Enhancing cancer immunotherapy via inhibition of soluble epoxide hydrolase.
Abigail G KellyWeicang WangEva RothenbergerJun YangMolly M GilliganFranciele C KipperAhmed AttayaAllison GartungSung Hee HwangMichael J GillespieRachel L BayerKatherine M QuinlivanKimberly L TorresSui HuangNicholas MitsiadesHaixia YangBruce D HammockDipak PanigrahyPublished in: Proceedings of the National Academy of Sciences of the United States of America (2024)
Cancer therapy, including immunotherapy, is inherently limited by chronic inflammation-induced tumorigenesis and toxicity within the tumor microenvironment. Thus, stimulating the resolution of inflammation may enhance immunotherapy and improve the toxicity of immune checkpoint inhibition (ICI). As epoxy-fatty acids (EpFAs) are degraded by the enzyme soluble epoxide hydrolase (sEH), the inhibition of sEH increases endogenous EpFA levels to promote the resolution of cancer-associated inflammation. Here, we demonstrate that systemic treatment with ICI induces sEH expression in multiple murine cancer models. Dietary omega-3 polyunsaturated fatty acid supplementation and pharmacologic sEH inhibition, both alone and in combination, significantly enhance anti-tumor activity of ICI in these models. Notably, pharmacological abrogation of the sEH pathway alone or in combination with ICI counter-regulates an ICI-induced pro-inflammatory and pro-tumorigenic cytokine storm. Thus, modulating endogenous EpFA levels through dietary supplementation or sEH inhibition may represent a unique strategy to enhance the anti-tumor activity of paradigm cancer therapies.