NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE41559 Query DataSets for GSE41559
Status Public on May 31, 2013
Title Expression data by telomere elongation in vivo (xenograft)
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Limitless reproductive potential is one of the hallmarks of cancer cells1. This ability is accomplished by maintaining telomeres, which erosion otherwise causes cellular senescence or death. Human cancer cells often maintain shorter telomeres than do cells in surrounding normal tissues2-5. While most cancer cells activate telomerase, which can elongate telomeres6, it remains elusive why cancer cells keep telomeres short. Here we show that forced elongation of telomeres in cancer cells promotes their differentiation in a tumor microenvironment in vivo. We elongated telomeres of human prostate cancer PC-3 cells, which possess short telomeres7, by enhancing their telomerase activity. The resulting cells with long telomeres retain an ability to form tumors in a mouse xenograft model. Strikingly, these tumors exhibit many duct-like structures and reduced N-cadherin expression, reminiscent of well-differentiated adenocarcinoma. These phenotypic changes are caused by telomere elongation per se but not enhanced telomerase activity. Gene expression profiling revealed that telomere elongation correlates with inhibition of cell-cycle processes. Together, our results suggest a functional contribution of short telomeres to tumor malignancy by regulating cancer cell differentiation.
 
Overall design Two cell lines are telomere-elongated cells, both in the presence and absence of the exogenous hTERT. The other two lines are control PC-3 cell lines. We extracted RNA from four independent xenograft tumors per original cell line.
 
Contributor(s) Hirashima K, Seimiya H
Citation(s) 23716593
Submission date Oct 12, 2012
Last update date Mar 25, 2019
Contact name kyotaro HIRASHIMA
Organization name The JFCR-Cancer Inst.
Department Cancer Chemotherapy Center
Lab Division of Molecular Biotherapy
Street address 3-8-31 Ariake
City Koto-ku
State/province Tokyo
ZIP/Postal code 135-8550
Country Japan
 
Platforms (1)
GPL570 [HG-U133_Plus_2] Affymetrix Human Genome U133 Plus 2.0 Array
Samples (16)
GSM1019098 PC-3_basalhTERT_ShortTelomeres_mock_1
GSM1019099 PC-3_basalhTERT_ShortTelomeres_mock_2
GSM1019100 PC-3_basalhTERT_ShortTelomeres_mock_3
Relations
BioProject PRJNA177428

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
GSE41559_RAW.tar 77.0 Mb (http)(custom) TAR (of CEL)
GSE41559_matrix_with_annotations.txt.gz 5.2 Mb (ftp)(http) TXT
Processed data included within Sample table
Processed data are available on Series record

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