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Published on: June 12, 2021
O-GlcNAcylation at the center of antitumor immunity
Graham A Heieis1, Bart Everts1
1Department of Parasitology, Leiden University Medical Center, Albinusdreef 2, 2333 ZA Leiden, the Netherlands.
Abstract:
The post-translational modification known as O-GlcNAcylation is a highly dysregulated process in tumors, and a key contributor to malignant transformation. In contrast, after three decades since its discovery, very little has been revealed about this process in the immune system. With the prospect of targeting O-GlcNAcylation as tumor therapy, greater understanding of how it regulates immune responses in the context of the tumor microenvironment will be needed. Here, we discuss recent discoveries from which a picture is emerging that O-GlcNAcylation, in either tumors or in immune cells, could negatively impact overall antitumor immune responses. We propose that interference with O-GlcNAcylation thus holds promise for cancer treatment from both perspectives.
Insights
O-GlcNAcylation, a process dysregulated in tumors, negatively impacts antitumor immunity in both cancer cells and immune cells. Targeting this modification offers a promising strategy for novel cancer therapies.
Area of Science:
- Biochemistry
- Immunology
- Cancer Biology
Background:
- O-GlcNAcylation is a post-translational modification frequently dysregulated in cancer.
- Its role in the immune system, particularly within the tumor microenvironment, remains largely unexplored.
- Understanding O-GlcNAcylation's impact on immune responses is crucial for developing new cancer therapies.
Purpose of the Study:
- To review recent discoveries on O-GlcNAcylation in the context of tumors and the immune system.
- To elucidate the role of O-GlcNAcylation in regulating antitumor immune responses.
- To explore the therapeutic potential of targeting O-GlcNAcylation in cancer treatment.
Main Methods:
- Literature review and synthesis of recent findings.
- Analysis of O-GlcNAcylation's impact on tumor cells.
- Evaluation of O-GlcNAcylation's effects on immune cells within the tumor microenvironment.
Main Results:
- Emerging evidence suggests O-GlcNAcylation negatively impacts antitumor immunity.
- Dysregulated O-GlcNAcylation in tumors can impair anti-cancer immune responses.
- O-GlcNAcylation in immune cells also appears to suppress antitumor immunity.
Conclusions:
- O-GlcNAcylation plays a significant, often detrimental, role in antitumor immunity.
- Targeting O-GlcNAcylation in both cancer cells and immune cells presents a dual therapeutic strategy.
- Interference with O-GlcNAcylation holds promise for enhancing cancer treatment outcomes.
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