BMPs and their clinical potentials

被引:77
作者
Kim, Meejung [1 ]
Choe, Senyon [1 ,2 ]
机构
[1] Gachon Univ Med & Sci, Joint Ctr Biosci, Lee Gil Ya Canc & Diabet Res Inst, Inchon 406840, South Korea
[2] Salk Inst Biol Studies, Struct Biol Lab, La Jolla, CA 92037 USA
关键词
BMP; Cancer; Diabetes; Obesity; Pulmonary hypertension; TGF-beta; BONE MORPHOGENETIC PROTEINS; HEREDITARY HEMORRHAGIC TELANGIECTASIA; BROWN ADIPOSE-TISSUE; EPITHELIAL-MESENCHYMAL TRANSITION; HUMAN BREAST-CANCER; MATRIX GLA PROTEIN; PRIMARY PULMONARY-HYPERTENSION; ANTI-ANGIOGENIC THERAPY; PLURIPOTENT STEM-CELLS; BLOOD-VESSEL FORMATION;
D O I
10.5483/BMBRep.2011.44.10.619
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
Bone morphogenetic protein (BMP) signaling in diseases is the subject of an overwhelming array of studies. BMPs are excellent targets for treatment of various clinical disorders. Several BMPs have already been shown to be clinically beneficial in the treatment of a variety of conditions, including BMP-2 and BMP-7 that have been approved for clinical application in nonunion bone fractures and spinal fusions. With the use of BMPs increasingly accepted in spinal fusion surgeries, other therapeutic approaches targeting BMP signaling are emerging beyond applications to skeletal disorders. These approaches can further utilize next-generation therapeutic tools such as engineered BMPs and ex vivo-conditioned cell therapies. In this review, we focused to provide insights into such clinical potentials of BMPs in metabolic and vascular diseases, and in cancer. [BMB reports 2011; 44(10): 619-634]
引用
收藏
页码:619 / 634
页数:16
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