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Series GSE5824 Query DataSets for GSE5824
Status Public on Sep 14, 2006
Title Identification of rapamycin as a glucocorticoid resistance reversal agent
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Drug resistance remains a major obstacle to successful cancer treatment. Here we use a novel approach to identify rapamycin as a glucocorticoid resistance reversal agent. A database of drug-associated gene expression profiles was screened for molecules whose profile overlapped with a gene expression signature of glucocorticoid (GC) sensitivity/resistance in Acute Lymphoblastic Leukemia (ALL) cells. The screen indicated the mTOR inhibitor rapamycin profile matched the signature of GC-sensitivity. We thus tested the hypothesis that rapamycin would induce GC sensitivity in lymphoid malignancy cells, and found that it sensitized cells to glucocorticoid induced apoptosis via modulation of antiapoptotic MCL1. These data indicate that MCL1 is an important regulator of GC-induced apoptosis, and that the combination of rapamycin and glucocorticoids has potential utility in ALL. Furthermore this approach represents a novel strategy for identification of promising combination therapies for cancer.

This SuperSeries is composed of the SubSeries listed below.
 
Overall design Refer to individual Series
 
Citation(s) 17010674
Submission date Sep 13, 2006
Last update date Aug 10, 2018
Contact name Scott A. Armstrong
E-mail(s) [email protected]
Phone 617-919-2508
Fax 617-730-0934
Organization name Children's Hospital
Department Hematology/Oncology
Street address 1 Blackfan Circle
City Boston
State/province MA
ZIP/Postal code 02115
Country USA
 
Platforms (1)
GPL96 [HG-U133A] Affymetrix Human Genome U133A Array
Samples (38)
GSM135892 sensitive sample 1
GSM135893 Sensitive sample 2
GSM135894 sensitive sample 3
This SuperSeries is composed of the following SubSeries:
GSE5820 Gene expression-based chemical genomics identifies rapamycin as a modulator of MCL-1 and glucocorticoid resistance
GSE5821 Rapamycin treatment of CEM_C1 cells 24 hours
GSE5822 Rapamycin treated CEM-C1 cells 3 hours
Relations
BioProject PRJNA97211

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