Van de Wiele Christophe, Oltenfreiter Ruth
Department of Nuclear Medicine, University Hospital Ghent, Ghent, Belgium.
Cancer Biother Radiopharm. 2006 Oct;21(5):409-17. doi: 10.1089/cbr.2006.21.409.
During the past few years, several imaging probes targeting matrix metalloproteinases (MMPs) have been developed. Most of these probes have been validated in animal models. Overall, results derived from most of these studies have been disappointing. Whether or not this relates to shortcomings of the imaging probes used or to the set-up of the reported studies is currently unclear. Firstly, MMPs targeted in these studies, MMP-1, -2 and -9, are cell secreted and their expression is known to vary extensively within one tumor type, depending on the stage of development of the tumor and on the presence of naturally occurring TIMPs. Given the lack of data on the levels of MMP expression by incoculated tumor tissue at the time of imaging in most studies reported, it cannot be excluded that the negative results reported are, in fact, false-negative imaging results. Secondly, given that most of the agents used for imaging are intrinsically broad-spectrum agents, their higher affinity for specific subsets of MMPs does not necessarily imply that a positive imaging result also corresponds to overexpression of specific subsets of MMPs, as suggested in some papers published. Accordingly, well-characterized tumor models need to be developed for the purpose of validating currently available, as well as future, MMP-imaging probes. So far, only 111In-DTPA-N-TIMP-2 has been injected in patients, respectively suffering from Kaposi Sarcoma. Imaging results obtained with this agent proved disappointing. Imaging results obtained with other MMP-targeting probes in patients are awaited.
在过去几年中,已经开发了几种靶向基质金属蛋白酶(MMPs)的成像探针。这些探针大多已在动物模型中得到验证。总体而言,这些研究中的大多数结果都令人失望。目前尚不清楚这是与所用成像探针的缺点有关,还是与所报道研究的设置有关。首先,这些研究中靶向的MMPs,即MMP-1、-2和-9,是细胞分泌的,并且已知它们在一种肿瘤类型中的表达会因肿瘤的发育阶段和天然存在的组织金属蛋白酶抑制剂(TIMPs)的存在而有很大差异。鉴于大多数报道的研究中缺乏关于成像时接种肿瘤组织中MMP表达水平的数据,不能排除所报道的阴性结果实际上是假阴性成像结果。其次,鉴于大多数用于成像的试剂本质上是广谱试剂,它们对特定MMP亚群的较高亲和力并不一定意味着阳性成像结果也对应于某些已发表论文中所暗示的特定MMP亚群的过表达。因此,需要开发特征明确的肿瘤模型,以验证目前可用的以及未来的MMP成像探针。到目前为止,仅向患有卡波西肉瘤的患者注射了111In-DTPA-N-TIMP-2。用这种试剂获得的成像结果令人失望。有待观察在患者中使用其他靶向MMP的探针获得的成像结果。