| Literature DB >> 25258669 |
Jianbiao Zhou1, Wee-Joo Chng1.
Abstract
Accumulating evidence support the notion that acute myeloid leukemia (AML) is organized in a hierarchical system, originating from a special proportion of leukemia stem cells (LSC). Similar to their normal counterpart, hematopoietic stem cells (HSC), LSC possess self-renewal capacity and are responsible for the continued growth and proliferation of the bulk of leukemia cells in the blood and bone marrow. It is believed that LSC are also the root cause for the treatment failure and relapse of AML because LSC are often resistant to chemotherapy. In the past decade, we have made significant advancement in identification and understanding the molecular biology of LSC, but it remains a daunting task to specifically targeting LSC, while sparing normal HSC. In this review, we will first provide a historical overview of the discovery of LSC, followed by a summary of identification and separation of LSC by either cell surface markers or functional assays. Next, the review will focus on the current, various strategies for eradicating LSC. Finally, we will highlight future directions and challenges ahead of our ultimate goal for the cure of AML by targeting LSC.Entities:
Keywords: Acute myeloid leukemia; Cancer stem cell; Cell therapy; Immunotherapy; Leukemia stem cell
Year: 2014 PMID: 25258669 PMCID: PMC4172676 DOI: 10.4252/wjsc.v6.i4.473
Source DB: PubMed Journal: World J Stem Cells ISSN: 1948-0210 Impact factor: 5.326