| Literature DB >> 34935169 |
Kalishwaralal Kalimuthu1,2, Chenicheri K Keerthana2, Manikandan Mohan3,4, Jaison Arivalagan5, Johnson Retnaraj Samuel Selvan Christyraj6, Michael A Firer7,8,9, Mohammad Haroon Asif Choudry1, Ruby John Anto2, Yong J Lee1.
Abstract
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.Entities:
Keywords: cancer therapy; glutathione peroxidase-4; selenocysteine; selenocysteine insertion sequence binding protein 2; thioredoxin reductase 1
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Year: 2021 PMID: 34935169 PMCID: PMC8940641 DOI: 10.1002/jcb.30196
Source DB: PubMed Journal: J Cell Biochem ISSN: 0730-2312 Impact factor: 4.429