Comprehensive review of amino acid transporters as therapeutic targets

被引:5
|
作者
Xia, Ran [1 ]
Peng, Hai-Feng [1 ]
Zhang, Xing [1 ]
Zhang, Hong-Sheng [1 ]
机构
[1] Beijing Univ Technol, Coll Chem & Life Sci, Pingleyuan 100, Beijing 100124, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
SLC transporter; amino acid transporter; cancer therapy; targeted therapy; HIGH-AFFINITY GLUTAMATE; THREO-BETA-BENZYLOXYASPARTATE; FUNCTIONAL-CHARACTERIZATION; SELECTIVE INHIBITOR; GENE; METABOLISM; MECHANISM; PROTEIN; MUTATIONS; BINDING;
D O I
10.1016/j.ijbiomac.2024.129646
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
The solute carrier (SLC) family, with more than 400 membrane -bound proteins, facilitates the transport of a wide array of substrates such as nutrients, ions, metabolites, and drugs across biological membranes. Amino acid transporters (AATs) are membrane transport proteins that mediate transfer of amino acids into and out of cells or cellular organelles. AATs participate in many important physiological functions including nutrient supply, metabolic transformation, energy homeostasis, redox regulation, and neurological regulation. Several AATs have been found to significantly impact the progression of human malignancies, and dysregulation of AATs results in metabolic reprogramming affecting tumor growth and progression. However, current clinical therapies that directly target AATs have not been developed. The purpose of this review is to highlight the structural and functional diversity of AATs, the molecular mechanisms in human diseases such as tumors, kidney diseases, and emerging therapeutic strategies for targeting AATs.
引用
收藏
页数:21
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