ABC transporters: human disease and pharmacotherapeutic potential

被引:23
|
作者
Moore, Jonathan M. [1 ]
Bell, Eric L. [1 ]
Hughes, Robert O. [1 ]
Garfield, Alastair S. [1 ]
机构
[1] Rectify Pharmaceut, Cambridge, MA 02139 USA
关键词
ATP-BINDING CASSETTE; X-LINKED ADRENOLEUKODYSTROPHY; SALT EXPORT PUMP; BILIARY CHOLESTEROL SECRETION; CYSTIC-FIBROSIS; MOUSE MODEL; INTRAHEPATIC CHOLESTASIS; PSEUDOXANTHOMA ELASTICUM; ALZHEIMERS-DISEASE; AMYLOID DEPOSITION;
D O I
10.1016/j.molmed.2022.11.001
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
Adenosine triphosphate (ATP)-binding cassette (ABC) transporters are a 48-member superfamily of membrane proteins that actively transport a variety of biological substrates across lipid membranes. Their functional diversity defines an expansive involvement in myriad aspects of human biology. At least 21 ABC transporters underlie rare monogenic disorders, with even more implicated in the predisposition to and symptomology of common and complex diseases. Such broad (patho)physiological relevance places this class of proteins at the intersection of disease causation and therapeutic potential, underlining them as promising targets for drug discovery, as exemplified by the transformative CFTR (ABCC7) modulator therapies for cystic fibrosis. This review will explore the growing relevance of ABC transporters to human disease and their potential as small-molecule drug targets.
引用
收藏
页码:152 / 172
页数:21
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