NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE130359 Query DataSets for GSE130359
Status Public on Aug 20, 2019
Title A new strategy for identifying mechanisms of drug-drug interaction using transcriptome analysis: Compound Kushen injection as a proof of principle
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Drug-drug interactions (DDIs), especially with herbal medicines, are complex, making it difficult to identify potential molecular mechanisms and targets. We introduce a workflow to carry out DDI research using transcriptome analysis and interactions of a complex herbal mixture, Compound Kushen Injection (CKI), with cancer chemotherapy drugs, as a proof of principle. Using CKI combined with doxorubicin or 5-Fu on cancer cells as a model, we found that CKI enhanced the cytotoxic effects of doxorubicin on A431 cells while protecting MDA-MB-231 cells treated with 5-Fu. We generated and analysed transcriptome data from cells treated with single treatments or combined treatments and our analysis showed that opposite directions of regulation for pathways related to DNA synthesis and metabolism appeared to be the main reason for different effects of CKI when used in combination with chemotherapy drugs . We also found that pathways related to organic biosynthetic and metabolic processes might be potential targets for CKI when interacting with doxorubicin and 5-Fu. Through co-expression analysis correlated with phenotype results, we selected the MYD88 gene as a candidate major regulator for validation as a proof of concept for our approach. Inhibition of MYD88 reduced antagonistic cytotoxic effects between CKI and 5-Fu, indicating that MYD88 is an important gene in the DDI mechanism between CKI and chemotherapy drugs. These findings demonstrate that our pipeline is effective for the application of transcriptome analysis to the study of DDIs in order to identify candidate mechanisms and potential targets.
 
Overall design High-depth paired-end RNA-seq from A431 epidermoid carcinoma cell line and MDA-MB 231 adenocarcinoma cell line. Each sample contains 3 biological replicates.
 
Contributor(s) Shen H, Adelson DL
Citation(s) 31380274, 31685921
Submission date Apr 26, 2019
Last update date Nov 19, 2019
Contact name David L. Adelson
E-mail(s) david.adelson@adelaide.edu.au
Organization name University of Adelaide
Department Molecular and biomedical science
Street address University of Adelaide
City Adelaide
State/province South Australia
ZIP/Postal code 5005
Country Australia
 
Platforms (1)
GPL20795 HiSeq X Ten (Homo sapiens)
Samples (27)
GSM3736781 48h_untreated_A431_1
GSM3736782 48h_untreated_A431_2
GSM3736783 48h_untreated_A431_3
Relations
BioProject PRJNA539875
SRA SRP193948

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
GSE130359_EGID_samples.csv.gz 994.9 Kb (ftp)(http) CSV
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap