| Literature DB >> 32536235 |
Cong Liang1, Chun-Jin Peng1, Li-Na Wang1, Yu Li1, Li-Min Zheng1, Zhong Fan1, Dan-Ping Huang1, Wen-Yan Tang1, Xiao-Li Zhang1, Li-Bin Huang1, Yan-Lai Tang1, Xue-Qun Luo1.
Abstract
The prognosis of patients with acute myeloid leukemia (AML) caused by the FLT3-ITD mutation is poor. Arsenic trioxide (ATO) and all-trans retinoic acid (ATRA) can down-regulate FLT3-ITD level and selectively kill leukemia cells carrying the FLT3-ITD mutation. However, the mechanisms of action of these two compounds are unknown. Here, we found that ATO could bind FLT3-ITD at Lys91 and Asp225, whereas ATRA could bind FLT3-ITD at Lys5 and Gln6. Both compounds could not bind wild-type FLT3. Further studies revealed that ATO/ATRA may suppress the Expression of FLT3-ITD by promoting the UBE2L6-mediated ubiquitination pathway and decreasing the expression of C-MYC. However, further studies are needed to define the mechanisms of these compounds on AML. Our research provides an experimental basis for the use of ATO/ATRA in FLT3-ITD AML in clinical practice.Entities:
Keywords: Degradation; FLT3-ITD; acute myeloid leukemia; all-trans-retinoic acid; arsenic trioxide
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Year: 2020 PMID: 32536235 DOI: 10.1080/10428194.2020.1775212
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022