Metabolic and imaging phenotypes associated with RB1 loss in castrate resistant prostate cancer

Motivation: The progression of prostate cancer is marked by both RB1 and T53 inactivation and higher 18FDG-PET uptake, but it's unclear whether RB1 or TP53 inactivation drives increased glucose import. Goal(s): Can metabolic changes be used as a biomarker for RB1 and TP53 loss?Approach: Metabolomic analysis by NMR and IC-MS for a comprehensive measure of metabolic changes ex vivo and and hyperpolarized MRI to measure the Warburg effect in vivo. Results: 18FDG uptake was unaffected by loss of either RB1 or TP53. RB1 and TP53 did induce a series of other metabolic changes which could be detected in vivo by hyperpolarized MRIImpact: Neuroendrocrine prostate cancer is a life-threatening progression of prostate cancer that is characterized by mutations in two key genes. Hyperpolarized MRI may enhance early diagnosis of NEPC without biopsy.

Authors

Publication Details

Journal
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Published
2024-11-26
DOI
https://doi.org/10.58530/2024/0702
Primary Topic
Prostate Cancer Treatment and Research
Type
article
Field-Weighted Citation Impact
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article

Metabolic and imaging phenotypes associated with RB1 loss in castrate resistant prostate cancer

Murali Cherukuri, Margaret White, Aian Alilin, Jeffrey Brender et al.
1 links
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Prostate Cancer Treatment and Research
article

Metabolic and imaging phenotypes associated with RB1 loss in castrate resistant prostate cancer

Murali Cherukuri, Margaret White, Aian Alilin, Jeffrey Brender, Ye Yang, Fahim Ahmad, Jürgen Seidel, Sonam Raj, Kazutoshi Yamamoto, Colleen P. Olkowski, Brian J. Capaldo, Stephen Adler, Peter L. Choyke, Supreet Agarwal, Kathleen Kelly, Daniel R. Crooks, Anita Ton
article en

Abstract

Motivation: The progression of prostate cancer is marked by both RB1 and T53 inactivation and higher 18FDG-PET uptake, but it's unclear whether RB1 or TP53 inactivation drives increased glucose import. Goal(s): Can metabolic changes be used as a biomarker for RB1 and TP53 loss?Approach: Metabolomic analysis by NMR and IC-MS for a comprehensive measure of metabolic changes ex vivo and and hyperpolarized MRI to measure the Warburg effect in vivo. Results: 18FDG uptake was unaffected by loss of either RB1 or TP53. RB1 and TP53 did induce a series of other metabolic changes which could be detected in vivo by hyperpolarized MRIImpact: Neuroendrocrine prostate cancer is a life-threatening progression of prostate cancer that is characterized by mutations in two key genes. Hyperpolarized MRI may enhance early diagnosis of NEPC without biopsy.

Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Openalex Percentile: Top 60%
Prostate Cancer Treatment and Research
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