Selectively targeting FLT3-ITD mutants over FLT3-wt by a novel inhibitor for acute myeloid leukemia

Haematologica. 2021 Feb 1;106(2):605-609. doi: 10.3324/haematol.2019.244186.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Humans
  • Leukemia, Myeloid, Acute* / drug therapy
  • Leukemia, Myeloid, Acute* / genetics
  • Mutation
  • Tandem Repeat Sequences / genetics
  • fms-Like Tyrosine Kinase 3 / genetics

Substances

  • FLT3 protein, human
  • fms-Like Tyrosine Kinase 3

Grants and funding

Funding: this work was supported by the National Natural Science Foundation of China (grant ns. 81773777, 81803366, 81872745, 81872748, 81673469), the “Personalized Medicines- Molecular Signature-Based Drug Discovery and Development”, Strategic Priority Research Program of the Chinese Academy of Sciences (grant n. XDA12020114), the National Science & Technology Major Project “Key New Drug Creation and Manufacturing Program” of China (grant n. 2018ZX09711002), the China Postdoctoral Science Foundation (grant ns. 2018T110634, 2018M630720, 2019M652057), the Postdoctoral Science Foundation of Anhui Province (grant ns. 2018B279, 2019B300, 2019B326), the Frontier Science Key Research Program of CAS (grant n. QYZDB-SSW-SLH037), the CASHIPS Director's Fund (grant n. BJPY2019A03), and the Key Program of 13th five-year plan of CASHIPS (grant n. KP-2017-26).