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Buthionine sulfoximine and chemoresistance in cancer treatments: a systematic review with meta-analysis of preclinical studies

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TAYLOR & FRANCIS INC
DOI: 10.1080/10937404.2023.2246876

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Adjuvant treatment; buthionine sulfoximine; chemotherapy; glutathione; oxidative damage; >

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Buthionine sulfoximine (BSO) is a synthetic amino acid that inhibits the production of a cellular antioxidant called reduced glutathione (GSH), which is present in tumor cells. By depleting GSH, BSO enhances the cytotoxicity of chemotherapy drugs in drug-resistant tumors. A systematic review and meta-analysis of preclinical studies found that BSO alone exhibits cytotoxic activity and is commonly used in combination with other antineoplastic strategies to improve treatment efficacy. This review provides important considerations for the use of BSO in cancer treatment and highlights its potential as an adjuvant therapy.
Buthionine sulfoximine (BSO) is a synthetic amino acid that blocks the biosynthesis of reduced glutathione (GSH), an endogenous antioxidant cellular component present in tumor cells. GSH levels have been associated with tumor cell resistance to chemotherapeutic drugs and platinum compounds. Consequently, by depleting GSH, BSO enhances the cytotoxicity of chemotherapeutic agents in drug-resistant tumors. Therefore, the aim of this study was to conduct a systematic review with meta-analysis of preclinical studies utilizing BSO in cancer treatments. The systematic search was carried out using the following databases: PubMed, Web of Science, Scopus, and EMBASE up until March 20, 2023, in order to collect preclinical studies that evaluated BSO, alone or in association, as a strategy for antineoplastic therapy. One hundred nine investigations were found to assess the cytotoxic potential of BSO alone or in combination with other compounds. Twenty-one of these met the criteria for performing the meta-analysis. The evidence gathered indicated that BSO alone exhibits cytotoxic activity. However, this compound is generally used in combination with other antineoplastic strategies, mainly chemotherapy ones, to improve cytotoxicity to carcinogenic cells and treatment efficacy. Finally, this review provides important considerations regarding BSO use in cancer treatment conditions, which might optimize future studies as a potential adjuvant antineoplastic therapeutic tool.

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