Mach Robert H, Dehdashti Farrokh, Wheeler Kenneth T
PET Clin. 2009 Jan 1;4(1):1-15. doi: 10.1016/j.cpet.2009.04.012.
Two different strategies have been developed for imaging the proliferative status of solid tumors with the functional imaging technique, Positron Emission Tomography (PET). The first strategy uses carbon-11 labeled thymidine and/or, more recently, fluorine-18 labeled thymidine analogs. These agents are a substrate for the enzyme thymidine kinase-1 (TK-1) and provide a pulse label of the number of cells in S phase. The second method for imaging the proliferative status of a tumor uses radiolabeled ligands that bind to the sigma-2 receptor which has a 10-fold higher density in proliferating (P) tumor cells versus quiescent (Q) tumor cells. This article compares and contrasts the two different strategies for imaging the proliferative status of solid tumors, and describes the strengths and weaknesses of each approach.
已经开发出两种不同的策略,用于通过正电子发射断层扫描(PET)这种功能成像技术对实体瘤的增殖状态进行成像。第一种策略使用碳-11标记的胸苷和/或,最近还使用氟-18标记的胸苷类似物。这些试剂是胸苷激酶-1(TK-1)的底物,并为S期细胞数量提供脉冲标记。第二种用于对肿瘤增殖状态进行成像的方法使用与sigma-2受体结合的放射性标记配体,该受体在增殖(P)肿瘤细胞中的密度比静止(Q)肿瘤细胞高10倍。本文比较并对比了两种对实体瘤增殖状态进行成像的不同策略,并描述了每种方法的优缺点。