TY - JOUR A1 - Mora, Javier A1 - Mertens, Christina A1 - Meier, Julia K. A1 - Fuhrmann, Dominik Christian A1 - BrĂ¼ne, Bernhard A1 - Jung, Michaela T1 - Strategies to interfere with tumor metabolism through the interplay of innate and adaptive immunity T2 - Cells N2 - The inflammatory tumor microenvironment is an important regulator of carcinogenesis. Tumor-infiltrating immune cells promote each step of tumor development, exerting crucial functions from initiation, early neovascularization, to metastasis. During tumor outgrowth, tumor-associated immune cells, including myeloid cells and lymphocytes, acquire a tumor-supportive, anti-inflammatory phenotype due to their interaction with tumor cells. Microenvironmental cues such as inflammation and hypoxia are mainly responsible for creating a tumor-supportive niche. Moreover, it is becoming apparent that the availability of iron within the tumor not only affects tumor growth and survival, but also the polarization of infiltrating immune cells. The interaction of tumor cells and infiltrating immune cells is multifaceted and complex, finally leading to different activation phenotypes of infiltrating immune cells regarding their functional heterogeneity and plasticity. In recent years, it was discovered that these phenotypes are mainly implicated in defining tumor outcome. Here, we discuss the role of the metabolic activation of both tumor cells and infiltrating immune cells in order to adapt their metabolism during tumor growth. Additionally, we address the role of iron availability and the hypoxic conditioning of the tumor with regard to tumor growth and we describe the relevance of therapeutic strategies to target such metabolic characteristics. KW - tumor-associated macrophages KW - T cells KW - hypoxia KW - cancer cell metabolism KW - iron metabolism KW - iron chelator Y1 - 2019 UR - http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/50317 UR - https://nbn-resolving.org/urn:nbn:de:hebis:30:3-503177 SN - 2073-4409 N1 - This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0). VL - 8 IS - 5, Art. 445 SP - 1 EP - 20 PB - MDPI CY - Basel ER -