D-serine accelerates gastric tumor growth by suppressing killer T cells

Researchers have discovered that D-serine, a metabolic byproduct, helps gastric cancer tumors evade the immune system by suppressing killer T cells. This finding suggests that D-serine levels could influence the effectiveness of immune checkpoint inhibitor therapies.
Why it matters
Understanding how tumors manipulate metabolic pathways is essential for developing more effective cancer immunotherapies and overcoming treatment resistance.
edited by Sadie Harley , reviewed by Robert Egan
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Add as preferred source D-serine is a metabolic byproduct that aids immune evasion by gastric cancer tumors. It increases immunosuppressive macrophage activity and reduces the numbers and function of cytotoxic T cells. This aids tumor growth and provides resistance against immune checkpoint inhibitor therapy. Credit: Keio University Global Research Institute (KGRI) One of the crucial steps in cancer proliferation is evading killer immune cells. Cancer cells use a variety of signaling molecules to evade the immune system. Immune checkpoint inhibitor (ICI) therapy interferes with some of these evasion tactics, improving the immune system's ability to suppress tumors. However, the success of ICI therapy depends on the specific signals being secreted by the tumor.
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