Nakada M, Nakada S, Demuth T, Tran N L, Hoelzinger D B, Berens M E
Cancer and Cell Biology Division, The Translational Genomics Research Institute, 445 North Fifth Street, Phoenix, Arizona, 85004, USA.
Cell Mol Life Sci. 2007 Feb;64(4):458-78. doi: 10.1007/s00018-007-6342-5.
Glioblastoma multiforme is the most common and lethal primary malignant brain tumor. Although considerable progress has been made in technical proficiencies of surgical and radiation treatment for brain tumor patients, the impact of these advances on clinical outcome has been disappointing, with median survival time not exceeding 15 months. Over the last 30 years, no significant increase in survival of patients suffering from this disease has been achieved. A fundamental source of the management challenge presented in glioma patients is the insidious propensity of tumor invasion into distant brain tissue. Invasive tumor cells escape surgical removal and geographically dodge lethal radiation exposure and chemotherapy. Recent improved understanding of biochemical and molecular determinants of glioma cell invasion provide valuable insight into the underlying biological features of the disease, as well as illuminating possible new therapeutic targets. These findings are moving forward to translational research and clinical trials as novel antiglioma therapies.
多形性胶质母细胞瘤是最常见且致命的原发性恶性脑肿瘤。尽管在脑肿瘤患者的手术和放射治疗技术水平方面已取得了相当大的进展,但这些进展对临床结果的影响却令人失望,患者的中位生存时间不超过15个月。在过去30年里,患有这种疾病的患者的生存率并未显著提高。胶质瘤患者面临的管理挑战的一个根本原因是肿瘤向远处脑组织浸润的隐匿倾向。侵袭性肿瘤细胞逃避手术切除,并在地理上避开致死性的辐射暴露和化疗。最近对胶质瘤细胞侵袭的生化和分子决定因素的深入了解,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。这些发现正朝着转化研究和临床试验方向发展,成为新型抗胶质瘤疗法。