谷氨酰胺
化学
丙氨酸
丝氨酸
运输机
癌症研究
半胱氨酸
癌细胞
细胞生物学
癌症
生物化学
生物
氨基酸
基因
遗传学
酶
作者
Hongli Jiang,Ning Zhang,Tongzhong Tang,Feng Feng,Haopeng Sun,Wei Qu
标识
DOI:10.1016/j.phrs.2020.104844
摘要
Glutamine metabolism, described as major energy and building blocks supply to cell growth, has gained great attention. Alanine-Serine-Cysteine Transporter (ASCT2), which belongs to solute carried (SLC) family transporters and is encoded by the SLC1A5 gene serves as a significant role for glutamine transport. Indeed, ASCT2 is often overexpressed in highly proliferative cancer cells to fulfill enhanced glutamine demand. So far, ASCT2 has been proved to be a significant target during the carcinogenesis process, and emerging evidence reveals that ASCT2 inhibitors can provide a benefit strategy for cancer therapy. Herein, we describe the structure of ASCT2, and summarize its related regulatory factors which are associated with antitumor activity. Moreover, this review article highlights the remarkable reform of discovery and development for ASCT2 inhibitors. On the basis of case studies, our perspectives for targeting ASCT2 and development of ASCT2 antagonist are discussed in the final part.
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