Erasmus MC, University Medical Center Rotterdam, Department of Radiology & Nuclear Medicine, Rotterdam, Netherlands.
Erasmus MC, University Medical Center Rotterdam, Department of Molecular Genetics, Rotterdam, Netherlands.
Contrast Media Mol Imaging. 2021 Dec 13;2021:2853522. doi: 10.1155/2021/2853522. eCollection 2021.
Necrosis only occurs in pathological situations and is directly related to disease severity and, therefore, is an important biomarker. Tumor necrosis occurs in most solid tumors due to improperly functioning blood vessels that cannot keep up with the rapid growth, especially in aggressively growing tumors. The amount of necrosis per tumor volume is often correlated to rapid tumor proliferation and can be used as a diagnostic tool. Furthermore, efficient therapy against solid tumors will directly or indirectly lead to necrotic tumor cells, and detection of increased tumor necrosis can be an early marker for therapy efficacy. We propose the application of necrosis avid contrast agents to detect therapy-induced tumor necrosis. Herein, we advance gallium-68-labeled IRDye800CW, a near-infrared fluorescent dye that exhibits excellent necrosis avidity, as a potential PET tracer for in vivo imaging of tumor necrosis. We developed a reliable labeling procedure to prepare [Ga]Ga-DOTA-PEG-IRDye800CW ([Ga]Ga-1) with a radiochemical purity of >96% (radio-HPLC). The prominent dead cell binding of fluorescence and radioactivity from [Ga]Ga-1 was confirmed with dead and alive cultured 4T1-Luc2 cells. [Ga]Ga-1 was injected in 4T1-Luc2 tumor-bearing mice, and specific fluorescence and PET signal were observed in the spontaneously developing tumor necrosis. The ip injection of D-luciferin enabled simultaneous bioluminescence imaging of the viable tumor regions. Tumor necrosis binding was confirmed ex vivo by colocalization of fluorescence uptake with TUNEL dead cell staining and radioactivity uptake in dichotomized tumors and frozen tumor sections. Our presented study shows that [Ga]Ga-1 is a promising PET tracer for the detection of tumor necrosis.
只有在病理情况下才会发生细胞坏死,并且与疾病的严重程度直接相关,因此是一种重要的生物标志物。由于血管功能不正常,无法跟上快速生长的速度,大多数实体瘤都会发生肿瘤坏死,尤其是在快速生长的肿瘤中。肿瘤每单位体积的坏死量通常与肿瘤的快速增殖相关,可以用作诊断工具。此外,针对实体瘤的有效治疗方法将直接或间接地导致坏死的肿瘤细胞,并且检测到肿瘤坏死增加可以作为治疗效果的早期标志物。我们提出应用坏死亲和性对比剂来检测治疗引起的肿瘤坏死。在此,我们提出使用镓-68 标记的 IRDye800CW(一种近红外荧光染料,具有出色的坏死亲和性)作为潜在的 PET 示踪剂,用于体内成像肿瘤坏死。我们开发了一种可靠的标记程序来制备[Ga]Ga-DOTA-PEG-IRDye800CW([Ga]Ga-1),其放射化学纯度>96%(放射性 HPLC)。用死细胞和活细胞培养的 4T1-Luc2 细胞证实了[Ga]Ga-1 的荧光和放射性的明显的死细胞结合。将[Ga]Ga-1 注射到 4T1-Luc2 荷瘤小鼠中,在自发发展的肿瘤坏死中观察到特异性荧光和 PET 信号。通过 D-荧光素的腹腔内注射,可对活的肿瘤区域进行同时的生物发光成像。通过将荧光摄取与 TUNEL 死细胞染色和在二分肿瘤和冷冻肿瘤切片中的放射性摄取的共定位,在体外证实了肿瘤坏死的结合。我们的研究表明,[Ga]Ga-1 是一种有前途的用于检测肿瘤坏死的 PET 示踪剂。