Anemia: progress in molecular mechanisms and therapies

被引:211
作者
Sankaran, Vijay G. [1 ,2 ,3 ]
Weiss, Mitchell J. [4 ]
机构
[1] Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Hematol & Oncol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
[3] Broad Inst Massachusetts Inst Technol & Harvard, Cambridge, MA USA
[4] St Jude Childrens Res Hosp, Dept Hematol, Memphis, TN 38105 USA
基金
美国国家卫生研究院;
关键词
SICKLE-CELL-DISEASE; FETAL-HEMOGLOBIN EXPRESSION; CONGENITAL ERYTHROPOIETIC PORPHYRIA; GENOME-WIDE ASSOCIATION; CHRONIC KIDNEY-DISEASE; ZINC-FINGER NUCLEASES; FACTOR KLF1 CAUSES; FREE ALPHA-GLOBIN; GENE-THERAPY; BETA-THALASSEMIA;
D O I
10.1038/nm.3814
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
Anemia is a major source of morbidity and mortality worldwide. Here we review recent insights into how red blood cells (RBCs) are produced, the pathogenic mechanisms underlying various forms of anemia, and novel therapies derived from these findings. It is likely that these new insights, mainly arising from basic scientific studies, will contribute immensely to both the understanding of frequently debilitating forms of anemia and the ability to treat affected patients. Major worldwide diseases that are likely to benefit from new advances include the hemoglobinopathies (beta-thalassemia and sickle cell disease); rare genetic disorders of RBC production; and anemias associated with chronic kidney disease, inflammation, and cancer. Promising new approaches to treatment include drugs that target recently defined pathways in RBC production, iron metabolism, and fetal globin-family gene expression, as well as gene therapies that use improved viral vectors and newly developed genome editing technologies.
引用
收藏
页码:221 / 230
页数:10
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