Bone Marrow Microenvironment as a Source of New Drug Targets for the Treatment of Acute Myeloid Leukaemia

被引:12
|
作者
Skelding, Kathryn A. [1 ,2 ]
Barry, Daniel L. [1 ,2 ]
Theron, Danielle Z. [1 ,2 ]
Lincz, Lisa F. [2 ,3 ]
机构
[1] Univ Newcastle, Coll Hlth Med & Wellbeing, Sch Biomed Sci Pharm, Canc Cell Biol Res Grp, Callaghan, NSW 2308, Australia
[2] Hunter Med Res Inst, Precis Med Res Program, New Lambton Hts, NSW 2305, Australia
[3] Calvary Mater Newcastle Hosp, Hunter Hematol Res Grp, Waratah, NSW 2298, Australia
关键词
acute myeloid leukaemia; AML; bone marrow microenvironment; drug targets; bone marrow niche; HEMATOPOIETIC STEM-CELLS; HYPOXIA-ACTIVATED PRODRUG; ENDOTHELIAL GROWTH-FACTOR; CHEMOKINE RECEPTOR CXCR4; REGULATORY T-CELLS; NF-KAPPA-B; IN-VIVO; STROMAL CELLS; CELLULAR SENESCENCE; C-MYC;
D O I
10.3390/ijms24010563
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Acute myeloid leukaemia (AML) is a heterogeneous disease with one of the worst survival rates of all cancers. The bone marrow microenvironment is increasingly being recognised as an important mediator of AML chemoresistance and relapse, supporting leukaemia stem cell survival through interactions among stromal, haematopoietic progenitor and leukaemic cells. Traditional therapies targeting leukaemic cells have failed to improve long term survival rates, and as such, the bone marrow niche has become a promising new source of potential therapeutic targets, particularly for relapsed and refractory AML. This review briefly discusses the role of the bone marrow microenvironment in AML development and progression, and as a source of novel therapeutic targets for AML. The main focus of this review is on drugs that modulate/target this bone marrow microenvironment and have been examined in in vivo models or clinically.
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页数:39
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