Department of Surgery and Cancer, Imperial College, London, UK.
Eur J Cancer. 2012 Mar;48(4):432-40. doi: 10.1016/j.ejca.2011.11.033. Epub 2012 Jan 5.
The capacity to evade apoptosis has been defined as one of the hallmarks of cancer and, thus, effective anti-cancer therapy often induces apoptosis. A biomarker for imaging apoptosis could assist in monitoring the efficacy of a wide range of current and future therapeutics. Despite the potential, there are limited clinical examples of the use of positron emission tomography for imaging of apoptosis. [(18)F]ICMT-11 is a novel reagent designed to non-invasively image caspase-3 activation and, hence, drug-induced apoptosis. Radiochemistry development of [(18)F]ICMT-11 has been undertaken to improve specific radioactivity, reduce content of stable impurities, reduce synthesis time and enable automation for manufacture of multi-patient dose. Due to the promising mechanistic and safety profile of [(18)F]ICMT-11, the radiotracer is transitioning to clinical development and has been selected as a candidate radiotracer by the QuIC-ConCePT consortium for further evaluation in preclinical models and humans. A successful outcome will allow use of the radiotracer as qualified method for evaluating the pharmaceutical industry's next generation therapeutics.
逃避细胞凋亡的能力已被定义为癌症的标志之一,因此,有效的抗癌疗法通常会诱导细胞凋亡。用于成像细胞凋亡的生物标志物可以帮助监测当前和未来广泛治疗方法的疗效。尽管有这种潜力,但使用正电子发射断层扫描术 (PET) 进行细胞凋亡成像的临床应用例子有限。[(18)F]ICMT-11 是一种新型试剂,旨在非侵入性地成像半胱氨酸蛋白酶-3 的激活,从而成像药物诱导的细胞凋亡。[(18)F]ICMT-11 的放射化学开发旨在提高比活度、降低稳定杂质的含量、缩短合成时间,并实现多患者剂量的自动化生产。由于 [(18)F]ICMT-11 的机制和安全性特征很有前景,该示踪剂正在向临床开发阶段过渡,并已被 QuIC-ConCePT 联盟选为候选示踪剂,以在临床前模型和人体中进行进一步评估。如果成功,该示踪剂将可被用于评估制药行业下一代疗法的合格方法。