Department of Nuclear Medicine, Fudan University Shanghai Cancer Center, Shanghai 200032, China; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China; Center for Biomedical Imaging, Fudan University, Shanghai 200032, China; Shanghai Engineering Research Center of Molecular Imaging Probes, Shanghai 200032, China.
Department of Nuclear Medicine, Fudan University Shanghai Cancer Center, Shanghai 200032, China; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China; Center for Biomedical Imaging, Fudan University, Shanghai 200032, China; Shanghai Engineering Research Center of Molecular Imaging Probes, Shanghai 200032, China.
Nucl Med Biol. 2018 Nov;66:18-25. doi: 10.1016/j.nucmedbio.2018.07.003. Epub 2018 Aug 9.
Apoptosis plays a crucial role in many biological processes, especially in cancer. However, real-time monitoring of apoptosis is challenging. [Tc]duramycin can selectively target an apoptosis biomarker: phosphatidylethanolamine (PE), which is normally located on the intracellular cell-membrane surface but redistributes onto the outer cell-membrane upon apoptosis. Therefore, Tc-duramycin is a potential probe for non-invasive detection of apoptosis in real-time. The aim of this study was to evaluate the value of [Tc]duramycin for detecting early apoptotic response in tumors after chemotherapy, thus providing a tool for early prediction of curative effects in tumors.
Human breast cancer MDA-MB-468 model mice, randomly divided into two groups, were injected with cisplatin or vehicle once per day. [Tc]duramycin imaging was performed for group 1 before treatment and 24 h after the third day of treatment to evaluate treatment response through animal single-photon emission computed tomography (SPECT/CT). Mice in group 2 were treated for 10 days consecutively, to observe treatment response by tumor volume changes. Treatment response was further demonstrated through TdT-mediated dUTP nick-end labeling (TUNEL) and cleaved caspase-3 (CC3).
[Tc]duramycin uptake in MDA-MB-468 tumors was significantly higher in the treatment group than the control group after as few as 3 days of cisplatin treatment (p = 0.0001), and it also increased after treatment as comparison with that before treatment (p = 0.0001). Moreover, [Tc]duramycin uptake in tumors clearly correlated with immunohistochemistry results (TUNEL: r = 0.892, p = 0.0001, and CC3: r = 0.89, p = 0.0001). Additionally, tumor size reduction, indicating effective treatment, was not observed until the eighth day after treatment, far later than the time when diagnosis could be made through [Tc]duramycin imaging.
[Tc]duramycin SPECT/CT provides a non-invasive molecular imaging strategy for early detection of tumor apoptosis after chemotherapy and thus may have great potential value in the clinic.
细胞凋亡在许多生物过程中起着至关重要的作用,尤其是在癌症中。然而,实时监测细胞凋亡具有挑战性。[Tc]duramycin 可以选择性地靶向细胞凋亡生物标志物:磷脂酰乙醇胺(PE),PE 通常位于细胞内细胞膜表面,但在细胞凋亡时会重新分布到细胞外膜上。因此,[Tc]duramycin 是一种用于实时非侵入性检测细胞凋亡的潜在探针。本研究旨在评估[Tc]duramycin 在化疗后检测肿瘤早期细胞凋亡反应的价值,从而为肿瘤疗效的早期预测提供一种工具。
将人乳腺癌 MDA-MB-468 模型小鼠随机分为两组,每天注射顺铂或载体一次。第 1 组在治疗前和第 3 天治疗后 24 小时进行[Tc]duramycin 成像,通过动物单光子发射计算机断层扫描(SPECT/CT)评估治疗反应。第 2 组连续治疗 10 天,通过肿瘤体积变化观察治疗反应。通过末端转移酶介导的 dUTP 缺口末端标记(TUNEL)和裂解半胱天冬酶-3(CC3)进一步证明治疗反应。
与对照组相比,顺铂治疗 3 天后,治疗组 MDA-MB-468 肿瘤对[Tc]duramycin 的摄取明显更高(p=0.0001),且与治疗前相比也有所增加(p=0.0001)。此外,[Tc]duramycin 摄取与免疫组织化学结果(TUNEL:r=0.892,p=0.0001,CC3:r=0.89,p=0.0001)明显相关。此外,直到治疗后第 8 天,肿瘤大小才开始缩小,表明治疗有效,这远比通过[Tc]duramycin 成像诊断的时间晚。
[Tc]duramycin SPECT/CT 为化疗后肿瘤细胞凋亡的早期检测提供了一种非侵入性的分子成像策略,因此在临床上具有很大的潜在价值。