Cargando…
SIRT1 deacetylase promotes acquisition of genetic mutations for drug resistance in CML cells
BCR-ABL transforms bone marrow progenitor cells and promotes genome instability, leading to development of chronic myelogenous leukemia (CML). The tyrosine kinase inhibitor imatinib effectively treats CML, but acquired resistance can develop due to BCR-ABL mutations. Mechanisms for acquisition of BC...
Autores principales: | Wang, Zhiqiang, Yuan, Hongfeng, Roth, Mendel, Stark, Jeremy M., Bhatia, Ravi, Chen, WenYong |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3376246/ https://www.ncbi.nlm.nih.gov/pubmed/22410779 http://dx.doi.org/10.1038/onc.2012.83 |
Ejemplares similares
-
ATRA-Induced Cellular Differentiation and CD38 Expression Inhibits Acquisition of BCR-ABL Mutations for CML Acquired Resistance
por: Wang, Zhiqiang, et al.
Publicado: (2014) -
SIRT1 and LSD1 competitively regulate KU70 functions in DNA repair and mutation acquisition in cancer cells
por: Roth, Mendel, et al.
Publicado: (2016) -
Metabolic alterations mediated by STAT3 promotes drug persistence in CML
por: Patel, Sweta B., et al.
Publicado: (2021) -
An inactivating mutation in the histone deacetylase SIRT6 causes human perinatal lethality
por: Ferrer, Christina M., et al.
Publicado: (2018) -
Depletion of γ-catenin by Histone Deacetylase Inhibition Confers Elimination of CML Stem Cells in Combination with Imatinib
por: Jin, Yanli, et al.
Publicado: (2016)