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Published on: July 20, 2019
S-Nitrosylation in Tumor Microenvironment
Vandana Sharma1, Veani Fernando1, Joshua Letson1
1Department of Cancer Biology, University of Toledo Health Science Campus, 3000 Arlington Ave., Toledo, OH 43614, USA.
Abstract:
S-nitrosylation is a selective and reversible post-translational modification of protein thiols by nitric oxide (NO), which is a bioactive signaling molecule, to exert a variety of effects. These effects include the modulation of protein conformation, activity, stability, and protein-protein interactions. S-nitrosylation plays a central role in propagating NO signals within a cell, tissue, and tissue microenvironment, as the nitrosyl moiety can rapidly be transferred from one protein to another upon contact. This modification has also been reported to confer either tumor-suppressing or tumor-promoting effects and is portrayed as a process involved in every stage of cancer progression. In particular, S-nitrosylation has recently been found as an essential regulator of the tumor microenvironment (TME), the environment around a tumor governing the disease pathogenesis. This review aims to outline the effects of S-nitrosylation on different resident cells in the TME and the diverse outcomes in a context-dependent manner. Furthermore, we will discuss the therapeutic potentials of modulating S-nitrosylation levels in tumors.
Insights
S-nitrosylation, a modification by nitric oxide (NO), impacts protein function and cellular signaling. This review explores its role in the tumor microenvironment (TME) and potential cancer therapies.
Area of Science:
- Biochemistry
- Molecular Biology
- Cancer Biology
Background:
- S-nitrosylation is a reversible post-translational modification of protein thiols by nitric oxide (NO).
- It modulates protein conformation, activity, stability, and interactions, propagating NO signals.
- S-nitrosylation influences both tumor suppression and promotion, impacting cancer progression.
Purpose of the Study:
- To review the effects of S-nitrosylation on cells within the tumor microenvironment (TME).
- To discuss the context-dependent outcomes of S-nitrosylation in the TME.
- To explore therapeutic strategies targeting S-nitrosylation in cancer.
Main Methods:
- Literature review of S-nitrosylation in cancer biology.
- Analysis of S-nitrosylation's role in tumor microenvironment regulation.
- Examination of therapeutic interventions modulating S-nitrosylation.
Main Results:
- S-nitrosylation is a key regulator of the TME.
- Its effects on TME cells are diverse and context-dependent.
- Modulating S-nitrosylation shows therapeutic potential in cancer treatment.
Conclusions:
- S-nitrosylation significantly impacts the TME and cancer pathogenesis.
- Targeting S-nitrosylation offers promising avenues for cancer therapy.
- Further research is needed to fully elucidate context-dependent effects for optimized treatment.
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