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细胞周期蛋白依赖性激酶4/6抑制剂的镓-68标记作为用于肿瘤成像的正电子发射断层显像放射性示踪剂

Gallium-68 Labeling of the Cyclin-Dependent Kinase 4/6 Inhibitors as Positron Emission Tomography Radiotracers for Tumor Imaging.

作者信息

Liu Cheng, Yang Ziyi, Liu Mingyu, Wang Xiangwei, Song Shaoli, Xu Xiaoping, Yang Zhongyi

机构信息

Department of Nuclear Medicine, Fudan University Shanghai Cancer Center, Shanghai 200032, China.

Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China.

出版信息

ACS Omega. 2021 Nov 18;6(47):32253-32261. doi: 10.1021/acsomega.1c05073. eCollection 2021 Nov 30.

Abstract

Cyclin-dependent kinase 4 and 6 (CDK4/6) have emerged as interesting therapeutic drug targets with many potential applications in anti-tumors, especially in breast cancer. A novel CDK4/6 kinase-derived positron emission tomography (PET) imaging agent was designed based on palbociclib modified with a chelator DOTA. This new compound with a chelator DOTA-palbociclib was radiolabeled with gallium 68 (Ga). After labeling, the purity and stability were evaluated, and the blood pharmacokinetics were carried out in normal healthy mice. Human breast cancer MCF-7 (ER+/HER2-) cells were used for cell uptake tests. PET imaging and biodistribution were conducted in MCF-7 tumor-bearing mice. Specific binding of tumors was evaluated by the blocking assay. Furthermore, the uptake of Ga-DOTA-palbociclib in tumors was studied by autoradiography of tissue sections followed by immunofluorescence evaluation of CDK4 and CDK6. Ga-DOTA-palbociclib was synthesized very simply in a high labeling rate and radiochemical purity in 10 min. The labeling compound showed excellent stability both and and exhibited good pharmacokinetics, making it suitable for imaging. Cell uptake studies display that co-incubation with palbociclib can inhibit cellular uptake of Ga-DOTA-palbociclib. imaging and biodistribution in mice bearing MCF-7 tumors both showed obvious radioactive uptake in the tumor and higher tumor-to-muscle ratios, while the tumor radioactivity accumulation was significantly decreased when prior administered with an excess of cold palbociclib, confirming CDK4/6 specific binding of Ga-DOTA-palbociclib . Autoradiography of the avid tumor section showed a high correlation between immunofluorescence with the CDK4/6 positive areas of the tumor, further demonstrating that Ga-DOTA-palbociclib specifically targeted CDK4/6 positive tumors. We synthesized Ga-DOTA-palbociclib, a new CDK4/6 kinase PET imaging agent, and validated its excellent stability, pharmacokinetics, and specific tumor binding. Based on our primary results, Ga-DOTA-palbociclib is a promising imaging agent with the potential to tailor a precise treatment program for CDK4/6 inhibitors.

摘要

细胞周期蛋白依赖性激酶4和6(CDK4/6)已成为有趣的治疗药物靶点,在抗肿瘤尤其是乳腺癌方面有许多潜在应用。基于用螯合剂DOTA修饰的帕博西尼设计了一种新型的CDK4/6激酶衍生的正电子发射断层扫描(PET)显像剂。这种带有螯合剂DOTA - 帕博西尼的新化合物用镓68(Ga)进行放射性标记。标记后,评估其纯度和稳定性,并在正常健康小鼠中进行血液药代动力学研究。用人乳腺癌MCF - 7(ER + /HER2 - )细胞进行细胞摄取试验。在荷MCF - 7肿瘤的小鼠中进行PET成像和生物分布研究。通过阻断试验评估肿瘤的特异性结合。此外,通过组织切片放射自显影,随后对CDK4和CDK6进行免疫荧光评估,研究了Ga - DOTA - 帕博西尼在肿瘤中的摄取情况。Ga - DOTA - 帕博西尼在10分钟内以高标记率和放射化学纯度非常简单地合成。标记化合物在体外和体内均显示出优异的稳定性,并表现出良好的药代动力学,使其适用于成像。细胞摄取研究表明,与帕博西尼共同孵育可抑制Ga - DOTA - 帕博西尼的细胞摄取。在荷MCF - 7肿瘤小鼠中的成像和生物分布均显示肿瘤中有明显的放射性摄取,且肿瘤与肌肉的比值更高,而预先给予过量的冷帕博西尼时,肿瘤放射性积累显著降低,证实了Ga - DOTA - 帕博西尼与CDK4/6的特异性结合。肿瘤切片的放射自显影显示与肿瘤CDK4/6阳性区域的免疫荧光之间有高度相关性,进一步证明Ga - DOTA - 帕博西尼特异性靶向CDK4/6阳性肿瘤。我们合成了新型CDK4/6激酶PET显像剂Ga - DOTA - 帕博西尼,并验证了其优异的稳定性、药代动力学和肿瘤特异性结合。基于我们的初步结果,Ga - DOTA - 帕博西尼是一种有前景的显像剂,有潜力为CDK4/6抑制剂量身定制精确的治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a5c/8638300/5897abd4cb92/ao1c05073_0002.jpg

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