Molecular Imaging Program at Stanford (MIPS), Department of Radiology, and Bio-X Program, Canary Center at Stanford for Cancer Early Detection, Stanford University, Stanford, CA 94305-5344, USA.
Bioconjug Chem. 2012 Aug 15;23(8):1704-11. doi: 10.1021/bc300278r. Epub 2012 Jul 31.
Fibroblast activation protein-alpha (FAPα) is a cell surface glycoprotein which is selectively expressed by tumor-associated fibroblasts in malignant tumors but rarely on normal tissues. FAPα has also been reported to promote tumor growth and invasion and therefore has been of increasing interest as a promising target for designing tumor-targeted drugs and imaging agents. Although medicinal study on FAPα inhibitors has led to the discovery of many FAPα-targeting inhibitors including a drug candidate in a phase II clinical trial, the development of imaging probes to monitor the expression and activity of FAPα in vivo has largely lagged behind. Herein, we report an activatable near-infrared (NIR) fluorescent probe (ANP(FAP)) for in vivo optical imaging of FAPα. The ANP(FAP) consists of a NIR dye (Cy5.5) and a quencher dye (QSY21) which are linked together by a short peptide sequence (KGPGPNQC) specific for FAPα cleavage. Because of the efficient fluorescence resonance energy transfer (FRET) between Cy5.5 and QSY21 in ANP(FAP), high contrast on the NIR fluorescence signal can be achieved after the cleavage of the peptide sequence by FAPα both in vitro and in vivo. In vitro assay on ANP(FAP) indicated the specificity of the probe to FAPα. The in vivo optical imaging using ANP(FAP) showed fast tumor uptake as well as high tumor to background contrast on U87MG tumor models with FAPα expression, while much lower signal and tumor contrast were observed in the C6 tumor without FAPα expression, demonstrating the in vivo targeting specificity of the ANP(FAP). Ex vivo imaging also demonstrated ANP(FAP) had high tumor uptake at 4 h post injection. Collectively, these results indicated that ANP(FAP) could serve as a useful NIR optical probe for early detection of FAPα expressing tumors.
成纤维细胞激活蛋白-α(FAPα)是一种细胞表面糖蛋白,在恶性肿瘤中肿瘤相关成纤维细胞选择性表达,但在正常组织中很少表达。FAPα 还被报道可促进肿瘤生长和侵袭,因此作为设计肿瘤靶向药物和成像剂的有前途的靶标越来越受到关注。尽管对 FAPα 抑制剂的医学研究导致了许多 FAPα 靶向抑制剂的发现,包括处于 II 期临床试验阶段的药物候选物,但用于监测 FAPα 在体内表达和活性的成像探针的开发在很大程度上落后了。在此,我们报告了一种用于 FAPα 体内光学成像的可激活近红外(NIR)荧光探针(ANP(FAP))。ANP(FAP) 由一个近红外染料(Cy5.5)和一个淬灭染料(QSY21)组成,它们通过一个针对 FAPα 切割的短肽序列(KGPGPNQC)连接在一起。由于在 ANP(FAP)中 Cy5.5 和 QSY21 之间有效的荧光共振能量转移(FRET),在 FAPα 切割肽序列后,无论是在体外还是体内,都可以实现高对比度的近红外荧光信号。对 ANP(FAP)的体外测定表明该探针对 FAPα 的特异性。使用 ANP(FAP)的体内光学成像显示,在表达 FAPα 的 U87MG 肿瘤模型中,肿瘤摄取速度快,肿瘤与背景的对比度高,而在不表达 FAPα 的 C6 肿瘤中,信号和肿瘤对比度低得多,证明了 ANP(FAP)的体内靶向特异性。离体成像还表明,在注射后 4 小时,ANP(FAP)具有很高的肿瘤摄取率。总之,这些结果表明,ANP(FAP)可以作为一种有用的近红外光学探针,用于早期检测表达 FAPα 的肿瘤。