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Series GSE216043 Query DataSets for GSE216043
Status Public on Mar 20, 2023
Title Genome-scale CRISPR screen reveals neddylation to contribute to cisplatin resistance of testicular germ cell tumors
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Type II testicular germ cell tumors (TGCT) are the most prevalent tumors in young men. Patients suffering from cisplatin resistant TGCTs are facing very poor prognosis demanding novel therapeutic options. Neddylation is a known posttranslational modification mediating many important biological processes including tumorigenesis. Overactivation of neddylation pathway promotes carcinogenesis and tumor progression in various entities by inducing proteasomal degradation of tumor suppressors (e.g., p21, p27). We used a genome-scale CRISPR/Cas9 activation screen to identify cisplatin resistance factors. TGCT cell lines were treated with the neddylation inhibitor (MLN4924)/cisplatin/combination and investigated for changes in viability (XTT assay), apoptosis/cell cycle (flow cytometry) as well as in the transcriptome (3’mRNA sequencing). NAE1 overexpression was detected in cisplatin resistant colonies from the CRISPR screen. Inhibition of neddylation using MLN4924 increased cisplatin cytotoxicity in TGCT cell lines and sensitized cisplatin resistant cells towards cisplatin. Apoptosis, G2/M-phase cell cycle arrest, gH2A.X/P27 accumulation and mesoderm/endoderm differentiation was observed in TGCT cells while fibroblast cells were unaffected. We identified overactivation of neddylation as a factor for cisplatin resistance in TGCTs and highlighted the additive effect of NAE1 inhibition by MLN4924 in combination with cisplatin as a novel treatment option for TGCTs.
 
Overall design Total RNA obtained from cell lines treated for 48 hours with MLN4924 only/cisplatin only/combination (MLN4924 and cisplatin) compared to DMSO/DMF/combination (DMSO and DMF) treated control cells. Total 36 samples with n=3 for each condition.
 
Contributor(s) Funke K, Einsfelder U, Hansen A, Arévalo L, Schneider S, Nettersheim D, Stein V, Schorle H
Citation(s) 37024667
Submission date Oct 18, 2022
Last update date Apr 12, 2023
Contact name Kai Funke
Organization name University Hospital Bonn
Department Pathology, Developmental Pathology
Street address Venusberg-Campus 1
City Bonn
State/province NRW
ZIP/Postal code 53127
Country Germany
 
Platforms (1)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
Samples (36)
GSM6657672 2102EP, MLN4924, 1
GSM6657673 2102EP, MLN4924, 2
GSM6657674 2102EP, MLN4924, 3
Relations
BioProject PRJNA891754

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE216043_2102EP_Cisplatin_vs_DMF_DESeq2_DE.txt.gz 1009.2 Kb (ftp)(http) TXT
GSE216043_2102EP_Cisplatin_vs_DMF_DESeq2_counts.txt.gz 1.3 Mb (ftp)(http) TXT
GSE216043_2102EP_MLN4924_vs_DMSO_DESeq2_DE.txt.gz 940.7 Kb (ftp)(http) TXT
GSE216043_2102EP_MLN4924_vs_DMSO_DESeq2_counts.txt.gz 1.3 Mb (ftp)(http) TXT
GSE216043_2102EP_MLN_CP_vs_DMSO_DMF_DESeq2_DE.txt.gz 979.7 Kb (ftp)(http) TXT
GSE216043_2102EP_MLN_CP_vs_DMSO_DMF_DESeq2_counts.txt.gz 1.3 Mb (ftp)(http) TXT
GSE216043_JAR_Cisplatin_vs_DMF_DESeq2_DE.txt.gz 777.9 Kb (ftp)(http) TXT
GSE216043_JAR_Cisplatin_vs_DMF_DESeq2_counts.txt.gz 1.3 Mb (ftp)(http) TXT
GSE216043_JAR_MLN4924_vs_DMSO_DESeq2_DE.txt.gz 885.0 Kb (ftp)(http) TXT
GSE216043_JAR_MLN4924_vs_DMSO_DESeq2_counts.txt.gz 1.3 Mb (ftp)(http) TXT
GSE216043_JAR_MLN_CP_vs_DMSO_DMF_DESeq2_DE.txt.gz 891.3 Kb (ftp)(http) TXT
GSE216043_JAR_MLN_CP_vs_DMSO_DMF_DESeq2_counts.txt.gz 1.3 Mb (ftp)(http) TXT
GSE216043_MLN_CP_stringtie_raw_counts.csv.gz 1.2 Mb (ftp)(http) CSV
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Processed data are available on Series record

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