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Series GSE71898 Query DataSets for GSE71898
Status Public on Dec 09, 2015
Title AKT Inhibition Promotes Non-autonomous Cancer Cell Survival [GRO-Seq]
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Other
Summary Small-molecule inhibitors of AKT signaling are being in evaluated in patients with various cancer types, but have so far proven therapeutically disappointing for reasons that remain unclear. Here, we treat cancer cells with sub-therapeutic doses of Akti-1/2, an allosteric small molecule AKT inhibitor, in order to experimentally model pharmacologic inhibition of AKT signaling in vitro. We then apply a combined RNA, protein, and metabolite profiling approach to develop an integrated, multi-scale, molecular snapshot of this “AKTlow” cancer cell state. We find that AKT-inhibited cancer cells suppress thousands of mRNA transcripts, and proteins related to the cell cycle, ribosome, and protein translation. Surprisingly, however, these AKT-inhibited cells simultaneously up-regulate a host of other proteins and metabolites post-transcriptionally, reflecting activation of their endo-vesiculo-membrane system, secretion of inflammatory proteins, and elaboration of extracellular microvesicles. Importantly, these microvesicles enable rapidly proliferating cancer cells of various types to better withstand different stress conditions, including serum deprivation, hypoxia, or cytotoxic chemotherapy in vitro and xenografting in vivo. These findings suggest a model whereby cancer cells experiencing a partial inhibition of AKT signaling may actually promote the survival of neighbors through non-cell autonomous communication.
 
Overall design Profiles of MCF7 and HCT116 Akti-1/2 treated cells and MCF7 and HCT116 vehicle (i.e. DMSO) treated cells were generated, each in duplicate, using GRO-Seq.
 
Contributor(s) Sole X, Salony ., Alves CP, Dey-Guha I, Ritsma L, Boukhali M, Lee JH, Chowdhury J, Ross KN, Haas W, Vasudevan S, Ramaswamy S
Citation(s) 26637368
Submission date Aug 10, 2015
Last update date May 15, 2019
Contact name Ben S Wittner
E-mail(s) wittner.ben@mgh.harvard.edu
Phone +1-617-643-3166
Organization name Massachusetts General Hospital
Department Cancer Center
Lab Sridhar Ramaswamy's Lab
Street address 185 Cambridge Street
City Boston
State/province MA
ZIP/Postal code 02114
Country USA
 
Platforms (1)
GPL11154 Illumina HiSeq 2000 (Homo sapiens)
Samples (8)
GSM1847251 MCF7_Akti1/2_Replicate1 (GRO-Seq)
GSM1847252 MCF7_Akti1/2_Replicate2 (GRO-Seq)
GSM1847253 MCF7_DMSO_Replicate1 (GRO-Seq)
This SubSeries is part of SuperSeries:
GSE71901 AKT Inhibition Promotes Non-autonomous Cancer Cell Survival
Relations
BioProject PRJNA292421
SRA SRP062229

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
GSE71898_RPKMs_Excluding_First_500bp_Downstream_TSS.txt.gz 981.2 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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