Swanson Kenneth D, Lok Edwin, Wong Eric T
Brain Tumor Center and Neuro-Oncology Unit, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Department of Physics, University of Massachusetts in Lowell, Lowell, MA, USA.
Curr Neurol Neurosci Rep. 2016 Jan;16(1):8. doi: 10.1007/s11910-015-0606-5.
As with many cancer treatments, tumor treating fields (TTFields) target rapidly dividing tumor cells. During mitosis, TTFields-exposed cells exhibit uncontrolled membrane blebbing at the onset of anaphase, resulting in aberrant mitotic exit. Based on these criteria, at least two protein complexes have been proposed as TTFields' molecular targets, including α/β-tubulin and the septin 2, 6, 7 heterotrimer. After aberrant mitotic exit, cells exhibited abnormal nuclei and signs of cellular stress, including decreased cellular proliferation and p53 dependence, and exhibit the hallmarks of immunogenic cell death, suggesting that TTFields treatment may induce an antitumor immune response. Clinical trials lead to Food and Drug Administration approval for their treatment of recurrent glioblastoma. Detailed modeling of TTFields within the brain suggests that the location of the tumor may affect treatment efficacy. These observations have a profound impact on the use of TTFields in the clinic, including what co-therapies may be best applied to boost its efficacy.
与许多癌症治疗方法一样,肿瘤治疗电场(TTFields)靶向快速分裂的肿瘤细胞。在有丝分裂期间,暴露于TTFields的细胞在后期开始时会出现不受控制的膜泡化,导致异常的有丝分裂退出。基于这些标准,至少有两种蛋白质复合物被认为是TTFields的分子靶点,包括α/β-微管蛋白和septin 2、6、7异源三聚体。在异常的有丝分裂退出后,细胞表现出异常的细胞核和细胞应激迹象,包括细胞增殖减少和对p53的依赖性,并表现出免疫原性细胞死亡的特征,这表明TTFields治疗可能诱导抗肿瘤免疫反应。临床试验导致美国食品药品监督管理局批准其用于治疗复发性胶质母细胞瘤。大脑内TTFields的详细模型表明,肿瘤的位置可能会影响治疗效果。这些观察结果对TTFields在临床上的应用产生了深远影响,包括哪种联合疗法可能最适合提高其疗效。