SRX2880437 GSM2648116 SRP074150 SRS2248328 SAMN07189708 RNA-Seq TRANSCRIPTOMIC cDNA Frozen xenograft tumors were finely grinded using cold hammer and a pestle. The pestle was placed over dry ice to maintain it at low temperatures. The ground tumor was suspended in ice-cold PBS and dounce homogenized and subsequently washed twice with ice-cold PBS. The cell pellets obtained from and washed xenografts were processed similar to the pellets obtained from in-vitro experiments (RNA-seq protocol). Hormone-treated cells were homogenized and total RNA was extracted using Qiagen RNAeasy kit. PolyA tail selection was performed on 250 ng of total RNA. RNA-seq libraries were prepared using NEBNext kit. Details of library preparation strategy are provided in the materials and methods section (RNA expression and RNA-sequencing) of the paper. NextSeq 500 gds 302648116 GSM2648116 GEO Accession GSM2648116 SRX2880438 GSM2648117 SRP074150 SRS2248329 SAMN07189707 RNA-Seq TRANSCRIPTOMIC cDNA Frozen xenograft tumors were finely grinded using cold hammer and a pestle. The pestle was placed over dry ice to maintain it at low temperatures. The ground tumor was suspended in ice-cold PBS and dounce homogenized and subsequently washed twice with ice-cold PBS. The cell pellets obtained from and washed xenografts were processed similar to the pellets obtained from in-vitro experiments (RNA-seq protocol). Hormone-treated cells were homogenized and total RNA was extracted using Qiagen RNAeasy kit. PolyA tail selection was performed on 250 ng of total RNA. RNA-seq libraries were prepared using NEBNext kit. Details of library preparation strategy are provided in the materials and methods section (RNA expression and RNA-sequencing) of the paper. NextSeq 500 gds 302648117 GSM2648117 GEO Accession GSM2648117 SRX2880439 GSM2648118 SRP074150 SRS2248330 SAMN07189706 RNA-Seq TRANSCRIPTOMIC cDNA Frozen xenograft tumors were finely grinded using cold hammer and a pestle. The pestle was placed over dry ice to maintain it at low temperatures. The ground tumor was suspended in ice-cold PBS and dounce homogenized and subsequently washed twice with ice-cold PBS. The cell pellets obtained from and washed xenografts were processed similar to the pellets obtained from in-vitro experiments (RNA-seq protocol). Hormone-treated cells were homogenized and total RNA was extracted using Qiagen RNAeasy kit. PolyA tail selection was performed on 250 ng of total RNA. RNA-seq libraries were prepared using NEBNext kit. Details of library preparation strategy are provided in the materials and methods section (RNA expression and RNA-sequencing) of the paper. NextSeq 500 gds 302648118 GSM2648118 GEO Accession GSM2648118 SRX2880440 GSM2648119 SRP074150 SRS2248331 SAMN07189709 RNA-Seq TRANSCRIPTOMIC cDNA Frozen xenograft tumors were finely grinded using cold hammer and a pestle. The pestle was placed over dry ice to maintain it at low temperatures. The ground tumor was suspended in ice-cold PBS and dounce homogenized and subsequently washed twice with ice-cold PBS. The cell pellets obtained from and washed xenografts were processed similar to the pellets obtained from in-vitro experiments (RNA-seq protocol). Hormone-treated cells were homogenized and total RNA was extracted using Qiagen RNAeasy kit. PolyA tail selection was performed on 250 ng of total RNA. RNA-seq libraries were prepared using NEBNext kit. Details of library preparation strategy are provided in the materials and methods section (RNA expression and RNA-sequencing) of the paper. NextSeq 500 gds 302648119 GSM2648119 GEO Accession GSM2648119 SRX2880441 GSM2648120 SRP074150 SRS2248332 SAMN07189710 RNA-Seq TRANSCRIPTOMIC cDNA Frozen xenograft tumors were finely grinded using cold hammer and a pestle. The pestle was placed over dry ice to maintain it at low temperatures. The ground tumor was suspended in ice-cold PBS and dounce homogenized and subsequently washed twice with ice-cold PBS. The cell pellets obtained from and washed xenografts were processed similar to the pellets obtained from in-vitro experiments (RNA-seq protocol). Hormone-treated cells were homogenized and total RNA was extracted using Qiagen RNAeasy kit. PolyA tail selection was performed on 250 ng of total RNA. RNA-seq libraries were prepared using NEBNext kit. Details of library preparation strategy are provided in the materials and methods section (RNA expression and RNA-sequencing) of the paper. NextSeq 500 gds 302648120 GSM2648120 GEO Accession GSM2648120 SRX2880442 GSM2648121 SRP074150 SRS2248333 SAMN07189705 RNA-Seq TRANSCRIPTOMIC cDNA Frozen xenograft tumors were finely grinded using cold hammer and a pestle. The pestle was placed over dry ice to maintain it at low temperatures. The ground tumor was suspended in ice-cold PBS and dounce homogenized and subsequently washed twice with ice-cold PBS. The cell pellets obtained from and washed xenografts were processed similar to the pellets obtained from in-vitro experiments (RNA-seq protocol). Hormone-treated cells were homogenized and total RNA was extracted using Qiagen RNAeasy kit. PolyA tail selection was performed on 250 ng of total RNA. RNA-seq libraries were prepared using NEBNext kit. Details of library preparation strategy are provided in the materials and methods section (RNA expression and RNA-sequencing) of the paper. NextSeq 500 gds 302648121 GSM2648121 GEO Accession GSM2648121 SRX2880443 GSM2648122 SRP074150 SRS2248334 SAMN07189704 RNA-Seq TRANSCRIPTOMIC cDNA Frozen xenograft tumors were finely grinded using cold hammer and a pestle. The pestle was placed over dry ice to maintain it at low temperatures. The ground tumor was suspended in ice-cold PBS and dounce homogenized and subsequently washed twice with ice-cold PBS. The cell pellets obtained from and washed xenografts were processed similar to the pellets obtained from in-vitro experiments (RNA-seq protocol). Hormone-treated cells were homogenized and total RNA was extracted using Qiagen RNAeasy kit. PolyA tail selection was performed on 250 ng of total RNA. RNA-seq libraries were prepared using NEBNext kit. Details of library preparation strategy are provided in the materials and methods section (RNA expression and RNA-sequencing) of the paper. NextSeq 500 gds 302648122 GSM2648122 GEO Accession GSM2648122 SRX2880444 GSM2648123 SRP074150 SRS2248335 SAMN07189703 RNA-Seq TRANSCRIPTOMIC cDNA Frozen xenograft tumors were finely grinded using cold hammer and a pestle. The pestle was placed over dry ice to maintain it at low temperatures. The ground tumor was suspended in ice-cold PBS and dounce homogenized and subsequently washed twice with ice-cold PBS. The cell pellets obtained from and washed xenografts were processed similar to the pellets obtained from in-vitro experiments (RNA-seq protocol). Hormone-treated cells were homogenized and total RNA was extracted using Qiagen RNAeasy kit. PolyA tail selection was performed on 250 ng of total RNA. RNA-seq libraries were prepared using NEBNext kit. Details of library preparation strategy are provided in the materials and methods section (RNA expression and RNA-sequencing) of the paper. NextSeq 500 gds 302648123 GSM2648123 GEO Accession GSM2648123 SRX2880445 GSM2648124 SRP074150 SRS2248336 SAMN07189702 RNA-Seq TRANSCRIPTOMIC cDNA Frozen xenograft tumors were finely grinded using cold hammer and a pestle. The pestle was placed over dry ice to maintain it at low temperatures. The ground tumor was suspended in ice-cold PBS and dounce homogenized and subsequently washed twice with ice-cold PBS. The cell pellets obtained from and washed xenografts were processed similar to the pellets obtained from in-vitro experiments (RNA-seq protocol). Hormone-treated cells were homogenized and total RNA was extracted using Qiagen RNAeasy kit. PolyA tail selection was performed on 250 ng of total RNA. RNA-seq libraries were prepared using NEBNext kit. Details of library preparation strategy are provided in the materials and methods section (RNA expression and RNA-sequencing) of the paper. NextSeq 500 gds 302648124 GSM2648124 GEO Accession GSM2648124 SRX2880446 GSM2648125 SRP074150 SRS2248337 SAMN07189701 RNA-Seq TRANSCRIPTOMIC cDNA Frozen xenograft tumors were finely grinded using cold hammer and a pestle. The pestle was placed over dry ice to maintain it at low temperatures. The ground tumor was suspended in ice-cold PBS and dounce homogenized and subsequently washed twice with ice-cold PBS. The cell pellets obtained from and washed xenografts were processed similar to the pellets obtained from in-vitro experiments (RNA-seq protocol). Hormone-treated cells were homogenized and total RNA was extracted using Qiagen RNAeasy kit. PolyA tail selection was performed on 250 ng of total RNA. RNA-seq libraries were prepared using NEBNext kit. Details of library preparation strategy are provided in the materials and methods section (RNA expression and RNA-sequencing) of the paper. NextSeq 500 gds 302648125 GSM2648125 GEO Accession GSM2648125 SRX2880447 GSM2648126 SRP074150 SRS2248338 SAMN07189700 RNA-Seq TRANSCRIPTOMIC cDNA Frozen xenograft tumors were finely grinded using cold hammer and a pestle. The pestle was placed over dry ice to maintain it at low temperatures. The ground tumor was suspended in ice-cold PBS and dounce homogenized and subsequently washed twice with ice-cold PBS. The cell pellets obtained from and washed xenografts were processed similar to the pellets obtained from in-vitro experiments (RNA-seq protocol). Hormone-treated cells were homogenized and total RNA was extracted using Qiagen RNAeasy kit. PolyA tail selection was performed on 250 ng of total RNA. RNA-seq libraries were prepared using NEBNext kit. Details of library preparation strategy are provided in the materials and methods section (RNA expression and RNA-sequencing) of the paper. NextSeq 500 gds 302648126 GSM2648126 GEO Accession GSM2648126 SRX2880448 GSM2648127 SRP074150 SRS2248339 SAMN07189699 RNA-Seq TRANSCRIPTOMIC cDNA Frozen xenograft tumors were finely grinded using cold hammer and a pestle. The pestle was placed over dry ice to maintain it at low temperatures. The ground tumor was suspended in ice-cold PBS and dounce homogenized and subsequently washed twice with ice-cold PBS. The cell pellets obtained from and washed xenografts were processed similar to the pellets obtained from in-vitro experiments (RNA-seq protocol). Hormone-treated cells were homogenized and total RNA was extracted using Qiagen RNAeasy kit. PolyA tail selection was performed on 250 ng of total RNA. RNA-seq libraries were prepared using NEBNext kit. Details of library preparation strategy are provided in the materials and methods section (RNA expression and RNA-sequencing) of the paper. NextSeq 500 gds 302648127 GSM2648127 GEO Accession GSM2648127 SRX2880449 GSM2648128 SRP074150 SRS2248340 SAMN07189698 RNA-Seq TRANSCRIPTOMIC cDNA Frozen xenograft tumors were finely grinded using cold hammer and a pestle. The pestle was placed over dry ice to maintain it at low temperatures. The ground tumor was suspended in ice-cold PBS and dounce homogenized and subsequently washed twice with ice-cold PBS. The cell pellets obtained from and washed xenografts were processed similar to the pellets obtained from in-vitro experiments (RNA-seq protocol). Hormone-treated cells were homogenized and total RNA was extracted using Qiagen RNAeasy kit. PolyA tail selection was performed on 250 ng of total RNA. RNA-seq libraries were prepared using NEBNext kit. Details of library preparation strategy are provided in the materials and methods section (RNA expression and RNA-sequencing) of the paper. NextSeq 500 gds 302648128 GSM2648128 GEO Accession GSM2648128 SRX2880450 GSM2648129 SRP074150 SRS2248342 SAMN07189697 RNA-Seq TRANSCRIPTOMIC cDNA Frozen xenograft tumors were finely grinded using cold hammer and a pestle. The pestle was placed over dry ice to maintain it at low temperatures. The ground tumor was suspended in ice-cold PBS and dounce homogenized and subsequently washed twice with ice-cold PBS. The cell pellets obtained from and washed xenografts were processed similar to the pellets obtained from in-vitro experiments (RNA-seq protocol). Hormone-treated cells were homogenized and total RNA was extracted using Qiagen RNAeasy kit. PolyA tail selection was performed on 250 ng of total RNA. RNA-seq libraries were prepared using NEBNext kit. Details of library preparation strategy are provided in the materials and methods section (RNA expression and RNA-sequencing) of the paper. NextSeq 500 gds 302648129 GSM2648129 GEO Accession GSM2648129 SRX2880451 GSM2648130 SRP074150 SRS2248341 SAMN07189696 RNA-Seq TRANSCRIPTOMIC cDNA Frozen xenograft tumors were finely grinded using cold hammer and a pestle. The pestle was placed over dry ice to maintain it at low temperatures. The ground tumor was suspended in ice-cold PBS and dounce homogenized and subsequently washed twice with ice-cold PBS. The cell pellets obtained from and washed xenografts were processed similar to the pellets obtained from in-vitro experiments (RNA-seq protocol). Hormone-treated cells were homogenized and total RNA was extracted using Qiagen RNAeasy kit. PolyA tail selection was performed on 250 ng of total RNA. RNA-seq libraries were prepared using NEBNext kit. Details of library preparation strategy are provided in the materials and methods section (RNA expression and RNA-sequencing) of the paper. NextSeq 500 gds 302648130 GSM2648130 GEO Accession GSM2648130 SRX2880452 GSM2648131 SRP074150 SRS2248343 SAMN07189695 RNA-Seq TRANSCRIPTOMIC cDNA Frozen xenograft tumors were finely grinded using cold hammer and a pestle. The pestle was placed over dry ice to maintain it at low temperatures. The ground tumor was suspended in ice-cold PBS and dounce homogenized and subsequently washed twice with ice-cold PBS. The cell pellets obtained from and washed xenografts were processed similar to the pellets obtained from in-vitro experiments (RNA-seq protocol). Hormone-treated cells were homogenized and total RNA was extracted using Qiagen RNAeasy kit. PolyA tail selection was performed on 250 ng of total RNA. RNA-seq libraries were prepared using NEBNext kit. Details of library preparation strategy are provided in the materials and methods section (RNA expression and RNA-sequencing) of the paper. NextSeq 500 gds 302648131 GSM2648131 GEO Accession GSM2648131 SRX2880453 GSM2648132 SRP074150 SRS2248344 SAMN07189694 RNA-Seq TRANSCRIPTOMIC cDNA Frozen xenograft tumors were finely grinded using cold hammer and a pestle. The pestle was placed over dry ice to maintain it at low temperatures. The ground tumor was suspended in ice-cold PBS and dounce homogenized and subsequently washed twice with ice-cold PBS. The cell pellets obtained from and washed xenografts were processed similar to the pellets obtained from in-vitro experiments (RNA-seq protocol). Hormone-treated cells were homogenized and total RNA was extracted using Qiagen RNAeasy kit. PolyA tail selection was performed on 250 ng of total RNA. RNA-seq libraries were prepared using NEBNext kit. Details of library preparation strategy are provided in the materials and methods section (RNA expression and RNA-sequencing) of the paper. NextSeq 500 gds 302648132 GSM2648132 GEO Accession GSM2648132