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Status |
Public on Nov 06, 2013 |
Title |
Disulphide bond inhibitors in 2 cancer cell lines |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array
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Summary |
To elucidate which ER cargo maturation processes may be oxygen dependent, we first reasoned that the transcriptional response may be tailored specifically to counteract the mechanism of the imposed stress. Therefore, we compared the transcriptional regulation of the ERome during anoxic conditions to ER stress caused by lack of glycosylation (tunicamycin) or chaperone inactivation by calcium depletion (thapsigargin)
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Overall design |
In two cancer cell lines (colon carcinoma HCT116, and hepatocellular carcinoma Hep G2) cells were given one of 4 treatments. 24 hours of 0.0% O2 (Anoxia), 1.5 µg/ml tunicamycin or 0.3 µM thapsigargin with a control 21% O2 (Normoxia). Cells were exposed to hypoxia and anoxia in H35 and H85 HypOxystations (Don Whitley Scientific). 3 biological replicates of each experiment were carried out. Total of 24 samples.
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Contributor(s) |
Koritzinsky M, van den Beucken T, Harding NJ, Chu K, Boutros PC, Braakman I, Wouters BG |
Citation(s) |
24247433 |
Submission date |
Oct 17, 2012 |
Last update date |
Aug 13, 2018 |
Contact name |
Nicholas J Harding |
E-mail(s) |
nicholas.harding@oicr.on.ca
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Phone |
4167320720
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Organization name |
OICR
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Department |
Informatics and Biocomputing Platform
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Lab |
Boutros
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Street address |
101 College St
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City |
Toronto |
State/province |
ON |
ZIP/Postal code |
M5G 0A3 |
Country |
Canada |
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Platforms (1) |
GPL10558 |
Illumina HumanHT-12 V4.0 expression beadchip |
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Samples (24)
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Relations |
BioProject |
PRJNA177853 |