Cystine transporter SLC7A11/xCT in cancer: ferroptosis, nutrient dependency, and cancer therapy

P Koppula, L Zhuang, B Gan - Protein & cell, 2021 - academic.oup.com
… , most cancer cells largely depend on the cystine transporter system x c − to import cystine, …
We will focus on SLC7A11 and refer to this cystine transporter as SLC7A11 throughout this …

The x cystine/glutamate antiporter: A potential target for therapy of cancer and other diseases

M Lo, YZ Wang, PW Gout - Journal of cellular physiology, 2008 - Wiley Online Library
transporter for cystine and glutamate, and its role in various diseases, particularly cancer. …
as sulfasalazine may prove useful in clinical cancer therapy, particularly in combination with …

Cystine‐glutamate antiporter xCT as a therapeutic target for cancer

L Liu, R Liu, Y Liu, G Li, Q Chen… - Cell biochemistry and …, 2021 - Wiley Online Library
transporter, which is electrically neutral and non-Na + dependent. Under physiological
conditions, extracellular cystine is … , is synthesized by rapidly reducing cystine into cysteine (Cys) …

[HTML][HTML] Cysteine transporter SLC3A1 promotes breast cancer tumorigenesis

Y Jiang, Y Cao, Y Wang, W Li, X Liu, Y Lv, X Li, J Mi - Theranostics, 2017 - ncbi.nlm.nih.gov
… of breast cancer cells, and determines breast cancer cell response to antioxidant N-acetylcysteine.
Thus, SLC3A1 can serve as a potential target for breast cancer therapy. …

Sulfasalazine‐induced cystine starvation: Potential use for prostate cancer therapy

DW Doxsee, PW Gout, T Kurita, M Lo, AR Buckley… - The …, 2007 - Wiley Online Library
… ), a potent inhibitor of the xc À cystine transporter. … therapy of a variety of cancers [2,3]. It is
based on inhibition of uptake of extracellular cystine (or the reduced form, cysteine) by cancers

[HTML][HTML] Cysteine metabolic circuitries: druggable targets in cancer

VDB Bonifácio, SA Pereira, J Serpa… - British journal of cancer, 2021 - nature.com
… or alkylating drugs used in cancer therapy, affording an important … transporter (RBAT,
also designated by SLC3A1) is another cystine transporter with possible implications in cancer

[HTML][HTML] Disulfidptosis: a new target for metabolic cancer therapy

P Zheng, C Zhou, Y Ding, S Duan - … of Experimental & Clinical Cancer …, 2023 - Springer
therapy using glucose transporter (GLUT) inhibitors can trigger disulfidptosis and inhibit
cancer … and high expression in kidney cancer cells mediates high rates of cystine uptake. The …

Cystine transporter regulation of pentose phosphate pathway dependency and disulfide stress exposes a targetable metabolic vulnerability in cancer

X Liu, K Olszewski, Y Zhang, EW Lim, J Shi… - Nature cell …, 2020 - nature.com
… cells can provide insights for targeting metabolic vulnerabilities in cancer therapies. One
notable example is the use of asparaginase to treat acute lymphoblastic leukaemia. Unlike …

[HTML][HTML] Amino acid transporters as targets for cancer therapy: why, where, when, and how

S Bröer - International journal of molecular sciences, 2020 - mdpi.com
… Cells can acquire either cysteine or cystine (Cys-SS-Cys) for incorporation into GSH. The …
cystine to cysteine. Accordingly, one of the targets of sulfasalazine is the cystine transporter xCT…

The amino acid transporter SLC7A11-mediated crosstalk implicated in cancer therapy and the tumor microenvironment

J He, X Wang, K Chen, M Zhang, J Wang - Biochemical pharmacology, 2022 - Elsevier
… Tumor cells rely mainly on the nutrient transporter protein SLC7A11 to obtain cystine from
extrinsic pathway and then reduce it to cysteine by consuming reduced nicotinamide adenine …