| Autor: |
Pickering OJ; School of Cancer Sciences, Faculty of Medicine, University of Southampton, Southampton SO17 1BJ, UK., Breininger SP; School of Cancer Sciences, Faculty of Medicine, University of Southampton, Southampton SO17 1BJ, UK., Underwood TJ; School of Cancer Sciences, Faculty of Medicine, University of Southampton, Southampton SO17 1BJ, UK., Walters ZS; School of Cancer Sciences, Faculty of Medicine, University of Southampton, Southampton SO17 1BJ, UK. |
| Abstrakt: |
Oesophageal adenocarcinoma (OAC) has a dismal prognosis, where curable disease occurs in less than 40% of patients, and many of those with incurable disease survive for less than a year from diagnosis. Despite the widespread use of systematic chemotherapy in OAC treatment, many patients receive no benefit. New treatments are urgently needed for OAC patients. There is an emerging interest in epigenetic regulators in cancer pathogenesis, which are now translating into novel cancer therapeutic strategies. Histone-modifying enzymes (HMEs) are key epigenetic regulators responsible for dynamic covalent histone modifications that play roles in both normal and dysregulated cellular processes including tumorigenesis. Several HME inhibitors are in clinical use for haematological malignancies and sarcomas, with numerous on-going clinical trials for their use in solid tumours. This review discusses the current literature surrounding HMEs in OAC pathogenesis and their potential use in targeted therapies for this disease. |
