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Prostate Organoid Cultures as Tools to Translate Genotypes and Mutational Profiles to Pharmacological Responses
Published on: October 24, 2019
Comparative Proteomic and Transcriptomic Analysis of the Impact of Androgen Stimulation and Darolutamide Inhibition
Ekaterina Nevedomskaya1, Tatsuo Sugawara1, Simon J Baumgart1
1Bayer AG, Pharmaceuticals, Research & Early Development Oncology, 13353 Berlin, Germany.
Abstract:
Several inhibitors of androgen receptor (AR) function are approved for prostate cancer treatment, and their impact on gene transcription has been described. However, the ensuing effects at the protein level are far less well understood. We focused on the AR signaling inhibitor darolutamide and confirmed its strong AR binding and antagonistic activity using the high throughput cellular thermal shift assay (CETSA HT). Then, we generated comprehensive, quantitative proteomic data from the androgen-sensitive prostate cancer cell line VCaP and compared them to transcriptomic data. Following treatment with the synthetic androgen R1881 and darolutamide, global mass spectrometry-based proteomics and label-free quantification were performed. We found a generally good agreement between proteomic and transcriptomic data upon androgen stimulation and darolutamide inhibition. Similar effects were found both for the detected expressed genes and their protein products as well as for the corresponding biological programs. However, in a few instances there was a discrepancy in the magnitude of changes induced on gene expression levels compared to the corresponding protein levels, indicating post-transcriptional regulation of protein abundance. Chromatin immunoprecipitation DNA sequencing (ChIP-seq) and Hi-C chromatin immunoprecipitation (HiChIP) revealed the presence of androgen-activated AR-binding regions and long-distance AR-mediated loops at these genes.
Insights
Darolutamide effectively inhibits prostate cancer growth by blocking androgen receptor (AR) signaling. This study links gene changes to protein effects, revealing post-transcriptional regulation.
Area of Science:
- Oncology
- Molecular Biology
- Proteomics
Background:
- Androgen receptor (AR) inhibitors are crucial for prostate cancer treatment.
- Understanding AR inhibitor effects at the protein level is limited.
Purpose of the Study:
- To investigate the protein-level impact of the AR inhibitor darolutamide in prostate cancer cells.
- To compare proteomic and transcriptomic changes induced by darolutamide.
Main Methods:
- High throughput cellular thermal shift assay (CETSA HT) for AR binding.
- Quantitative mass spectrometry-based proteomics and label-free quantification.
- Chromatin immunoprecipitation DNA sequencing (ChIP-seq) and HiChIP.
Main Results:
- Darolutamide demonstrated strong AR binding and antagonistic activity.
- Proteomic and transcriptomic data showed good agreement upon androgen stimulation and inhibition.
- Discrepancies in gene vs. protein level changes indicated post-transcriptional regulation.
- AR-binding regions and long-distance AR-mediated loops were identified.
Conclusions:
- Darolutamide effectively inhibits AR signaling at both gene and protein levels.
- Post-transcriptional regulation plays a role in modulating protein abundance.
- AR-mediated chromatin looping influences gene regulation in response to androgens.

