Roles of SIRT1 in leukemogenesis

被引:33
|
作者
Chen, WenYong [1 ]
Bhatia, Ravi [2 ]
机构
[1] City Hope Natl Med Ctr, Beckman Res Inst, Dept Canc Biol, Duarte, CA 91010 USA
[2] City Hope Natl Med Ctr, Div Hematopoiet Stem Cell & Leukemia Res, Duarte, CA 91010 USA
基金
美国国家卫生研究院;
关键词
acquired resistance; BCR-ABL; chronic myeloid leukemia; leukemic stem cells; SIRT1; CHRONIC MYELOID-LEUKEMIA; CHRONIC MYELOGENOUS LEUKEMIA; DEPENDENT HISTONE DEACETYLASE; HEMATOPOIETIC STEM-CELLS; DOUBLE-STRAND BREAKS; GENE-EXPRESSION; TYROSINE KINASE; CANCER; IMATINIB; INHIBITION;
D O I
10.1097/MOH.0b013e328360ab64
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of reviewThis review provides a concise summary of significant research progress on SIRT1 deacetylase in leukemia in the past year. SIRT1 is a multifunctional protein and recent studies demonstrate that SIRT1 plays a crucial role in myeloid leukemogenesis and drug resistance.Recent findingsSIRT1 expression is typically low in normal adult hematopoietic stem/progenitor cells, but is increased in the leukemic stem/progenitor cells of chronic myeloid leukemia (CML). SIRT1 activation is mediated in both BCR-ABL tyrosine kinase-dependent and independent manners. SIRT1 activation promotes resistance of CML stem cells to tyrosine kinase inhibitors and acquisition of BCR-ABL mutations for acquired resistance.SummaryOn the basis of current findings, SIRT1 inhibition in combination with BCR-ABL tyrosine kinase inhibitors can be explored as a novel approach to eradicate leukemic stem cells and residual disease in chronic phase CML. SIRT1 inhibition may also help prevent acquired resistance through genetic mutations of advanced phases of CML, and extend remission.
引用
收藏
页码:308 / 313
页数:6
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