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Series GSE45265 Query DataSets for GSE45265
Status Public on Dec 31, 2014
Title Effect of lentiviral-based shRNA-mediated knockdown of ZFX on the human medulloblastoma (MB) cell-line DAOY
Organism Homo sapiens
Experiment type Expression profiling by array
Summary The Hedgehog (Hh) signaling pathway regulates normal development and cell proliferation, whereas its aberrant activation causes tumor formation. Hh-induced tumors can arise from different tissues and can be indolent or highly aggressive, such as basal cell carcinoma (BCC) of the skin and neural progenitor-derived medulloblastoma (MB), respectively. Little is known about cell-intrinsic factors that control the development of such diverse Hh-dependent tumors. Transcription factor Zfx is required for the self-renewal of several stem cell types, whereas its role in malignant transformation remains controversial. We found that the deletion of Zfx prevented BCC formation and significantly delayed MB development caused by Hh activation in vivo. In contrast, Zfx was dispensable for the development of Hh-independent brain tumor glioblastoma. We used genome-wide expression and chromatin binding analysis in a human MB cell line to identify direct, evolutionarily conserved targets of Zfx. These targets included the Hh signal transducer Smoothened (Smo), suggesting that Zfx may directly control Hh pathway activation in tumors. Two additional targets of Zfx, Dis3L and Ube2j1, were also required for the growth of MB cells in vitro. These results identify a common cell-intrinsic regulator of diverse Hh-induced tumors, and suggest Zfx and Zfx-controlled genes as possible therapeutic targets in these malignancies.
 
Overall design DAOY cells were transduced for 16-24 hours with lentivirus encoding shRNA targeting ZFX (H2, H3, H4) or scrambled non-targeting shRNA (SCR). Cells were allowed to recover for 48 hours, and then were replated in 2 ug/mL puromycin selective media. Cells were collected in TriZol LS reagent for RNA for microarrays ~48 hours after start of puromycin selection.
 
Contributor(s) Palmer CJ, Reizis BV
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Submission date Mar 18, 2013
Last update date Jul 26, 2018
Contact name Colin Palmer
E-mail(s) cjp2123@columbia.edu
Organization name Columbia University
Department Microbiology & Immunology
Lab Reizis Lab
Street address 701 W. 168th Street
City New York
State/province New York
ZIP/Postal code 10032
Country USA
 
Platforms (1)
GPL6244 [HuGene-1_0-st] Affymetrix Human Gene 1.0 ST Array [transcript (gene) version]
Samples (4)
GSM1100337 DAOY_H2
GSM1100338 DAOY_H3
GSM1100339 DAOY_H4
This SubSeries is part of SuperSeries:
GSE45396 Transcription factor ZFX
Relations
BioProject PRJNA193340

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
GSE45265_RAW.tar 18.6 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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