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Series GSE125743 Query DataSets for GSE125743
Status Public on May 29, 2019
Title Fractional Deletion of Compound Kushen Injection Indicates Cytokine Signaling Pathways are Critical for its Perturbation of the Cell Cycle
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary We have used computational and experimental biology approaches to identify candidate mechanisms of action of a traditional Chinese medicine; Compound Kushen Injection (CKI), in a breast cancer cell line in which CKI has been shown to cause apoptosis. Because CKI is a complex mixture of plant secondary metabolites, we used a high-performance liquid chromatography (HPLC) fractionation and reconstitution approach to define chemical fractions required for CKI to induce apoptosis in MDA-MB-231 cells. Our initial fractionation separated major from minor compounds, and showed that the major compounds accounted for little of the activity of CKI. By systematically perturbing the major compounds in CKI we found that removal of no single major compound could alter the effect of CKI on cell viability and apoptosis. However, simultaneous removal of two major compounds identified oxymatrine and oxysophocarpine as critical compounds with respect to CKI activity. We then used RNA sequencing and transcriptome analysis to correlate compound removal with gene expression and phenotype data. We determined that many compounds in CKI are required for its effectiveness in triggering apoptosis but that significant modulation of its activity is conferred by a small number of compounds. In conclusion, CKI may be typical of many plant based extracts that contain many compounds in that no single compound is responsible for all of the bioactivity of the mixture and that many compounds interact in a complex fashion to influence a network containing many targets.
 
Overall design High-depth paired-end RNA-seq from MDA-MB-231 cell line. Each sample contains 3 biological replicates. N_2(where N represents the total number of compounds in CKI, N_2 represents removal of Omt and Ospc from CKI which is N-OmtOspc), N_3 represents removal of Mac, Omt and Ospc from CKI (hence N-MacOmtOspc), OO represents two compounds only: Omt and Ospc, MOO represents three compounds only: Mac, Omt and Ospc, N_Mac represents removal of Mac from CKI (hence N-Mac), N_Nme represents removal of Nme from CKI, N_Omt represents removal of Omt from CKI, and N_Tri represents removal of Tri from CKI. See the manuscript doi: https://0-doi-org.brum.beds.ac.uk/10.1101/462135 for more details.
 
Contributor(s) Aung TN, Adelson DL
Citation(s) 31106149, 31578346
Submission date Jan 28, 2019
Last update date Oct 15, 2019
Contact name Thazin Nwe Aung
E-mail(s) thazin.nweaung@adelaide.edu.au
Organization name University of Adelaide
Lab Adelson
Street address Frome
City Adelaide
State/province South Australia
ZIP/Postal code 5005
Country Australia
 
Platforms (1)
GPL20795 HiSeq X Ten (Homo sapiens)
Samples (54)
GSM3581341 24h_UT1_Rep1_Batch1
GSM3581342 24h_UT2_Rep2_Batch1
GSM3581343 24h_UT3_Rep3_Batch1
Relations
BioProject PRJNA517432
SRA SRP182663

Download family Format
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Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE125743_refGenes_raw_count.txt.gz 1.7 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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