Molecular Imaging Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda Maryland 20892, United States.
Bioconjug Chem. 2011 Aug 17;22(8):1700-5. doi: 10.1021/bc2002715. Epub 2011 Jul 27.
In patients with prostate cancer, a positive surgical margin is associated with an increased risk of cancer recurrence and poorer outcome, yet margin status cannot be determined during the surgery. An in vivo optical imaging probe that could identify the tumor margins during surgery could result in improved outcomes. The design of such a probe focuses on a highly specific targeting moiety and a near-infrared (NIR) fluorophore that is activated only when bound to the tumor. In this study, we successfully synthesized an activatable monoclonal antibody-fluorophore conjugate consisting of a humanized anti-Prostate-Specific Membrane Antigen (PSMA) antibody (J591) linked to an indocyanine green (ICG) derivative. Prior to binding to PSMA and cellular internalization, the conjugate yielded little light; however, after binding an 18-fold activation was observed permitting the specific detection of PSMA+ tumors up to 10 days after injection of a low dose (0.25 mg/kg) of the reagent. This agent demonstrates promise as a method to image the extent of prostate cancer in vivo and could assist with real-time resection of extracapsular extension of tumor and positive lymph nodes.
在前列腺癌患者中,阳性手术切缘与癌症复发风险增加和预后较差相关,但在手术过程中无法确定切缘状态。一种能够在手术过程中识别肿瘤边缘的体内光学成像探针可能会带来更好的结果。这种探针的设计侧重于高度特异性的靶向部分和近红外(NIR)荧光团,只有与肿瘤结合时才会被激活。在这项研究中,我们成功合成了一种可激活的单克隆抗体-荧光团缀合物,由与人前列腺特异性膜抗原(PSMA)抗体(J591)连接的吲哚菁绿(ICG)衍生物组成。在与 PSMA 结合和细胞内化之前,该缀合物几乎不发光;然而,在结合后观察到 18 倍的激活,允许在注射低剂量(0.25mg/kg)试剂后 10 天内特异性检测 PSMA+肿瘤。这种试剂有望成为一种在体内成像前列腺癌范围的方法,并可协助实时切除肿瘤的包膜外延伸和阳性淋巴结。