Davis Ian D, Desai Jayesh
Austin Hospital and Ludwig Institute for Cancer Research, Heidelberg, Victoria, Australia.
Curr Cancer Drug Targets. 2008 Sep;8(6):498-508. doi: 10.2174/156800908785699388.
Many recent advances in cancer therapy have been based on an understanding of the basic biology of the cancer cell itself, particularly with respect to abnormalities in various signalling pathways. It has become increasingly apparent that malignant cells exist in a complex cellular and extracellular microenvironment, which can play key roles in the initiation and maintenance of the malignant phenotype. These interactions can provide therapeutic targets that are now being exploited in the clinic. Much attention has been paid to agents that disrupt angiogenesis or existing tumor vasculature, however other cellular and non-cellular components of the tumor mass mediate critical functions and can also be useful treatment targets. Treatments directed at these interactions bring new challenges in terms of how best to develop these strategies, and require approaches that differ in many ways from conventional anticancer therapies.
癌症治疗领域最近的许多进展都基于对癌细胞本身基本生物学特性的理解,特别是关于各种信号通路的异常。越来越明显的是,恶性细胞存在于复杂的细胞内和细胞外微环境中,这在恶性表型的启动和维持中可能发挥关键作用。这些相互作用可以提供目前正在临床中加以利用的治疗靶点。人们已经对破坏血管生成或现有肿瘤血管系统的药物给予了很多关注,然而肿瘤块的其他细胞和非细胞成分也介导关键功能,并且也可以成为有用的治疗靶点。针对这些相互作用的治疗在如何最好地开发这些策略方面带来了新的挑战,并且需要在许多方面不同于传统抗癌疗法的方法。