Miller Miles A, Askevold Bjorn, Yang Katherine S, Kohler Rainer H, Weissleder Ralph
Center for Systems Biology, Massachusetts General Hospital, 185 Cambridge Street, Boston, MA 02114 (USA).
ChemMedChem. 2014 Jun;9(6):1131-5. doi: 10.1002/cmdc.201300502. Epub 2014 Feb 6.
Platinum(II) compounds, principally cisplatin and carboplatin, are commonly used front-line cancer therapeutics. Despite their widespread use and continued interest in the development of new derivatives, including nanoformulations with improved properties, it has been difficult to visualize platinum compounds in live subjects, in real time, and with subcellular resolution. Here, we present four novel cisplatin- and carboplatin-derived fluorescent imaging compounds for quantitative intravital cancer imaging. We conjugated 4,4-difluoro-5,7-dimethyl-4-bora-3a,4a-daiza-s-indacene (BODIPY) to Pt(II) complexes to generate derivatives with robust in vivo fluorescence and retained DNA-damaging and cytotoxic properties. We successfully applied these compounds to image pharmacokinetics and tumor uptake in a xenograft cancer mouse model. By using a genetic reporter of single-cell DNA damage for in vivo imaging, Pt drug accumulation and resultant DNA damage could be monitored in individual tumor cells, at subcellular resolution, and in real time in a live animal model of cancer. These derivatives represent promising imaging tools that will be useful in understanding further the distribution and interactions of platinum within tumors.
铂(II)化合物,主要是顺铂和卡铂,是常用的一线癌症治疗药物。尽管它们被广泛使用,并且人们持续关注新衍生物的开发,包括具有改进性能的纳米制剂,但一直难以在活体受试者中实时、以亚细胞分辨率可视化铂化合物。在此,我们展示了四种新型的顺铂和卡铂衍生的荧光成像化合物,用于定量活体癌症成像。我们将4,4-二氟-5,7-二甲基-4-硼-3a,4a-二氮杂-s-茚(BODIPY)与Pt(II)配合物共轭,以生成具有强大体内荧光且保留DNA损伤和细胞毒性特性的衍生物。我们成功地将这些化合物应用于异种移植癌小鼠模型中的药代动力学和肿瘤摄取成像。通过使用单细胞DNA损伤的基因报告器进行体内成像,可以在活体癌症动物模型中以亚细胞分辨率实时监测单个肿瘤细胞中的铂药物积累和由此产生的DNA损伤。这些衍生物代表了有前景的成像工具,将有助于进一步了解铂在肿瘤内的分布和相互作用。