TY - JOUR
T1 - The emerging role of selenium metabolic pathways in cancer
T2 - New therapeutic targets for cancer
AU - Kalimuthu, Kalishwaralal
AU - Keerthana, Chenicheri K.
AU - Mohan, Manikandan
AU - Arivalagan, Jaison
AU - Christyraj, Johnson Retnaraj Samuel Selvan
AU - Firer, Michael A.
AU - Choudry, Mohammad Haroon Asif
AU - Anto, Ruby John
AU - Lee, Yong J.
N1 - Publisher Copyright:
© 2021 Wiley Periodicals LLC
PY - 2022/3
Y1 - 2022/3
N2 - Selenium (Se) is incorporated into the body via the selenocysteine (Sec) biosynthesis pathway, which is critical in the synthesis of selenoproteins, such as glutathione peroxidases and thioredoxin reductases. Selenoproteins, which play a key role in several biological processes, including ferroptosis, drug resistance, endoplasmic reticulum stress, and epigenetic processes, are guided by Se uptake. In this review, we critically analyze the molecular mechanisms of Se metabolism and its potential as a therapeutic target for cancer. Sec insertion sequence binding protein 2 (SECISBP2), which is a positive regulator for the expression of selenoproteins, would be a novel prognostic predictor and an alternate target for cancer. We highlight strategies that attempt to develop a novel Se metabolism-based approach to uncover a new metabolic drug target for cancer therapy. Moreover, we expect extensive clinical use of SECISBP2 as a specific biomarker in cancer therapy in the near future. Of note, scientists face additional challenges in conducting successful research, including investigations on anticancer peptides to target SECISBP2 intracellular protein.
AB - Selenium (Se) is incorporated into the body via the selenocysteine (Sec) biosynthesis pathway, which is critical in the synthesis of selenoproteins, such as glutathione peroxidases and thioredoxin reductases. Selenoproteins, which play a key role in several biological processes, including ferroptosis, drug resistance, endoplasmic reticulum stress, and epigenetic processes, are guided by Se uptake. In this review, we critically analyze the molecular mechanisms of Se metabolism and its potential as a therapeutic target for cancer. Sec insertion sequence binding protein 2 (SECISBP2), which is a positive regulator for the expression of selenoproteins, would be a novel prognostic predictor and an alternate target for cancer. We highlight strategies that attempt to develop a novel Se metabolism-based approach to uncover a new metabolic drug target for cancer therapy. Moreover, we expect extensive clinical use of SECISBP2 as a specific biomarker in cancer therapy in the near future. Of note, scientists face additional challenges in conducting successful research, including investigations on anticancer peptides to target SECISBP2 intracellular protein.
KW - cancer therapy
KW - glutathione peroxidase-4
KW - selenocysteine
KW - selenocysteine insertion sequence binding protein 2
KW - thioredoxin reductase 1
UR - http://www.scopus.com/inward/record.url?scp=85121482109&partnerID=8YFLogxK
U2 - 10.1002/jcb.30196
DO - 10.1002/jcb.30196
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AN - SCOPUS:85121482109
SN - 0730-2312
VL - 123
SP - 532
EP - 542
JO - Journal of Cellular Biochemistry
JF - Journal of Cellular Biochemistry
IS - 3
ER -