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使用PARP1靶向光学成像剂检测和描绘口腔癌

Detection and Delineation of Oral Cancer With a PARP1-Targeted Optical Imaging Agent.

作者信息

Kossatz Susanne, Weber Wolfgang, Reiner Thomas

机构信息

1 Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

2 Molecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

出版信息

Mol Imaging. 2017 Jan-Dec;16:1536012117723786. doi: 10.1177/1536012117723786.

Abstract

More sensitive and specific methods for early detection are imperative to improve survival rates in oral cancer. However, oral cancer detection is still largely based on visual examination and histopathology of biopsy material, offering no molecular selectivity or spatial resolution. Intuitively, the addition of optical contrast could improve oral cancer detection and delineation, but so far no molecularly targeted approach has been translated. Our fluorescently labeled small-molecule inhibitor PARPi-FL binds to the DNA repair enzyme poly(ADP-ribose)polymerase 1 (PARP1) and is a potential diagnostic aid for oral cancer delineation. Based on our preclinical work, a clinical phase I/II trial opened in March 2017 to evaluate PARPi-FL as a contrast agent for oral cancer imaging. In this commentary, we discuss why we chose PARP1 as a biomarker for tumor detection and which particular characteristics make PARPi-FL an excellent candidate to image PARP1 in optically guided applications. We also comment on the potential benefits of our molecularly targeted PARPi-FL-guided imaging approach in comparison to existing oral cancer screening adjuncts and mention the adaptability of PARPi-FL imaging to other environments and tumor types.

摘要

早期检测的更灵敏、更具特异性的方法对于提高口腔癌的生存率至关重要。然而,口腔癌检测在很大程度上仍基于活检材料的视觉检查和组织病理学,缺乏分子选择性或空间分辨率。直观地说,添加光学对比剂可以改善口腔癌的检测和轮廓描绘,但迄今为止尚未有分子靶向方法得以应用。我们的荧光标记小分子抑制剂PARPi-FL可与DNA修复酶聚(ADP-核糖)聚合酶1(PARP1)结合,是用于口腔癌轮廓描绘的潜在诊断辅助剂。基于我们的临床前研究工作,一项I/II期临床试验于2017年3月启动,以评估PARPi-FL作为口腔癌成像的对比剂。在这篇评论中,我们讨论了为何选择PARP1作为肿瘤检测的生物标志物,以及PARPi-FL在光学引导应用中成为PARP1成像的优秀候选物的特殊特性。我们还评论了与现有的口腔癌筛查辅助手段相比,我们的分子靶向PARPi-FL引导成像方法的潜在优势,并提及PARPi-FL成像对其他环境和肿瘤类型的适应性。

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