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Series GSE68827 Query DataSets for GSE68827
Status Public on Jun 25, 2015
Title Leukemia Inhibitory Factor in C26 Cancer Cachexia
Organism Mus musculus
Experiment type Expression profiling by array
Summary Cachexia is an exacerbating event in many types of cancer that is strongly associated with a poor prognosis. We have identified cytokine, signaling and transcription factors that are required for cachexia in the mouse C26 colon carcinoma model of cancer. C2C12 myotubes treated with conditioned medium from C26 cancer cells induced atrophy and activated a STAT-dependent reporter gene but not reporter genes dependent on SMAD, FOXO, C/EBP, NF-ĸB, or AP-1. Of the gp130 family members IL-11, IL-6, oncostatin M (OSM), and leukemia inhibitory factor (LIF), only OSM and LIF were sufficient to activate the STAT reporter in myotubes. A LIF blocking antibody abolished C26 CM-induced STAT reporter activation STAT3 phosphorylation and myotube atrophy, but blocking antibodies to IL-6 or OSM did not. JAK2 inhibitors also blocked the C26 CM-induced STAT reporter activation, STAT3 phosphorylation, and atrophy in myotubes. LIF at levels found in the C26 CM was sufficient for STAT reporter activation and atrophy in myotubes. In vivo, an increase in serum LIF preceded the increase in IL-6 in mice with C26 tumors. Overexpression of a dominant negative Stat3Cβ-EGFP gene in myotubes and in mouse muscle blocked the atrophy caused by C26 CM or C26 tumors, respectively. Taken together these data support an important role of LIF- JAK2-STAT3 in C26 cachexia and point to a therapeutic approach for at least some types of cancer cachexia.
 
Overall design from three replicate wells of cells at each treatment, pools of total RNA were used to create cDNA which were evaluated on Affymetrix mouse gene 1.0 ST v.1 arrays.
 
Contributor(s) Seto DN, Kandarian SC, Jackman RW
Citation(s) 26092726
Submission date May 13, 2015
Last update date Jun 25, 2015
Contact name Robert William Jackman
E-mail(s) rjackman@bu.edu
Phone 6173532719
Organization name Boston University (BU)
Department Health Sciences
Street address 635 Commonwealth Avenue/rm 444
City Boston
State/province Massachusetts
ZIP/Postal code 02215
Country USA
 
Platforms (1)
GPL19485 [MoGene-1_0-st] Affymetrix Mouse Gene 1.0 ST Array [CDF: MoGene10stv1_Mm_ENTREZG_16.0.0]
Samples (12)
GSM1682574 LIF 4 hour C
GSM1682575 LIF 4 hour E
GSM1682576 LIF 8 hour C
Relations
BioProject PRJNA283877

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
GSE68827_C26CM_4h_8h_24h_foldchange.txt.gz 799.0 Kb (ftp)(http) TXT
GSE68827_LIF_2015-03-12_4h_8h_foldchange.txt.gz 2.0 Mb (ftp)(http) TXT
GSE68827_LIF_2015-04-30_24h_foldchange.txt.gz 2.1 Mb (ftp)(http) TXT
GSE68827_RAW.tar 69.9 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table
Processed data are available on Series record

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