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A series of novel aryl-methanone derivatives as inhibitors of FMS-like tyrosine kinase 3 (FLT3) in FLT3-ITD-positive acute myeloid leukemia.
Author: BeyerMandy, BöhmerFrank D, DoveStefan, ElzSigurd, FiebigHeinz-Herbert, HenningerSven Julian, KlaegerSusan, KrämerOliver H, KusterBernhard, MahboobiSiavosh, PilslBernadette, PolzerHarald, PongratzHerwig, SellmerAndreas, SpiekermannKarsten, WirthLukas
Original Abstract of the Article :
Mutants of the FLT3 receptor tyrosine kinase (RTK) with duplications in the juxtamembrane domain (FLT3-ITD) act as drivers of acute myeloid leukemia (AML). Potent tyrosine kinase inhibitors (TKi) of FLT3-ITD entered clinical trials and showed a promising, but transient success due to the occurrence ...See full text at original site
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引用元:
https://doi.org/10.1016/j.ejmech.2020.112232
データ提供:米国国立医学図書館(NLM)
Targeting FLT3-ITD: A New Approach to Treating Acute Myeloid Leukemia
Acute myeloid leukemia (AML), a type of blood cancer characterized by the rapid proliferation of abnormal white blood cells, is a formidable foe, like a raging desert fire. This research, like a skilled firefighter seeking to extinguish this deadly blaze, explores the potential of targeting FLT3-ITD, a specific mutation in the FLT3 receptor tyrosine kinase, as a therapeutic strategy for AML. The study focuses on developing novel inhibitors of FLT3-ITD, aiming to effectively target this crucial driver of AML.
A Targeted Attack
The study, like a well-aimed arrow, identifies several novel aryl-methanone derivatives that demonstrate potent inhibition of FLT3-ITD. These compounds, like a carefully crafted weapon, effectively block the activity of FLT3-ITD, preventing the uncontrolled growth of leukemia cells. The research highlights the potential of these novel inhibitors to provide a new therapeutic option for patients with FLT3-ITD-positive AML. This research, like a strategic maneuver in a complex battle, offers a promising approach to combating this deadly disease.
Hope for a Brighter Future
This research offers a ray of hope for patients with FLT3-ITD-positive AML. It suggests that targeting FLT3-ITD with novel inhibitors like the aryl-methanone derivatives may provide a more effective and less toxic treatment option. This research, like a desert oasis providing relief from the scorching heat, offers a much-needed source of hope for those facing this challenging disease.
Dr. Camel's Conclusion
This research, like a caravan traversing a treacherous desert, explores the potential of novel aryl-methanone derivatives to target FLT3-ITD, a specific mutation driving acute myeloid leukemia. The findings suggest that these compounds may offer a more effective and less toxic treatment option, bringing hope to patients battling this challenging disease. It's a testament to the power of scientific innovation in the ongoing fight against cancer.
Date :
- Date Completed 2020-11-30
- Date Revised 2020-11-30
Further Info :
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