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Status |
Public on May 30, 2024 |
Title |
BCAT1 contributes to the developmentproliferation and leukemogenesis of TKI-resistant CML |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
In this report, we revealed that branched chain amino acid transaminase 1 (BCAT1) is highly enriched in both mouse and human TKI-resistant CML cells. Leukemia was almost completely abrogated upon BCAT1 knockdown during transplantation in a BCR-ABLT315I-induced murine TKI-resistant CML model . Moreover, knockdown of BCAT1 led to a dramatic decrease in the proliferation of TKI-resistant human leukemia cell lines. BCAA/BCAT1 signaling enhanced the phosphorylation of CREB, which is required for maintenance of TKI-resistant CML cells. Importantly, blockade of BCAA/BCAT1 signaling efficiently inhibited leukemogenesis both in vivo and in vitro.
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Overall design |
We performed transcriptome sequencing (RNA-seq) using BCAT1-knockdown and Scramble 32Dcl3 cells
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Contributor(s) |
Jiang Y, Huang D |
Citation missing |
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Submission date |
Mar 25, 2024 |
Last update date |
May 30, 2024 |
Contact name |
yu Jiang |
E-mail(s) |
jiangyu1995@sjtu.edu.cn
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Phone |
+8615213086391
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Organization name |
Shanghai Jiao Tong University School of Medicine
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Department |
Faculty of Basic Medicine
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Lab |
Key Laboratory of Cell Differentiation and Apoptosis of Chinese Ministry of Education
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Street address |
280 Chongqing South Road, Shanghai
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City |
Shanghai |
ZIP/Postal code |
200025 |
Country |
China |
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Platforms (1) |
GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
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Samples (2) |
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Relations |
BioProject |
PRJNA1091685 |