Literature DB >> 27581135

Induction of Chronic Myeloid Leukemia in Mice.

Haojian Zhang1, Shaoguang Li2.   

Abstract

Chronic myeloid leukemia (CML) is a myeloproliferative disorder derived from a hematopoietic stem cell (HSC), harboring Philadelphia chromosome (Ph chromosome). Formation of the Ph chromosome is caused by a reciprocal translocation between the chromosomes 9 and 22 t(9;22)(q34;q11), resulting in a fusion protein known as BCR-ABL which has constitutive tyrosine kinase activity and promotes the proliferation of leukemia cells via multiple mechanisms. Studies on CML have led to the identification of the first cancer-associated chromosomal abnormality and the subsequent development of tyrosine kinase inhibitors (TKIs) that inhibit BCR-ABL kinase activity in CML. It has become clear that leukemia stem cells (LSCs) in CML are insensitive to inhibition by TKIs, and eradication of LSCs appears to be difficult. Therefore, some of the major issues in current CML therapy are to understand the biology of LSCs and to investigate why LSCs are insensitive to TKIs for developing curative therapeutic strategies. In this regard, application of mouse models recapitulating human CML disease will be critical. In this chapter, we describe methods for induction of CML in mice with BCR-ABL.

Entities:  

Keywords:  BCR-ABL; Chronic myeloid leukemia; Mouse model; Philadelphia chromosome; Transduction; Transplantation

Mesh:

Substances:

Year:  2016        PMID: 27581135     DOI: 10.1007/978-1-4939-4011-0_2

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

1.  CRISPR/Cas9-Directed Gene Trap Constitutes a Selection System for Corrected BCR/ABL Leukemic Cells in CML.

Authors:  Elena Vuelta; José L Ordoñez; David J Sanz; Sandra Ballesteros; Jesús M Hernández-Rivas; Lucía Méndez-Sánchez; Manuel Sánchez-Martín; Ignacio García-Tuñón
Journal:  Int J Mol Sci       Date:  2022-06-07       Impact factor: 6.208

Review 2.  Preclinical approaches in chronic myeloid leukemia: from cells to systems.

Authors:  Cassie J Clarke; Tessa L Holyoake
Journal:  Exp Hematol       Date:  2016-12-23       Impact factor: 3.084

  2 in total

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