Abstract 2998: Disrupted clock pathway during lineage plasticity and prostate cancer progression

Abstract Most treatment resistant prostate cancers are driven by androgen receptor (AR) signaling. However, AR-negative prostate cancer has been increasingly recognized as the mechanism of resistance, particularly as potent AR-targeted therapies have been introduced earlier in the treatment paradigm. Lineage plasticity and histologic transformation of AR-driven prostate adenocarcinoma to AR-negative neuroendocrine prostate cancer (NEPC) represents one of the most lethal forms of prostate cancer. Here, we explored how the circadian clock pathway changes occur during lineage plasticity and prostate cancer progression. We identified loss of rhythmicity in the expression of clock regulated genes. Clock pathway regulators RORα, BMAL1, and CLOCK are highly expressed in NEPC compared to prostate adenocarcinoma. RORA displays marked upregulation in prostate tumors after AR targeted therapy relative to matched pre-therapy tumors. RORA overexpression in prostate adenocarcinoma models led to increased cell proliferation and enriched cell cycle pathway. Importantly, we noted that clock pathway is reprogrammed differently in AR-dependent and AR-independent prostate tumors. For instance, RORA overexpression in AR-dependent adenocarcinoma cells resulted in enriched androgen response and enhanced sensitivity towards AR-targeted pathway inhibitors. RORA knockout in AR-independent models resulted in increased expression of mitochondrial genes and increased sensitivity towards oxidative phosphorylation (OXPHOS) inhibitors. Moreover, targeting RORα in NEPC patient-derived organoids and mouse xenograft models abrogated tumor growth and downregulated the NEPC phenotype. Altogether, our findings point to a mechanistic regulation of clock genes including RORα during prostate cancer progression and nominates potential new strategies to target lineage plasticity. Citation Format: Nishat Manzar, Himisha Beltran. Disrupted clock pathway during lineage plasticity and prostate cancer progression [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2998.

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Publication Details

Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-2998
Primary Topic
Circadian rhythm and melatonin
Type
article
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article

Abstract 2998: Disrupted clock pathway during lineage plasticity and prostate cancer progression

Himisha Beltran, Nishat Manzar
Cancer Research
Circadian rhythm and melatonin
article

Abstract 2998: Disrupted clock pathway during lineage plasticity and prostate cancer progression

Himisha Beltran, Nishat Manzar
article en

Abstract

Abstract Most treatment resistant prostate cancers are driven by androgen receptor (AR) signaling. However, AR-negative prostate cancer has been increasingly recognized as the mechanism of resistance, particularly as potent AR-targeted therapies have been introduced earlier in the treatment paradigm. Lineage plasticity and histologic transformation of AR-driven prostate adenocarcinoma to AR-negative neuroendocrine prostate cancer (NEPC) represents one of the most lethal forms of prostate cancer. Here, we explored how the circadian clock pathway changes occur during lineage plasticity and prostate cancer progression. We identified loss of rhythmicity in the expression of clock regulated genes. Clock pathway regulators RORα, BMAL1, and CLOCK are highly expressed in NEPC compared to prostate adenocarcinoma. RORA displays marked upregulation in prostate tumors after AR targeted therapy relative to matched pre-therapy tumors. RORA overexpression in prostate adenocarcinoma models led to increased cell proliferation and enriched cell cycle pathway. Importantly, we noted that clock pathway is reprogrammed differently in AR-dependent and AR-independent prostate tumors. For instance, RORA overexpression in AR-dependent adenocarcinoma cells resulted in enriched androgen response and enhanced sensitivity towards AR-targeted pathway inhibitors. RORA knockout in AR-independent models resulted in increased expression of mitochondrial genes and increased sensitivity towards oxidative phosphorylation (OXPHOS) inhibitors. Moreover, targeting RORα in NEPC patient-derived organoids and mouse xenograft models abrogated tumor growth and downregulated the NEPC phenotype. Altogether, our findings point to a mechanistic regulation of clock genes including RORα during prostate cancer progression and nominates potential new strategies to target lineage plasticity. Citation Format: Nishat Manzar, Himisha Beltran. Disrupted clock pathway during lineage plasticity and prostate cancer progression [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2998.

Cancer ResearchVol. 86(7_Supplement)
Harvard University (US), Dana-Farber Cancer Institute (US)
Good health and well-being
Openalex Percentile: Top 7%
Circadian rhythm and melatonin
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