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Series GSE264131 Query DataSets for GSE264131
Status Public on Jul 26, 2024
Title Comparative network-based analysis of toll-like receptor agonist, L-pampo signaling pathways in immune and cancer cells
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Toll-like receptors (TLRs) are critical immune components to stimulate immune responses against various infections. Recently, TLR agonists have emerged as a promising way to activate anti-tumor immunity. L-pampo, a TLR1/2 and TLR3 agonist, induces robust humoral and cellular immune responses but also causes cancer cell death. In this study, we investigated the L-pampo-induced signal pathways in immune and cancer cells and how they interact with TLRs and cancer-related pathways. First, we constructed a template network with differentially expressed genes and influential genes using the weighted gene co-expression network analysis (WGCNA). Next, we obtained perturbed modules using the same method and extracted core subnetworks from the modules by running Walktrap. Finally, we attempted to link the core subnetworks for reconstructing major molecular signals regarding the response to L-pampo utilizing a shortest path finding algorithm, TOPAS. Our analysis revealed that the key molecular processes were PI3K-AKT, JAK-STAT, and oxidative phosphorylation (OXPHOS) with reactive oxygen species (ROS) in immune and cancer cells. Notably, the OXPHOS process may be the crucial regulator for the differential responses of L-pampo between cancer cells of different tissue types. Our computational approaches can be applied to similar research for inferring underlying molecular mechanisms using complex gene expression profiles.
 
Overall design To determine whether L-pampo drives the differential responses of cellular networks in different cell types, we chose a differentiated human monocyte cell line, THP-1, that highly expresses TLR2/3 and induces various immune responses to L-pampo. Additionally, we utilized two cancer cell lines, PC-3 and SW620, that can express TLR2/3 but manifest differential responses by L-pampo treatment. Then, we investigated gene signatures associated with L-pampo in immune cells and cancer cells using RNA-seq and various computational methods.
 
Contributor(s) Kim G, Chun E, Yum JS
Citation(s) 39060412
Submission date Apr 16, 2024
Last update date Oct 27, 2024
Contact name Sera Park
E-mail(s) sera.park@mogam.re.kr
Organization name MOGAM Institute for Biomedical Research
Street address 15-19 Gangnam-daero 41-gil
City Seoul
State/province Seocho-gu
ZIP/Postal code 06730
Country South Korea
 
Platforms (1)
GPL24676 Illumina NovaSeq 6000 (Homo sapiens)
Samples (27)
GSM8212612 differentiated THP-1 (monocyte) cells, Non-treatment, 0 hour, replicate 1
GSM8212613 differentiated THP-1 (monocyte) cells, Non-treatment, 0 hour, replicate 2
GSM8212614 differentiated THP-1 (monocyte) cells, Non-treatment, 0 hour, replicate 3
Relations
BioProject PRJNA1101035

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
GSE264131_tpm.csv.gz 1.0 Mb (ftp)(http) CSV
SRA Run SelectorHelp
Raw data are available in SRA

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