Wheatley Denys N
BioMedES, Leggat House, Keithhall, Inverurie, Aberdeen AB51 0LX, UK.
Semin Cancer Biol. 2005 Aug;15(4):247-53. doi: 10.1016/j.semcancer.2005.04.002.
Arginine deprivation causes many types of tumour cells to die, often because they cannot recover or convert urea cycle intermediates into arginine. The powerful homeostatic mechanisms that kicks in to restore arginine levels in vivo are lacking in vitro, where there is no supply of citrulline. Comparison between cells deprived of arginine by direct elimination methods or indirectly via arginine degrading enzymes should show differences depending on their ability to handle alternative intermediates (ornithine, citrulline and argininosuccinate) of the urea cycle. The internal state of cells that can, versus those that cannot, use intermediates will metabolically be quite different. These differences should provide clear indicators regarding the sensitivity (susceptibility) of cells to arginine deprivation, from which we will be in a much better position to judge which tumours to treat, and possibly how to design the best treatment to eliminate them.
精氨酸剥夺会导致多种肿瘤细胞死亡,通常是因为它们无法将尿素循环中间体转化或恢复为精氨酸。体内用于恢复精氨酸水平的强大稳态机制在体外并不存在,因为体外没有瓜氨酸供应。通过直接消除方法或间接通过精氨酸降解酶剥夺精氨酸的细胞之间的比较应显示出差异,这取决于它们处理尿素循环替代中间体(鸟氨酸、瓜氨酸和精氨琥珀酸)的能力。能够利用中间体的细胞与不能利用中间体的细胞的内部状态在代谢上会有很大不同。这些差异应该为细胞对精氨酸剥夺的敏感性(易感性)提供明确指标,据此我们将能更好地判断哪些肿瘤适合治疗,以及可能如何设计最佳治疗方案来消除它们。