TY - JOUR
T1 - Glutamate in cancers
T2 - from metabolism to signaling
AU - Yi, Haowei
AU - Talmon, Geoff
AU - Wang, Jing
N1 - Funding Information:
This work was supported by NIH/NCI R01CA140988-01 to JW and partially supported by Chinese Scholar Council to HY.
Publisher Copyright:
© 2020. by the Journal of Biomedical Research.
PY - 2020
Y1 - 2020
N2 - Glutamine and glutamate are major bioenergy substrates for normal and cancer cell growth. Cancer cells need more biofuel than normal tissues for energy supply, anti-oxidation activity and biomass production. Genes related to metabolic chains in many cancers are somehow mutated, which makes cancer cells more glutamate dependent. Meanwhile, glutamate is an excitatory neurotransmitter for conducting signals through binding with different types of receptors in central neuron system. Interestingly, increasing evidences have shown involvement of glutamate signaling, guided through their receptors, in human malignancy. Dysregulation of glutamate transporters, such as excitatory amino acid transporter and cystine/glutamate antiporter system, also generates excessive extracellular glutamate, which in turn, activates glutamate receptors on cancer cells and results in malignant growth. These features make glutamate an attractive target for anti-cancer drug development with some glutamate targeted but blood brain barrier impermeable anti-psychosis drugs under consideration. We discussed the relevant progressions and drawbacks in this field herein.
AB - Glutamine and glutamate are major bioenergy substrates for normal and cancer cell growth. Cancer cells need more biofuel than normal tissues for energy supply, anti-oxidation activity and biomass production. Genes related to metabolic chains in many cancers are somehow mutated, which makes cancer cells more glutamate dependent. Meanwhile, glutamate is an excitatory neurotransmitter for conducting signals through binding with different types of receptors in central neuron system. Interestingly, increasing evidences have shown involvement of glutamate signaling, guided through their receptors, in human malignancy. Dysregulation of glutamate transporters, such as excitatory amino acid transporter and cystine/glutamate antiporter system, also generates excessive extracellular glutamate, which in turn, activates glutamate receptors on cancer cells and results in malignant growth. These features make glutamate an attractive target for anti-cancer drug development with some glutamate targeted but blood brain barrier impermeable anti-psychosis drugs under consideration. We discussed the relevant progressions and drawbacks in this field herein.
KW - cancers
KW - glutamate
KW - glutamate receptors
KW - glutamate transporters
KW - metabolism
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U2 - 10.7555/JBR.34.20190037
DO - 10.7555/JBR.34.20190037
M3 - Article
C2 - 32594024
AN - SCOPUS:85117212727
SN - 1674-8301
VL - 34
SP - 260
EP - 270
JO - Journal of Biomedical Research
JF - Journal of Biomedical Research
IS - 4
ER -