Andrew C. Hsieh. Therapeutic targeting of eIF4E cap-binding domain reveals control of lineage fate in 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 PR032.

Cancer ResearchVol. 86(2_Supplement)
Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa (ZA), Georgia College & State University (US), University of Washington (US), Fred Hutch Cancer Center (US)
Good health and well-being
Openalex Percentile: Top 84%
PI3K/AKT/mTOR signaling in cancer
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