The Projects of this Program have research strategies that variously involve genome-wide analysis of cancer cell epigenomes and transcriptomes and the use of screens involving genome editing. The primary objective of the Functional Epigenetics Core is to support the PO1 Projects with expertise in epigenetics approaches and CRISPR screens.
The specific aims of the Functional Epigenetics Core achieve this by providing the Program with the experimental and computational capabilities required to meet these essential programmatic needs. The Core is directed by Dr. Henry W. Long, an experienced, highly productive laboratory scientist based at the Center for Functional Cancer Epigenetics at the Dana Farber Cancer Institute in Boston. Dr. Long has a history of innovation in providing the critical resources and services to research projects in prostate and other cancers over the past 5 years at the CFCE. The Core is co-led by Dr. X Shirley Liu, a highly cited and productive computational biologist and biostatistician also based at the Dana Farber Cancer Institute. Dr. Liu has a very strong track record of innovation in epigenetics and CRISPR screening.
The Aims are 1) Support CRISPR screening approaches; 2) Provide capabilities and resources for performing complex epigenetic experiments; 3) Analysis and integration of epigenetic datasets; 4) Data sharing and management.
The primary objective of the Functional Epigenetics Core is to support the PO1 Projects with expertise in epigenetics approaches and CRISPR screens. The specific aims of the Functional Epigenetics Core achieve this by providing the Program with the experimental and computational capabilities required to meet these essential programmatic needs. The Core is directed by Dr. Henry W. Long, a highly productive laboratory scientist, and by Dr. X Shirley Liu, a renowned computational biologist and biostatistician with a track record of innovation in epigenetics and CRISPR screening.
|Beshiri, Michael L; Tice, Caitlin M; Tran, Crystal et al. (2018) A PDX/Organoid Biobank of Advanced Prostate Cancers Captures Genomic and Phenotypic Heterogeneity for Disease Modeling and Therapeutic Screening. Clin Cancer Res 24:4332-4345|
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|Mostaghel, Elahe A (2018) Alternative Acts: Oncogenic Splicing of Steroidogenic Enzymes in Prostate Cancer. Clin Cancer Res :|
|Uo, Takuma; Plymate, Stephen R; Sprenger, Cynthia C (2018) The potential of AR-V7 as a therapeutic target. Expert Opin Ther Targets 22:201-216|
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|Russo, Joshua W; Gao, Ce; Bhasin, Swati S et al. (2018) Downregulation of Dipeptidyl Peptidase 4 Accelerates Progression to Castration-Resistant Prostate Cancer. Cancer Res 78:6354-6362|
|Sowalsky, Adam G; Ye, Huihui; Bhasin, Manoj et al. (2018) Neoadjuvant-Intensive Androgen Deprivation Therapy Selects for Prostate Tumor Foci with Diverse Subclonal Oncogenic Alterations. Cancer Res 78:4716-4730|
|Zhu, Yezi; Sharp, Adam; Anderson, Courtney M et al. (2018) Novel Junction-specific and Quantifiable In Situ Detection of AR-V7 and its Clinical Correlates in Metastatic Castration-resistant Prostate Cancer. Eur Urol 73:727-735|
|Penning, Trevor M (2018) Dehydroepiandrosterone (DHEA)-SO4 Depot and Castration-Resistant Prostate Cancer. Vitam Horm 108:309-331|
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