Amino Acid Transporters as Targets for Cancer Therapy: Why, Where, When, and How

被引:81
作者
Broer, Stefan [1 ]
机构
[1] Australian Natl Univ, Res Sch Biol, Canberra, ACT 2600, Australia
基金
澳大利亚研究理事会;
关键词
LAT1; ASCT2; xCT; SNAT1; SNAT2; mTOR; GCN2; solute carrier; GLUTAMINE TRANSPORTER; GLYCINE TRANSPORTER; SELECTIVE INHIBITOR; CELLULAR-METABOLISM; POTENT INHIBITORS; ESSENTIAL GENES; TUMOR-GROWTH; DRUG TARGET; IN-VIVO; ASCT2;
D O I
10.3390/ijms21176156
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
Amino acids are indispensable for the growth of cancer cells. This includes essential amino acids, the carbon skeleton of which cannot be synthesized, and conditionally essential amino acids, for which the metabolic demands exceed the capacity to synthesize them. Moreover, amino acids are important signaling molecules regulating metabolic pathways, protein translation, autophagy, defense against reactive oxygen species, and many other functions. Blocking uptake of amino acids into cancer cells is therefore a viable strategy to reduce growth. A number of studies have used genome-wide silencing or knock-out approaches, which cover all known amino acid transporters in a large variety of cancer cell lines. In this review, these studies are interrogated together with other databases to identify vulnerabilities with regard to amino acid transport. Several themes emerge, such as synthetic lethality, reduced redundancy, and selective vulnerability, which can be exploited to stop cancer cell growth.
引用
收藏
页码:1 / 20
页数:20
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