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SRX24336217: GSM8222915: Human Prostate Biopsy, HMP23A; Homo sapiens; RNA-Seq
2 ILLUMINA (Illumina NovaSeq 6000) runs: 271.2M spots, 32.5G bases, 10.3Gb downloads

External Id: GSM8222915_r1
Submitted by: Memorial Sloan Kettering Cancer Center
Study: Single Cell Analysis of Treatment–Resistant Prostate Cancer: Implications of Cell State Changes for Cell Surface Antigen Targeted Therapies
show Abstracthide Abstract
Targeting cell surface molecules using radioligand and antibody–based therapies has yielded considerable success across cancers. However, it remains unclear how the expression of putative lineage markers, particularly cell surface molecules, varies in the process of lineage plasticity, wherein tumor cells alter their identity and acquire new oncogenic properties. A notable example of lineage plasticity is the transformation of prostate adenocarcinoma (PRAD) to neuroendocrine prostate cancer (NEPC)––a growing resistance mechanism that results in the loss of responsiveness to androgen blockade and portends dismal patient survival. To understand how lineage markers vary across the evolution of lineage plasticity in prostate cancer, we applied single cell analyses to 21 human prostate tumor biopsies and two genetically engineered mouse models, together with tissue microarray analysis (TMA) on 131 tumor samples. Not only did we observe a higher degree of phenotypic heterogeneity in castrate–resistant PRAD and NEPC than previously anticipated, but also found that the expression of molecules targeted therapeutically, namely PSMA, STEAP1, STEAP2, TROP2, CEACAM5, and DLL3, varied within a subset of gene–regulatory networks (GRNs). We also noted that NEPC and small cell lung cancer (SCLC) subtypes shared a set of GRNs, indicative of conserved biologic pathways that may be exploited therapeutically across tumor types. While this extreme level of transcriptional heterogeneity, particularly in cell surface marker expression, may mitigate the durability of clinical responses to novel antigen–directed therapies, its delineation may yield signatures for patient selection in clinical trials, potentially across distinct cancer types. Overall design: Tumor biopsies were dissociated per previously published protocols (PMID: 35981096). Single cell data for HMP22, HMP23A, HMP23B, HMP24 has not previously been published and is deposited under this GEO ID. Data for HMP04, HMP05, HMP08, HMP11A, HMP11B, HMP13, HMP14, HMP16, HMP17, HMP19, HMP20, HMP25, and HMP26 were re–analyzed, but has previously been published in the context of JAK/STAT signaling in prostate cancer under GSE210358 (PMID 35981096). Data from HP95, HP96, HP97, HP99, HP100, and HP101 are also re–analyzed and has previously been published by our group in the context luminal regeneration under https://duos.broadinstitute.org/ (accession no. DUOS-000115). We have also included processed RDS files for combined samples (N=23) for all cells and tumor cells. Of note, HP and HMP IDs correspond to MSK–HP IDs as presented in this publication in Supplementary Table 3. The list of the re-analyzed sample in GSE210358: SRX16781303 GSM6428952 HMP04 SAMN30111353 SRX16781304 GSM6428953 HMP05 SAMN30111352 SRX16781305 GSM6428954 HMP08 SAMN30111351 SRX16781314 GSM6428955 HMP11_1 SAMN30111350 SRX16781315 GSM6428956 HMP11_2 SAMN30111349 SRX16781316 GSM6428957 HMP13 SAMN30111348 SRX16781317 GSM6428958 HMP14 SAMN30111347 SRX16781319 GSM6428960 HMP16 SAMN30111345 SRX16781318 GSM6428959 HMP15 SAMN30111346 SRX16781320 GSM6428961 HMP17 SAMN30111344 SRX16781321 GSM6428962 HMP19 SAMN30111343 SRX16781322 GSM6428963 HMP20 SAMN30111342 SRX16781323 GSM6428964 HMP25 SAMN30111341 SRX16781325 GSM6428965 HMP26 SAMN30111340
Sample: Human Prostate Biopsy, HMP23A
SAMN41047768 • SRS21096394 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: GSM8222915
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC SINGLE CELL
Selection: cDNA
Layout: PAIRED
Construction protocol: Fresh benign and malignant tissue was mechanically cut using a scalpel into small pieces (~1–5 mm3). The tissue was then processed and dissociated in 5–10 mg/ml collagenase type II (Gibco) solution in adDMEM/F12+/+/+ with 10 µM Y–27632 dihydrochloride for 30 minutes to 2 hours on a 37oC shaking platform. This was followed by a 1 minute 0.5 M EDTA wash at room temperature, and subsequent digestion with TrypLE (Gibco) with 10 µM Y–27632 dihydrochloride for 5–10 minutes at 37oC on a shaking platform until a single cell suspension was obtained. If more than 10% of doublets were present (visual inspection) or there was evidence for <80% viability (hemocytometer, using 0.2% Trypan Blue), then cells were FACS–sorted for singlets and viability using a DAPI. Please refer to methods of paper for further details. Dissociated cells were subjected to scRNA–seq using 10X genomics Chromium Single Cell 3' Library and Gel bead Kit (v3 for all human biospies, except v2 for HP95T as previously described PMID: 32355025) per manufacturer's protocol. ~3000 to 10,000 cells per sample was encapsulated and barcoded following the manual. Sample viability varied between 72 and 95% (0.2% Trypan Blue). The final sequencing libraries were double–size purified (0.6–0.8X) with SPRI beads and sequenced on Illumina Nova–Seq platform (R1–26 cycles, i7–8 cycles, R2–70 cycles or higher).
Runs: 2 runs, 271.2M spots, 32.5G bases, 10.3Gb
Run# of Spots# of BasesSizePublished
SRR28771043135,612,72316.3G5.1Gb2024-05-20
SRR28771044135,600,00616.3G5.1Gb2024-05-20

ID:
32650288

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