Chromatin profiles classify castration-resistant prostate cancers suggesting therapeutic targets
Cornell University · Weill Cornell Medicine · +6 more institutions
Abstract
In castration-resistant prostate cancer (CRPC), the loss of androgen receptor (AR) dependence leads to clinically aggressive tumors with few therapeutic options. We used ATAC-seq (assay for transposase-accessible chromatin sequencing), RNA-seq, and DNA sequencing to investigate 22 organoids, six patient-derived xenografts, and 12 cell lines. We identified the well-characterized AR-dependent and neuroendocrine subtypes, as well as two AR-negative/low groups: a Wnt-dependent subtype, and a stem cell-like (SCL) subtype driven by activator protein-1 (AP-1) transcription factors. We used transcriptomic signatures to classify 366 patients, which showed that SCL is the second most common subtype of CRPC after…
Citation impact
- FWCI
- 36.56
- Percentile
- 100%
- References
- 82
Authors
32- FTFanying TangCorresponding
Cornell University, Weill Cornell Medicine
- DXDuo XuCorresponding
Cornell University, Weill Cornell Medicine
- SWShangqian WangCorresponding
Memorial Sloan Kettering Cancer Center, Nanjing Medical University
- CKChen Khuan WongCorresponding
Memorial Sloan Kettering Cancer Center
- AMAlexander Martinez‐Fundichely
Cornell University, Weill Cornell Medicine
Topics & keywords
- Chromatin
- Prostate cancer
- Transcriptome
- Androgen receptor
- Biology
- Cancer research
- Computational biology
- FOXA1
- Good health and well-being