Unravelling transcriptomic complexity in breast cancer through modulation of DARPP-32 expression and signalling pathways

• Published in: Scientific reports Vol. 13; no. 1; p. 21163
• Main Authors: Saidy, Behnaz, Vasan, Richa, Durant, Rosie, Greener, Megan-Rose, Immanuel, Adelynn, Green, Andrew R., Rakha, Emad, Ellis, Ian, Ball, Graham, Martin, Stewart G., Storr, Sarah J.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 30.11.2023; Nature Publishing Group; Nature Portfolio
• Subjects: 17β-Estradiol; 631/67/1347; 631/67/1857; Breast cancer; Breast Neoplasms - metabolism; Cell Adhesion Molecules - metabolism; DARPP-32 protein; Dkk1 protein; Dopamine and cAMP-Regulated Phosphoprotein 32 - metabolism; Female; Humanities and Social Sciences; Humans; Kallikreins; Kinases; Medical prognosis; Molecular modelling; multidisciplinary; Neural networks; Phosphorylation; Prognosis; Protein kinase A; Proteins; Receptor Protein-Tyrosine Kinases - metabolism; Science; Science (multidisciplinary); Signal Transduction; Threonine; Transcriptome; Transcriptomes; Transcriptomics
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-023-48198-y

DARPP-32 is a key regulator of protein-phosphatase-1 (PP-1) and protein kinase A (PKA), with its function dependent upon its phosphorylation state. We previously identified DKK1 and GRB7 as genes with linked expression using Artificial Neural Network (ANN) analysis; here, we determine protein expression in a large cohort of early-stage breast cancer patients. Low levels of DARPP-32 Threonine-34 phosphorylation and DKK1 expression were significantly associated with poor patient prognosis, while low levels of GRB7 expression were linked to better survival outcomes. To gain insight into mechanisms underlying these associations, we analysed the transcriptome of T47D breast cancer cells following DARPP-32 knockdown. We identified 202 differentially expressed transcripts and observed that some overlapped with genes implicated in the ANN analysis, including PTK7 , TRAF5 , and KLK6 , amongst others. Furthermore, we found that treatment of DARPP-32 knockdown cells with 17β-estradiol or PKA inhibitor fragment (6–22) amide led to the differential expression of 193 and 181 transcripts respectively. These results underscore the importance of DARPP-32, a central molecular switch, and its downstream targets, DKK1 and GRB7 in breast cancer. The discovery of common genes identified by a combined patient/cell line transcriptomic approach provides insights into the molecular mechanisms underlying differential breast cancer prognosis and highlights potential targets for therapeutic intervention.