Inflammation is an important component of the tumor microenvironment. IL-1 is an inflammatory cytokine which plays a key role in carcinogenesis and tumor progression. IL-1 is subject to regulation by components of the IL-1 and IL-1 receptor (ILR) families. Negative regulators include a decoy receptor (IL-1R2), receptor antagonists (IL-1Ra), IL-1R8, and anti-inflammatory IL-37. IL-1 acts at different levels in tumor initiation and progression, including driving chronic non-resolving inflammation, tumor angiogenesis, activation of the IL-17 pathway, induction of myeloid-derived suppressor cells (MDSC) and macrophage recruitment, invasion and metastasis. Based on initial clinical results, the translation potential of IL-1 targeting deserves extensive analysis.
Domenico Supino, Sadaf Davoudian, Rita Silva-Gomes, Daniele Piovani, Rita Garuti, Antonio Desai, Sarah N. Mapelli, Francesco Scavello, Silvia Carnevale, Andrea Mariancini, Elena Magrini, Roberto Leone, Marina Sironi, Sonia Valentino, Diletta Di Mitri, Federica Portale, Carlo Mario Fedeli, D.P. Comina, Stefanos Bonovas, Antonio Voza, Alberto Mantovani, Barbara Bottazzi, Cecília Garlanda
Suzhao Li, C. Preston Neff, Kristina Barber, Jaewoo Hong, Yuchun Luo, Tania Azam, Brent E. Palmer, Mayumi Fujita, Cecília Garlanda, Alberto Mantovani, Soohyun Kim, Charles A. Dinarello
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