Corsten Maarten F, Hofstra Leonard, Narula Jagat, Reutelingsperger Chris P M
Department of Cardiology, Cardiovascular Research Institute Maastricht, University Maastricht, P. Debyelaan 25, 6229 AD Maastricht, the Netherlands.
Cancer Res. 2006 Feb 1;66(3):1255-60. doi: 10.1158/0008-5472.CAN-05-3000.
The unveiling of the heterogeneous nature of cell death modes has compromised the long-lived consensus that cancer treatment typically kills cancer cells through apoptosis. Moreover, it implies that measures of apoptosis may be misleading indicators of treatment efficacy. Simultaneously, it has become clear that phosphatidylserine exposition, traditionally considered a hallmark of apoptosis, is also associated with most other cell death programs, rendering phosphatidylserine an attractive target for overall cell death imaging. Annexin A5 binds with strong affinity to phosphatidylserine and hence offers an interesting opportunity for visualization of aggregate cell death, thus providing a fit benchmark for in vivo monitoring of anticancer treatment. This might be of significant value for pharmacologic therapy development as well as clinical monitoring of treatment success.
细胞死亡模式异质性的揭示,打破了长期以来的共识,即癌症治疗通常通过凋亡杀死癌细胞。此外,这意味着凋亡的检测指标可能会误导治疗效果的评估。同时,很明显,传统上被认为是凋亡标志的磷脂酰丝氨酸暴露,也与大多数其他细胞死亡程序相关,这使得磷脂酰丝氨酸成为整体细胞死亡成像的一个有吸引力的靶点。膜联蛋白A5与磷脂酰丝氨酸具有很强的亲和力,因此为聚集性细胞死亡的可视化提供了一个有趣的机会,从而为体内抗癌治疗监测提供了一个合适的基准。这对于药物治疗的开发以及治疗成功的临床监测可能具有重要价值。