TY - JOUR
T1 - AR coactivators, CBP/p300, are critical mediators of DNA repair in prostate cancer
AU - Sardar, Sumaira
AU - McNair, Christopher M.
AU - Ravindranath, Lakshmi
AU - Chand, Saswati N.
AU - Yuan, Wei
AU - Bogdan, Denisa
AU - Welti, Jon
AU - Sharp, Adam
AU - Ryan, Natalie K.
AU - Knudsen, Liam A.
AU - Schiewer, Matthew J.
AU - DeArment, Elise G.
AU - Janas, Thomas
AU - Su, Xiaofeng A.
AU - Butler, Lisa M.
AU - de Bono, Johann S.
AU - Frese, Kris
AU - Brooks, Nigel
AU - Pegg, Neil
AU - Knudsen, Karen E.
AU - Shafi, Ayesha A.
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024
Y1 - 2024
N2 - Castration resistant prostate cancer (CRPC) remains an incurable disease stage with ineffective treatments options. Here, the androgen receptor (AR) coactivators CBP/p300, which are histone acetyltransferases, were identified as critical mediators of DNA damage repair (DDR) to potentially enhance therapeutic targeting of CRPC. Key findings demonstrate that CBP/p300 expression increases with disease progression and selects for poor prognosis in metastatic disease. CBP/p300 bromodomain inhibition enhances response to standard of care therapeutics. Functional studies, CBP/p300 cistrome mapping, and transcriptome in CRPC revealed that CBP/p300 regulates DDR. Further mechanistic investigation showed that CBP/p300 attenuation via therapeutic targeting and genomic knockdown decreases homologous recombination (HR) factors in vitro, in vivo, and in human prostate cancer (PCa) tumors ex vivo. Similarly, CBP/p300 expression in human prostate tissue correlates with HR factors. Lastly, targeting CBP/p300 impacts HR-mediate repair and patient outcome. Collectively, these studies identify CBP/p300 as drivers of PCa tumorigenesis and lay the groundwork to optimize therapeutic strategies for advanced PCa via CBP/p300 inhibition, potentially in combination with AR-directed and DDR therapies.
AB - Castration resistant prostate cancer (CRPC) remains an incurable disease stage with ineffective treatments options. Here, the androgen receptor (AR) coactivators CBP/p300, which are histone acetyltransferases, were identified as critical mediators of DNA damage repair (DDR) to potentially enhance therapeutic targeting of CRPC. Key findings demonstrate that CBP/p300 expression increases with disease progression and selects for poor prognosis in metastatic disease. CBP/p300 bromodomain inhibition enhances response to standard of care therapeutics. Functional studies, CBP/p300 cistrome mapping, and transcriptome in CRPC revealed that CBP/p300 regulates DDR. Further mechanistic investigation showed that CBP/p300 attenuation via therapeutic targeting and genomic knockdown decreases homologous recombination (HR) factors in vitro, in vivo, and in human prostate cancer (PCa) tumors ex vivo. Similarly, CBP/p300 expression in human prostate tissue correlates with HR factors. Lastly, targeting CBP/p300 impacts HR-mediate repair and patient outcome. Collectively, these studies identify CBP/p300 as drivers of PCa tumorigenesis and lay the groundwork to optimize therapeutic strategies for advanced PCa via CBP/p300 inhibition, potentially in combination with AR-directed and DDR therapies.
UR - http://www.scopus.com/inward/record.url?scp=85203713950&partnerID=8YFLogxK
U2 - 10.1038/s41388-024-03148-4
DO - 10.1038/s41388-024-03148-4
M3 - Article
AN - SCOPUS:85203713950
SN - 0950-9232
JO - Oncogene
JF - Oncogene
ER -