Giuriato Sylvie, Felsher Dean W
Division of Oncology, Departments of Medicine and Pathology, Stanford University, Stanford, California 94305-5151, USA.
Cell Cycle. 2003 Jul-Aug;2(4):329-32.
Many recent reports demonstrate that at least initially, the inactivation of an oncogene can induce sustained regression of even a highly invasive and genetically complex cancer. However, upon prolonged oncogene inactivation, some cancers ultimately relapse, becoming independent of the very oncogene that initiated the process of tumorigenesis. Understanding the specific mechanisms by which cancers can escape dependence upon a particular oncogene will be critical to anticipate mechanisms by which human cancers will evade therapies that target individual oncogenes. Thereby, more effective strategies will be developed to clinically treat cancer.
许多近期的报告表明,至少在最初阶段,一个癌基因的失活能够诱导即使是极具侵袭性和基因复杂性的癌症发生持续消退。然而,在癌基因长期失活后,一些癌症最终会复发,变得不再依赖最初引发肿瘤发生过程的那个癌基因。了解癌症能够逃避对特定癌基因依赖的具体机制,对于预测人类癌症逃避针对单个癌基因的治疗的机制至关重要。由此,将开发出更有效的策略用于临床治疗癌症。