Indiana Biosciences Research Institute, Indianapolis, IN 46202, USA.
Department of Radiology and Imaging Sciences, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Int J Mol Sci. 2020 Oct 1;21(19):7274. doi: 10.3390/ijms21197274.
There are presently no reliable ways to quantify human pancreatic beta cell mass (BCM) in vivo, which prevents an accurate understanding of the progressive beta cell loss in diabetes or following islet transplantation. Furthermore, the lack of beta cell imaging hampers the evaluation of the impact of new drugs aiming to prevent beta cell loss or to restore BCM in diabetes. We presently discuss the potential value of BCM determination as a cornerstone for individualized therapies in diabetes, describe the presently available probes for human BCM evaluation, and discuss our approach for the discovery of novel beta cell biomarkers, based on the determination of specific splice variants present in human beta cells. This has already led to the identification of DPP6 and FXYD2ga as two promising targets for human BCM imaging, and is followed by a discussion of potential safety issues, the role for radiochemistry in the improvement of BCM imaging, and concludes with an overview of the different steps from pre-clinical validation to a first-in-man trial for novel tracers.
目前尚无可靠的方法在体内定量人胰腺β细胞质量(BCM),这阻碍了对糖尿病或胰岛移植后β细胞进行性丧失的准确理解。此外,缺乏β细胞成像会阻碍评估旨在预防β细胞丢失或在糖尿病中恢复 BCM 的新药的影响。我们目前讨论了 BCM 测定作为糖尿病个体化治疗基石的潜在价值,描述了目前可用于评估人 BCM 的探针,并讨论了我们基于确定存在于人β细胞中的特定剪接变体来发现新型β细胞生物标志物的方法。这已经导致确定 DPP6 和 FXYD2ga 作为两种有前途的人 BCM 成像靶标,并随后讨论了潜在的安全问题、放射化学在改善 BCM 成像中的作用,并概述了从临床前验证到新型示踪剂首次人体试验的不同步骤。