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Status |
Public on Aug 17, 2021 |
Title |
ATAC-seq of lung cancer cell lines with doxycycline KRAS G12V and drug treatments |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
We modelled the effects of KRAS activation on three SCLC cell lines H2107, H82, H524 and investigated the effects of KRAS induction and various drug treatments on motif and chromatin accessibility profiles.
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Overall design |
H2107-KRAS G12V and H524-KRAS G12V cells treated with doxycycline ± SCH772984 (1 μM) for 72 hours. H82-KRASG12V cells were treated with the following chemicals: doxycycline; doxycycline + SCH772984 (1 μM); doxycycline + SB747651A (5 μM); doxycycline + A-485 (400 nM); or doxycycline + SB747651A (5 μM) + A-485 (400 nM). After 72 hours treatment, these cells as well as corresponding non-treated control cells were collected and frozen.
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Contributor(s) |
Inoue Y, Nikolic A, Liu A, Ladanyi M, Somwar R, Gallo M, Lockwood WW |
Citation(s) |
34121659 |
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Submission date |
Oct 27, 2020 |
Last update date |
Aug 18, 2021 |
Contact name |
Marco Gallo |
Organization name |
University of Calgary
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Department |
Biochemistry and Molecular Biology
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Lab |
Gallo lab
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Street address |
2500 University Dr NW
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City |
Calgary |
State/province |
AB |
ZIP/Postal code |
T2N 1N4 |
Country |
Canada |
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Platforms (1) |
GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
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Samples (36)
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Relations |
BioProject |
PRJNA672329 |
SRA |
SRP288770 |