Ontology highlight
ABSTRACT: Background
After long-term androgen deprivation therapy, 25-30% prostate cancer (PCa) acquires an aggressive neuroendocrine (NE) phenotype. Dysregulation of YAP1, a key transcription coactivator of the Hippo pathway, has been related to cancer progression. However, its role in neuroendocrine prostate cancer (NEPC) has not been assessed.Methods
Immunohistochemistry and bioinformatics analysis were conducted to evaluate YAP1 expression levels during PCa initiation and progression.Results
YAP1 expression was present in the basal epithelial cells in benign prostatic tissues, lost in low-grade PCa, but elevated in high-grade prostate adenocarcinomas. Interestingly, the expression of YAP1 was reduced/lost in both human and mouse NEPC.Conclusions
The expression of YAP1 is elevated in high-grade prostate adenocarcinomas but lost in NEPC.
SUBMITTER: Cheng S
PROVIDER: S-EPMC7572469 | biostudies-literature | 2020 Dec
REPOSITORIES: biostudies-literature
Cheng Siyuan S Prieto-Dominguez Nestor N Yang Shu S Connelly Zachary M ZM StPierre Samantha S Rushing Bryce B Watkins Andy A Shi Lawrence L Lakey Meredith M Baiamonte Lyndsey Buckner LB Fazili Tajammul T Lurie Aubrey A Corey Eva E Shi Runhua R Yeh Yunshin Y Yu Xiuping X
Prostate cancer and prostatic diseases 20200420 4
<h4>Background</h4>After long-term androgen deprivation therapy, 25-30% prostate cancer (PCa) acquires an aggressive neuroendocrine (NE) phenotype. Dysregulation of YAP1, a key transcription coactivator of the Hippo pathway, has been related to cancer progression. However, its role in neuroendocrine prostate cancer (NEPC) has not been assessed.<h4>Methods</h4>Immunohistochemistry and bioinformatics analysis were conducted to evaluate YAP1 expression levels during PCa initiation and progression.< ...[more]