Emerging Roles of Protein S-Nitrosylation in Macrophages and Cancer Cells

被引:19
作者
Benhar, Moran [1 ]
机构
[1] Technion Israel Inst Technol, Rappaport Inst Res Med Sci, Dept Biochem, Fac Med, IL-31096 Haifa, Israel
基金
以色列科学基金会;
关键词
S-nitrosylation; macrophage; cancer; inflammation; thioredoxin; glutathione; proteomics; NF-KAPPA-B; NITRIC-OXIDE SYNTHASE; BIOTIN-SWITCH ASSAY; DEPENDENT GENE-TRANSCRIPTION; THIOREDOXIN REDUCTASE 1; NLRP3; INFLAMMASOME; PROSTATE-CANCER; BREAST-CANCER; MURINE MACROPHAGES; ESTROGEN-RECEPTOR;
D O I
10.2174/0929867323666160627114839
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Despite long and intensive investigation, the mechanisms by which nitric oxide (NO) regulates immune function and carcinogenesis remain incompletely understood. Protein S-nitrosylation, the covalent attachment of a nitroso group to a cysteine thiol, has emerged as a central mechanism of NO-dependent cellular regulation. In particular, recent research has revealed important roles for S-nitrosylation/denitrosylation in modulating the activity of macrophage and tumor cell proteins, implicating S-nitrosylation in the regulation of macrophage function as well as in tumor development and response to therapy. This review summarizes recent progress in the identification and characterization of S-nitrosylated proteins in macrophages and cancer cells. The review highlights key findings and insights obtained from functional and proteomic studies about the roles of S-nitrosylation in signaling, transcription, apoptosis and other cellular processes relevant to macrophage function and cancer progression. Some of the implications of recent discoveries for the development of novel anticancer approaches are also discussed.
引用
收藏
页码:2602 / 2617
页数:16
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