NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE219229 Query DataSets for GSE219229
Status Public on Apr 16, 2024
Title Unbiased profiling of clinical kinase inhibitors’ effects in activated macrophages using chromatin modifications as high-content readouts [RNA-Seq]
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary More than 500 kinases are implicated in the control of virtually every cellular process in mammals and deregulation of their activity is causally linked to diseases ranging from cancer to inflammatory and degenerative disorders. In the last three decades, massive worldwide efforts led to the approval of 62 clinical kinase inhibitors (CKI), with hundreds of additional molecules in various stages of pre-clinical or clinical development. In addition to the intended target(s), small molecule CKI commonly inhibit multiple additional kinases, resulting in both enhanced clinical effects and undesired side effects that are largely unpredictable based on in vitro selectivity profiling. To complement current CKI profiling methods, we set out a novel experimental and analytical approach grounded on the use of chromatin modifications as unbiased and information-rich readouts of the functional effects of CKI on macrophage activation, a complex biological response of biomedical relevance. This approach allowed us to characterize and dissect the distinctive behaviors of CKI with identical intended targets as well as to discover undescribed activities of CKI on macrophage activation programs.
 
Overall design PolyA RNAseq of mouse bone marrow-derived macrophages (BMDM) were pre-treated with DMSO or the individual Kinase Inhibitors for 1h and then stimulated with LPS for 2h.
 
Contributor(s) Gualdrini F, Rizzieri S, Pileri F, Polletti S, Natoli G
Citation(s) 38724853
Submission date Dec 02, 2022
Last update date Jun 26, 2024
Contact name Francesco Gualdrini
E-mail(s) Francesco.gualdrini@ieo.it
Organization name European Institute of Oncology
Department Department of Experimental Oncology
Lab Transcriptional Control in Inflammation and Cancer
Street address Via Adamello, 16
City Milan
ZIP/Postal code 20139
Country Italy
 
Platforms (1)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
Samples (180)
GSM6778161 AC480_2hLPS_R1
GSM6778162 AC480_2hLPS_R2
GSM6778163 AC480_2hLPS_R3
This SubSeries is part of SuperSeries:
GSE219240 Unbiased profiling of clinical kinase inhibitors’ effects in activated macrophages using chromatin modifications as high-content readouts
Relations
BioProject PRJNA907768

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
GSE219229_Normalized_exonic_readcounts.txt.gz 7.0 Mb (ftp)(http) TXT
GSE219229_RAW.tar 7.5 Gb (http)(custom) TAR (of BW)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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