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Eicosanoids in Cancer: Prostaglandin E2 Receptor 4 in Cancer Therapeutics and Immunotherapy
Mc Millan Ching1, Jocelyn Reader2,3, Amy M Fulton3,4,5
1Cellular and Molecular Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Abstract:
The cyclooxygenase-2 (COX-2) enzyme is frequently overexpressed in epithelial malignancies including those of the breast, prostate, lung, kidney, ovary, and liver and elevated expression is associated with worse outcomes. COX-2 catalyzes the metabolism of arachidonic acid to prostaglandins. The COX-2 product prostaglandin E2 (PGE2) binds to four G-protein-coupled EP receptors designated EP1-EP4. EP4 is commonly upregulated in cancer and supports cell proliferation, migration, invasion, and metastasis through activation of multiple signaling pathways including ERK, cAMP/PKA, PI3K/AKT, and NF-κB. EP4 antagonists inhibit metastasis in preclinical models. Cancer stem cells, that underlie therapy resistance and disease relapse, are driven by the expression of EP4. Resistance to several chemotherapies is reversed in the presence of EP4 antagonists. In addition to tumor cell-autonomous roles of EP4, many EP4-positive host cells play a role in tumor behavior. Endothelial cell-EP4 supports tumor angiogenesis and lymphangiogenesis. Natural Killer (NK) cells are critical to the mechanism by which systemically administered EP4 antagonists inhibit metastasis. PGE2 acts on EP4 expressed on the NK cell to inhibit tumor target cell killing, cytokine production, and chemotactic activity. Myeloid-derived suppressor cells (MDSCs), that inhibit the development of cytotoxic T cells, are induced by PGE2 acting on myeloid-expressed EP2 and EP4 receptors. Inhibition of MDSC-EP4 leads to maturation of effector T cells and suppresses the induction of T regulatory cells. A number of EP4 antagonists have proven useful in dissecting these mechanisms. There is growing evidence that EP4 antagonism, particularly in combination with either chemotherapy, endocrine therapy, or immune-based therapies, should be investigated further as a promising novel approach to cancer therapy. Several EP4 antagonists have now progressed to early phase clinical trials and we eagerly await the results of those studies.
Insights
EP4 receptor antagonists show promise in cancer therapy by inhibiting tumor growth, metastasis, and therapy resistance. Targeting EP4 may overcome resistance and improve outcomes when combined with existing treatments.
Area of Science:
- Oncology
- Molecular Biology
- Immunology
Background:
- Cyclooxygenase-2 (COX-2) is overexpressed in many epithelial cancers, correlating with poor prognosis.
- COX-2 metabolizes arachidonic acid to prostaglandin E2 (PGE2), which signals through EP receptors.
- EP4 receptor is frequently upregulated in cancer, promoting tumor progression and metastasis.
Purpose of the Study:
- To investigate the role of EP4 receptor in cancer progression and therapeutic resistance.
- To evaluate the potential of EP4 antagonists as a novel cancer therapy strategy.
Main Methods:
- Preclinical models were used to assess the effects of EP4 antagonists on metastasis.
- Studies examined EP4's role in cancer stem cells, chemotherapy resistance, angiogenesis, and immune cell function (NK cells, MDSCs).
Main Results:
- EP4 antagonists inhibited metastasis in preclinical models.
- EP4 drives cancer stem cell function and chemotherapy resistance.
- EP4 on endothelial cells supports angiogenesis; EP4 on NK cells and MDSCs modulates anti-tumor immunity.
Conclusions:
- EP4 antagonism is a promising therapeutic strategy, particularly in combination with chemotherapy, endocrine therapy, or immunotherapy.
- Further clinical investigation of EP4 antagonists is warranted given their potential to overcome resistance and enhance treatment efficacy.
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