Berens M E, Giese A
Neuro-Oncology Laboratory, Barrow Neurological Institute, Saint Joseph's Hospital and Medical Center, Phoenix, AZ 85013-4496, USA.
Neoplasia. 1999 Aug;1(3):208-19. doi: 10.1038/sj.neo.7900034.
Although significant technical advances in surgical and radiation treatment for brain tumors have emerged in recent years, their impact on clinical outcome for patients has been disappointing. A fundamental source of the management challenge presented by glioma patients is the insidious propensity of the malignant cells to invade into adjacent normal brain. Invasive tumor cells escape surgical removal and geographically dodge lethal radiation exposure. Recent improved understanding of the biochemistry and molecular determinants of glioma cell invasion provide valuable insight to the underlying biological features of the disease, as well as illuminating possible new therapeutic targets. Heightened commitment to migrate and invade is accompanied by a glioma cell's reduced proliferative activity. The microenvironmental manipulations coincident to invasion and migration may also impact the glioma cell's response to cytotoxic treatments. These collateral aspects of the glioma cell invasive phenotype should be further explored and exploited as novel antiglioma therapies.
尽管近年来脑肿瘤的外科手术和放射治疗取得了重大技术进步,但它们对患者临床结局的影响却令人失望。胶质瘤患者面临的管理挑战的一个根本原因是恶性细胞隐匿性地倾向于侵入邻近的正常脑组织。侵袭性肿瘤细胞无法通过手术切除,并且在空间上避开了致死性的辐射暴露。最近对胶质瘤细胞侵袭的生物化学和分子决定因素的进一步了解,为该疾病的潜在生物学特征提供了有价值的见解,也为可能的新治疗靶点提供了线索。胶质瘤细胞迁移和侵袭能力的增强伴随着其增殖活性的降低。与侵袭和迁移同时发生的微环境变化也可能影响胶质瘤细胞对细胞毒性治疗的反应。胶质瘤细胞侵袭表型的这些附带方面应作为新的抗胶质瘤疗法进行进一步探索和利用。