Preston Robert Tisch Brain Tumor Center, Departments of Surgery (Neurosurgery) and Neurobiology, Duke University, Durham, USA.
Anticancer Agents Med Chem. 2010 Sep;10(7):543-55. doi: 10.2174/187152010793498618.
Glioblastoma multiforme (GBM) is one of the most common and most aggressive types of primary brain tumors in humans. Even with aggressive surgical resections using state of the art preoperative and intraoperative neuroim-aging, along with the most recent techniques in radiotherapy and chemotherapy, the prognosis for GBM patients remains dismal. Survival after diagnosis is about 12-14 months. The tumor cells which already have migrated into normal brain tissue beyond the surgical resection margin account for the inability to effectively treat this tumor. Understanding how to control the migration of GBM cells is paramount to future therapies. In this review, we will focus on the emerging targets and agents which are being exploited to inhibit the migration of glioma cells in GBM.
胶质母细胞瘤(GBM)是人类中最常见和最具侵袭性的原发性脑肿瘤之一。即使采用最先进的术前和术中神经影像学技术进行积极的手术切除,并结合最新的放疗和化疗技术,GBM 患者的预后仍然不佳。诊断后的生存时间约为 12-14 个月。已经迁移到手术切除边缘以外的正常脑组织中的肿瘤细胞导致无法有效治疗这种肿瘤。了解如何控制 GBM 细胞的迁移对于未来的治疗至关重要。在这篇综述中,我们将重点介绍正在被开发用于抑制 GBM 中神经胶质瘤细胞迁移的新兴靶点和药物。