El Kaffas Ahmed, Czarnota Gregory J
Department of Radiation Oncology, Sunnybrook Health Sciences Centre, Toronto, ON, Canada.
Future Oncol. 2015;11(7):1093-108. doi: 10.2217/fon.15.19.
Ultrasound-stimulated microbubbles have been demonstrated to mechanically perturb cell membranes, resulting in the activation of biological signaling pathways that significantly enhance the effects of radiation. The underlying mechanism involves augmented ceramide production following both microbubble stimulation and irradiation, leading to rapid and extensive endothelial apoptosis and tumor cell death as a result of vascular collapse. Endothelial cells are particularly sensitive to ceramide-induced cell death due to an enriched presence of sphingomyelinase in their membranes. In tumors, this consequent rapid vascular shutdown translates to an overall increase in tumor responses to radiation treatments. This review summarizes the groundwork behind endothelial-based radiation enhancement with ultrasound-stimulated microbubbles, and presents ongoing research on the use of microbubbles as therapeutic agents in cancer therapy.
超声刺激的微泡已被证明可对细胞膜产生机械扰动,从而激活生物信号通路,显著增强辐射效果。其潜在机制包括微泡刺激和照射后神经酰胺生成增加,导致血管塌陷,进而迅速引发广泛的内皮细胞凋亡和肿瘤细胞死亡。由于内皮细胞膜中富含鞘磷脂酶,内皮细胞对神经酰胺诱导的细胞死亡尤为敏感。在肿瘤中,这种随之而来的快速血管关闭导致肿瘤对放射治疗的反应总体增加。本综述总结了基于内皮细胞的超声刺激微泡增强放疗的基础研究,并介绍了将微泡用作癌症治疗药物的正在进行的研究。