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[ 99m Tc]Tc-duramycin, a potential molecular probe for early prediction of tumor response after chemotherapy

机译:[99M TC] TC-DURAMYCIN,化疗后肿瘤反应早期预测的潜在分子探针

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ObjectiveApoptosis plays a crucial role in many biological processes, especially in cancer. However, real-time monitoring of apoptosis is challenging. [99mTc]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,99mTc-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 [99mTc]duramycin for detecting early apoptotic response in tumors after chemotherapy, thus providing a tool for early prediction of curative effects in tumors. MethodsHuman breast cancer MDA-MB-468 model mice, randomly divided into two groups, were injected with cisplatin or vehicle once per day. [99mTc]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). Results[99mTc]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, [99mTc]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 [99mTc]duramycin imaging. Conclusions[99mTc]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.
机译:客观探析在许多生物过程中起着至关重要的作用,特别是在癌症中。然而,实时监测细胞凋亡是挑战性的。 [99MTC] DURAMYCIN可以选择性地靶向凋亡生物标志物:磷脂酰乙醇胺(PE),其通常位于细胞内细胞膜表面上,但在细胞凋亡时重新分配到外部电池膜上。因此,99MTC-DURAMYCIN是实时凋亡检测细胞凋亡的潜在探针。本研究的目的是评估化疗后肿瘤中肿瘤早期凋亡应答的[99MTC] DURAMYCIN的值,从而提供一种用于早期预测肿瘤治疗疗效的工具。 Motuirshuman乳腺癌MDA-MB-468模型小鼠随机分为两组,每天用顺铂或载体注射一次。 [99MTC]在治疗前对第1组进行DURAMYCIN成像,并在治疗的第三天后进行24μl,通过动物单光子发射计算断层扫描(SPECT / CT)评估治疗响应。第2组小鼠连续处理10天,以观察肿瘤体积变化的治疗响应。通过TDT介导的DUTP缩乳末端标记(TUNEL)和切割的CASPASE-3(CC3)进一步证明治疗响应。结果[99MTC] MDA-MB-468肿瘤中的杜兰霉素摄取在治疗组中显着高于对照组,如3?天顺序处理(P?= 0.0001),治疗后也增加在治疗前(p?= 0.0001)。此外,[99MTC] Duramycin在肿瘤中摄取明显与免疫组织化学结果相关(Tunel:R?= 0.892,P?= 0.0001和CC3:R?= 0.89,P?= 0.0001)。此外,在治疗后第八天未观察到肿瘤大小减少,表明有效治疗,直到第八天,远远晚于诊断可以通过[99MTC] DURAMYCIN成像。结论[99MTC] Duramycin Spect / CT提供了化疗后早期检测肿瘤细胞凋亡的非侵入分子成像策略,因此在临床上可能具有很大的潜在价值。

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