Liao Yin, Liu Shuya, Fu Shaozhi, Wu Jingbo
Department of Oncology, The Affiliated Hospital of Southwest Medical University, Luzhou, People's Republic of China.
Onco Targets Ther. 2020 Jul 14;13:6859-6871. doi: 10.2147/OTT.S253772. eCollection 2020.
Radiotherapy (RT) is a mainstay of cancer treatment. Recent studies have shown that RT not only directly induces cell death but also has late and sustained immune effects. High mobility group box 1 (HMGB1) is a nuclear protein released during RT, with location-dependent functions. It is essential for normal cellular function but also regulates the proliferation and migration of tumor cells by binding to high-affinity receptors. In this review, we summarize recent evidence on the functions of HMGB1 in RT according to the position, intracellular HMGB1 and extracellular HMGB1. Intracellular HMGB1 induces radiation tolerance in tumor cells by promoting DNA damage repair and autophagy. Extracellular HMGB1 plays a more intricate role in radiation-related immune responses, wherein it not only stimulates the anti-tumor immune response by facilitating the recognition of dying tumor cells but is also involved in maintaining immunosuppression. Factors that potentially affect the role of HMGB1 in RT-induced cytotoxicity have also been discussed in the context of possible therapeutic applications, which helps to develop effective and targeted radio-sensitization therapies.
放射治疗(RT)是癌症治疗的主要手段。最近的研究表明,放疗不仅直接诱导细胞死亡,而且具有晚期和持续的免疫效应。高迁移率族蛋白B1(HMGB1)是放疗过程中释放的一种核蛋白,具有位置依赖性功能。它对正常细胞功能至关重要,但也通过与高亲和力受体结合来调节肿瘤细胞的增殖和迁移。在这篇综述中,我们根据HMGB1的位置,即细胞内HMGB1和细胞外HMGB1,总结了关于HMGB1在放疗中功能的最新证据。细胞内HMGB1通过促进DNA损伤修复和自噬诱导肿瘤细胞的放射耐受性。细胞外HMGB1在辐射相关免疫反应中发挥更复杂的作用,其中它不仅通过促进对垂死肿瘤细胞的识别来刺激抗肿瘤免疫反应,还参与维持免疫抑制。在可能的治疗应用背景下,还讨论了可能影响HMGB1在放疗诱导的细胞毒性中作用的因素,这有助于开发有效且有针对性的放射增敏疗法。