TY - JOUR AB - Immune checkpoint inhibition and chimeric antigen receptor (CAR) T cell therapy have demonstrated stunning clinical efficacy in many cancer types. However, most patients do not respond to immunotherapies or relapse after an initial response, stressing the need for improved strategies. Chemokines, as mediators of immune cell trafficking, play an important role in the composition of the tumor microenvironment and exert both pro- and antitumorigenic functions. Here, chemokines may represent valuable prognostic biomarkers of response to immunotherapy and a strategy to improve immunotherapies. In this review, the pleiotropic functions of chemokines in the tumor microenvironment (TME) and strategies of utilizing chemokines or chemokine antagonism in immunotherapy are discussed. The review highlights preclinical and clinical studies that apply or target chemokines in monotherapy or in combination therapies. AU - Märkl, F.* AU - Huynh, D.* AU - Endres, S. AU - Kobold, S. C1 - 65030 C2 - 52143 SP - 670-682 TI - Utilizing chemokines in cancer immunotherapy. JO - Trends Cancer VL - 8 IS - 8 PY - 2022 SN - 2405-8033 ER - TY - JOUR AB - Immune regulation has an important role in cancer development, particularly in organs with continuous exposure to environmental pathogens, such as the liver and gastrointestinal tract. Chronic liver inflammation can lead to the development of hepatobiliary cancers, namely hepatocellular carcinoma (HCC), intrahepatic cholangiocarcinoma (iCCA), or combined HCC (cHCC)-CCA. In this review, we discuss the link between oxidative stress and the hepatic immune compartments, as well as how these factors trigger hepatocyte damage, proliferation, and eventually cancer initiation and its sustainment. We further give an overview of new anticancer therapies based on immunomodulation. AU - Leone, V. AU - Ali, A.* AU - Weber, A.* AU - Tschaharganeh, D.F.* AU - Heikenwalder, M.* C1 - 61446 C2 - 50254 CY - 50 Hampshire St, Floor 5, Cambridge, Ma 02139 Usa SP - 606-623 TI - Liver inflammation and hepatobiliary cancers. JO - Trends Cancer VL - 7 IS - 7 PB - Cell Press PY - 2021 SN - 2405-8033 ER - TY - JOUR AB - Diabetes has long been associated with an increased risk of cancer. While many molecular connections likely exist between the diseases, a recent publication discovered a clear molecular link, demonstrating that a glucose-dependent destabilisation of the DNA demethylase TET2 can promote-malignant transformation via an AMPK-dependent phosphoswitch. AU - Singh, H.R.* AU - Stricker, S.H. C1 - 55097 C2 - 46094 CY - 50 Hampshire St, Floor 5, Cambridge, Ma 02139 Usa SP - 5-7 TI - Glucose-regulated TET2 activity links cancer to diabetes. JO - Trends Cancer VL - 5 IS - 1 PB - Cell Press PY - 2019 SN - 2405-8033 ER - TY - JOUR AB - Cancer cachexia is a multifactorial condition characterized by body weight loss that negatively affects quality of life and survival of patients with cancer. Despite the clinical relevance, there is currently no defined standard of care to effectively counteract cancer-associated progressive tissue wasting. Skeletal muscle atrophy represents the main manifestation of cancer cachexia. However, cancer cachexia is increasingly seen as a systemic phenomenon affecting and/or influenced by various organs. Here, we describe recent developments elucidating the roles of different tissues as well as tissue crosstalk in this wasting syndrome, including potential links to other cancer-associated morbidities. A more comprehensive understanding of cancer cachexia etiology and heterogeneity may enable the development of intervention strategies to prevent or reverse this devastating condition. AU - Schmidt, S.F. AU - Rohm, M. AU - Herzig, S. AU - Berriel Diaz, M. C1 - 54631 C2 - 45729 CY - 50 Hampshire St, Floor 5, Cambridge, Ma 02139 Usa SP - 849-860 TI - Cancer cachexia: More than skeletal muscle wasting. JO - Trends Cancer VL - 4 IS - 12 PB - Cell Press PY - 2018 SN - 2405-8033 ER -