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Series GSE272312 Query DataSets for GSE272312
Status Public on Aug 31, 2024
Title Effect of abemaiclicb and deletion of TP53 on gene expression in MCF7 cells at different timepoints
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary CDK4/6 inhibitor, abemaciclib induced cell cycle arrest and senescence in breast cancer. We reported that deletion of TP53 prevented the senescence features. In this study, we knockout TP53 by CRISPR Cas9 system and treated MCF7 cells and p53 knockout cells with abemaciclib for up to 29 days to identify the difference of senescence associated secretary phenotype genes and cell cycle related genes. features.
 
Overall design We established TP53 knockout (p53KO) cell line by CRISPR Cas9 system in MCF7 breast cancer cell line. Cells were treated with 50 nM abemaciclib. We collected cells on day 0 (no treatment), day1, day 3, day 14 and day 21. We then performed gene expression profiling analysis from RNA sequencing of parental MCF7 and p53KO cell.
 
Contributor(s) Kudo R, Chandarlapaty S
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Submission date Jul 16, 2024
Last update date Aug 31, 2024
Contact name Rei Kudo
E-mail(s) reikudobc@gmail.com
Organization name Memorial Sloan Kettering Cancer Center
Department HOPP
Lab Chandarlapaty Lab
Street address 417 E 68th Street
City New York
State/province NY
ZIP/Postal code 10065
Country USA
 
Platforms (1)
GPL34281 Illumina NovaSeq X (Homo sapiens)
Samples (24)
GSM8398269 MCF7 parental, Day 0 rep 1
GSM8398270 MCF7 parental, Day 0 rep 2
GSM8398271 MCF7 parental, Day 0 rep 3
Relations
BioProject PRJNA1136408

Download family Format
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Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE272312_RAW.tar 104.2 Mb (http)(custom) TAR (of TXT)
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Raw data are available in SRA

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