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Series GSE6020 Query DataSets for GSE6020
Status Public on Nov 15, 2006
Title MiRNA Expression data from Tk6 cell treated with arsenic, gamma-IR, or grown under folate-deficiency
Platform organisms Homo sapiens; Mus musculus; Rattus norvegicus
Sample organism Homo sapiens
Experiment type Non-coding RNA profiling by array
Summary Folate deficiency, arsenic exposure, and gamma-IR are known developmental toxicants and have carcinogenic effects. The mechanism by which IR is known, but the effect of arsenic or folate deficiency remains unclear. Their effect may be mediated by epigenetic alterations, leading to miRNA expression changes, and this experiment examined this hypothesis
We used microarrays to detail the miRNA expression profiles of TK6 cells treated with 2 uM sodium arsenite for 6 days, folate-deficient media for 6 days, or 2.5 Gy IR exposure either acutely at 4 hours post exposure or long-term at 6 days post exposure, as well as requiste controls, all in biological triplicate.
Keywords: exposure differences
 
Overall design TK6, were cultured in standard RPMI 1640 (Invitrogen Inc., Gaithersburg, MD) or folate-deficient RPMI 1640 (Invitrogen). Growth media was supplemented with 10% fetal bovine serum (Invitrogen) and 1% penicillin-streptomycin; dialyzed fetal bovine serum (Invitrogen) was added to the folate-deficient medium in order to eliminate folic acid in the serum. For controls, folate-deficiency, arsenic exposure, and 6-day ?-IR exposure groups, 106 cells were diluted into 50ml of appropriate growth media. For the 4-hour post-?-IR exposure group, 107 cells were diluted into 50ml of growth media. For the arsenic exposed group, sodium arsenite was added to the media to a concentration of 2 ?M. For the ?-IR exposure groups, cells were diluted and allowed to incubate for 4 hours prior to irradiation treatment, and were exposed at a dose rate of 86.76 rad/min to a final dose of 2.5 Gy using a Philips MGC-40 X-ray source. Following exposure, cells were returned to the incubator. After fours hours, the short-term post-??-IR exposure group was collected for RNA isolation, as well as a mock (control) group. All experimental and control conditions were performed in triplicate. For all other groups, cells were cultured for 6 days, with the media changed and renewed, with the appropriate treatment, on day 3.
 
Contributor(s) Marsit CJ, Eddy K, Kelsey KT
Citation(s) 17108120
Submission date Oct 12, 2006
Last update date Mar 16, 2012
Contact name Carmen J Marsit
E-mail(s) cmarsit@hsph.harvard.edu
Organization name Harvard School of Public Health
Department Genetics and Complex Diseases
Lab Kelsey
Street address 665 Huntington Avenue
City Boston
State/province MA
ZIP/Postal code 02115
Country USA
 
Platforms (1)
GPL4411 Ambion Human_Mouse_Rat mirVANA miRNA Bioarray_1566V1
Samples (21)
GSM139803 As treatment, biological rep1
GSM139804 As treatment, biological rep2
GSM139805 IR treatment 4h timepoint, biological rep2
Relations
BioProject PRJNA97827

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Supplementary file Size Download File type/resource
GSE6020_RAW.tar 730.0 Kb (http)(custom) TAR (of GPR)

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