Detour Julien, Pierre Alice, Boisson Fréderic, Kreutter Guillaume, Lavaux Thomas, Namer Izzie Jacques, Kessler Laurence, Brasse David, Marchand Patrice, Imperiale Alessio
Department of Radiopharmacy, Strasbourg University Hospitals, Strasbourg, France.
Department of Biophysics and Nuclear Medicine, Strasbourg University Hospitals, Strasbourg, France.
J Nucl Med. 2017 Jan;58(1):36-41. doi: 10.2967/jnumed.116.180588. Epub 2016 Sep 8.
Patient premedication with carbidopa seems to improve the accuracy of 6-F-fluoro-3,4-dihydroxy-l-phenylalanine (F-FDOPA) PET for insulinoma diagnosis. However, the risk of PET false-negative results in the presence of carbidopa is a concern. Consequently, we aimed to evaluate the effect of carbidopa on F-FDOPA uptake in insulinoma β-cells and an insulinoma xenograft model in mice.
F-FDOPA in vitro accumulation was assessed in the murine β-cell line RIN-m5F. In vivo small-animal PET experiments were performed on tumor-bearing nude mice after subcutaneous injection of RIN-m5F cells. Experiments were conducted with and without carbidopa pretreatment.
Incubation of RIN-m5F cells with 80 μM carbidopa did not significantly affect the cellular accumulation of F-FDOPA. Tumor xenografts were clearly detectable by small-animal PET in all cases. Insulinoma xenografts in carbidopa-treated mice showed significantly higher F-FDOPA uptake than those in nontreated mice. Regardless of carbidopa premedication, the xenografts were characterized by an early increase in F-FDOPA uptake and then a progressive reduction over time.
Carbidopa did not influence in vitro F-FDOPA accumulation in RIN-m5F cells but improved insulinoma imaging in vivo. Our findings increase current knowledge about the F-FDOPA uptake profile of RIN-m5F cells and a related xenograft model. To our knowledge, the present work represents the first preclinical research specifically focused on insulinomas, with potential translational implications.
使用卡比多巴对患者进行术前用药似乎可提高6-F-氟-3,4-二羟基-L-苯丙氨酸(F-FDOPA)PET诊断胰岛素瘤的准确性。然而,在使用卡比多巴的情况下PET出现假阴性结果的风险令人担忧。因此,我们旨在评估卡比多巴对胰岛素瘤β细胞和小鼠胰岛素瘤异种移植模型中F-FDOPA摄取的影响。
在小鼠β细胞系RIN-m5F中评估F-FDOPA的体外积累。对皮下注射RIN-m5F细胞的荷瘤裸鼠进行体内小动物PET实验。实验在有或没有卡比多巴预处理的情况下进行。
用80μM卡比多巴孵育RIN-m5F细胞对F-FDOPA的细胞积累没有显著影响。在所有情况下,小动物PET均可清晰检测到肿瘤异种移植。卡比多巴治疗的小鼠中的胰岛素瘤异种移植显示出比未治疗小鼠更高的F-FDOPA摄取。无论是否进行卡比多巴术前用药,异种移植的特征都是F-FDOPA摄取早期增加,然后随时间逐渐减少。
卡比多巴不影响RIN-m5F细胞中F-FDOPA的体外积累,但可改善体内胰岛素瘤成像。我们的发现增加了目前关于RIN-m5F细胞和相关异种移植模型的F-FDOPA摄取情况的知识。据我们所知,目前的工作代表了第一项专门针对胰岛素瘤的临床前研究,具有潜在的转化意义。