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Series GSE140440 Query DataSets for GSE140440
Status Public on Sep 01, 2020
Title Single Cell Analysis Reveals NUPR1 Promotes Docetaxel Resistance in Prostate Cancer
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary The majority of prostate cancer (PCa) patients treated with docetaxel develop resistance to it. In order to better understand the mechanism behind the acquisition of resistance, we conducted single cell total RNA sequencing (sctotal RNA-seq) of docetaxel sensitive and resistant variants of DU145 and PC3 PCa cell lines. Overall, sensitive and resistant cells clustered separately. However, for both cell lines we identified rare sensitive cells that clustered with the resistant cells indicating resistant cells pre-exist in the sensitive population. Differential gene expression analysis between resistant and sensitive cells revealed 182 differentially expressed genes common to both PCa cell lines. A subset of these genes gave a gene expression profile in the resistant-like sensitive cells similar to the resistant cells. Exploration for functional gene pathways identified 218 common pathways between the two cell lines. Protein ubiquitination was the most differentially regulated pathway and was enriched in the resistant cells. Transcriptional regulator analysis identified potential 321 regulators across both cell lines. One of the top regulators identified was nuclear protein 1 (NUPR1). In contrast to the single cell analysis, bulk analysis of the cells did not reveal NUPR1 as a promising candidate. Knockdown and overexpression of NUPR1 in the PCa cells demonstrated that NUPR1 confers docetaxel resistance in both cell lines. Collectively, these data demonstrate the utility of sctotal RNA-seq to identify regulators of drug resistance. Furthermore, NUPR1 was identified as a mediator of PCa drug resistance, which provides the rationale to explore NUPR1 and its target genes to for reversal of docetaxel resistance.
 
Overall design Single cell sequencing of DU145 and PC3 sensitive and docetaxel resistant cell lines
 
Contributor(s) Schnepp PM, Shelley G, Wakim N, Jiang H, Mizokami A, Keller ET
Citation(s) 32513898
Submission date Nov 15, 2019
Last update date Sep 01, 2020
Contact name Evan T Keller
E-mail(s) etkeller@med.umich.edu
Organization name University of Michigan
Street address 2800 Plymouth Rd
City Ann Arbor
State/province MI
ZIP/Postal code 48109
Country USA
 
Platforms (2)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
GPL20301 Illumina HiSeq 4000 (Homo sapiens)
Samples (324)
GSM4161452 DU145_Sen_1
GSM4161453 DU145_Sen_2
GSM4161454 DU145_Sen_3
Relations
BioProject PRJNA589746
SRA SRP230181

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Supplementary file Size Download File type/resource
GSE140440_RAW.tar 165.5 Mb (http)(custom) TAR (of TXT)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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