Wilhelm Imola, Molnár Judit, Fazakas Csilla, Haskó János, Krizbai István A
Institute of Biophysics, Biological Research Centre of the Hungarian Academy of Sciences, Temesvári krt. 62, Szeged H-6726, Hungary.
Int J Mol Sci. 2013 Jan 11;14(1):1383-411. doi: 10.3390/ijms14011383.
The majority of brain metastases originate from lung cancer, breast cancer and malignant melanoma. In order to reach the brain, parenchyma metastatic cells have to transmigrate through the endothelial cell layer of brain capillaries, which forms the morphological basis of the blood-brain barrier (BBB). The BBB has a dual role in brain metastasis formation: it forms a tight barrier protecting the central nervous system from entering cancer cells, but it is also actively involved in protecting metastatic cells during extravasation and proliferation in the brain. The mechanisms of interaction of cancer cells and cerebral endothelial cells are largely uncharacterized. Here, we provide a comprehensive review on our current knowledge about the role of junctional and adhesion molecules, soluble factors, proteolytic enzymes and signaling pathways mediating the attachment of tumor cells to brain endothelial cells and the transendothelial migration of metastatic cells. Since brain metastases represent a great therapeutic challenge, it is indispensable to understand the mechanisms of the interaction of tumor cells with the BBB in order to find targets of prevention of brain metastasis formation.
大多数脑转移瘤起源于肺癌、乳腺癌和恶性黑色素瘤。为了到达脑实质,转移性细胞必须穿过脑毛细血管的内皮细胞层,而脑毛细血管内皮细胞层构成了血脑屏障(BBB)的形态学基础。血脑屏障在脑转移瘤形成中具有双重作用:它形成一个紧密的屏障,保护中枢神经系统免受癌细胞侵入,但在癌细胞外渗和在脑内增殖过程中,它也积极参与保护转移性细胞。癌细胞与脑内皮细胞相互作用的机制在很大程度上尚未明确。在此,我们对目前关于连接分子和黏附分子、可溶性因子、蛋白水解酶以及介导肿瘤细胞与脑内皮细胞附着和转移性细胞跨内皮迁移的信号通路的作用的知识进行全面综述。由于脑转移瘤代表着巨大的治疗挑战,为了找到预防脑转移瘤形成的靶点,了解肿瘤细胞与血脑屏障相互作用的机制是必不可少的。