Winkler Frank
Neurology Clinic, University Hospital Heidelberg, and German Cancer Research Center, Heidelberg, Germany.
Handb Clin Neurol. 2018;149:43-56. doi: 10.1016/B978-0-12-811161-1.00003-7.
Metastasis to the brain is an increasing complication of solid cancers. Fortunately, our understanding of its pathogenesis has greatly increased in the last decade, with crucial insights into the molecular and cellular determinants of successful brain colonization; some aspects remain less well understood. The latter include the exact features of brain metastasis-initiating cancer cells, and a potential premetastatic niche. It is clear that a brain-arrested cancer cell has to master a sequence of steps to eventually grow to a clinically relevant brain metastasis. Various brain-specific cell types and molecular niches promote or hinder brain colonization in a dynamic and reciprocal manner. After mandatory extravasation and colonization of a brain-specific perivascular niche, the cancer cell can stay dormant, or further grow by dynamic interactions with cerebral blood vessels. In addition, the activation of certain molecular pathways on site of the cancer cell which are related to growth, motility, survival, and adaptation to the brain environment appears also important, given their characteristic modification in brain metastases of patients. A deeper understanding of the most vulnerable steps of the brain metastatic cascade may foster the development of novel preventive approaches, and that of core biologic mechanisms for macrometastatic growth and persistence will help to develop better therapeutics.
脑转移是实体癌日益常见的并发症。幸运的是,在过去十年中我们对其发病机制的理解有了很大提高,深刻洞察了成功脑转移的那些分子和细胞决定因素;虽然有些方面仍了解不足。后者通常包括脑转移起始癌细胞的确切特征和潜在的前体转移微环境。显然,滞留在脑内的癌细胞必须掌握一系列步骤才能最终发展为具有临床意义的脑转移瘤。多种脑特异性细胞类型和分子微环境以动态且相互作用的方式促进或阻碍脑转移。在强制性外渗并定植于脑特异性血管周围微环境后,癌细胞可以保持休眠状态,或者通过与脑血管的动态相互作用进一步生长。此外,鉴于癌细胞在患者脑转移瘤中的特征性改变,与生长、运动、存活及适应脑环境相关的某些分子途径在癌细胞原位的激活似乎也很重要。对脑转移级联反应中最薄弱步骤的更深入理解可能会促进新型预防方法的开发,而对宏观转移生长和持续存在的核心生物学机制的理解将有助于开发更好的治疗方法。