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Status |
Public on Dec 02, 2021 |
Title |
Targeted inhibition of LIFR enhances therapeutic efficacy of HDAC inhibitors in triple negative breast cancer |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Here, we examined the therapeutic utility of EC359 in improving the therapeutic efficacy of HDACi in TNBC models. BT-549 cells were treated with vehicle (DMSO), EC359, HDACi(Vorinostat), EC359+HDACi and the RNA was isolated and utilized for RNA-seq analysis. Our results demonstrated that the beneficial effect of the EC359+HDACi involves regulation of multiple genes that involved in several pathways including apoptosis, metabolism and cell cycle.
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Overall design |
Total RNA was isolated from BT-549 cells. Illumina TruSeq RNA Sample Preparation was performed following manufacturer's protocol. Samples were run on an Illumina HiSeq 3000 in duplicate. The combined raw reads were aligned to UCSC hg19 by Tophat. Genes were annotated and quantified by HTSeq-DESeq pipeline.
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Contributor(s) |
Viswanadhapalli S, Chen Y, Zou Y, Vadlamudi RK |
Citation(s) |
34716410 |
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Submission date |
Dec 15, 2020 |
Last update date |
Dec 03, 2021 |
Contact name |
YI ZOU |
E-mail(s) |
zou@uthscsa.edu
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Organization name |
UTHSA-GCCRI
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Street address |
8403 Floyd Curl Drive
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City |
SAN ANTONIO |
State/province |
TX |
ZIP/Postal code |
78229 |
Country |
USA |
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Platforms (1) |
GPL21290 |
Illumina HiSeq 3000 (Homo sapiens) |
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Samples (8)
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Relations |
BioProject |
PRJNA685420 |
SRA |
SRP298026 |