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[F]-SuPAR:一种用于非侵入性成像 DNA 损伤依赖性聚(ADP-核糖)聚合酶活性的放射性氟探针。

[F]-SuPAR: A Radiofluorinated Probe for Noninvasive Imaging of DNA Damage-Dependent Poly(ADP-ribose) Polymerase Activity.

出版信息

Bioconjug Chem. 2019 May 15;30(5):1331-1342. doi: 10.1021/acs.bioconjchem.9b00089. Epub 2019 Apr 22.

Abstract

Poly(ADP ribose) polymerase (PARP) enzymes generate poly(ADP ribose) post-translational modifications on target proteins for an array of functions centering on DNA and cell stress. PARP isoforms 1 and 2 are critically charged with the surveillance of DNA integrity and are the first line guardians of the genome against DNA breaks. Here we present a novel probe ([F]-SuPAR) for noninvasive imaging of PARP-1/2 activity using positron emission tomography (PET). [F]-SuPAR is a radiofluorinated nicotinamide adenine dinucleotide (NAD) analog that can be recognized by PARP-1/2 and incorporated into the long branched polymers of poly(ADP ribose) (PAR). The measurement of PARP-1/2 activity was supported by a reduction of radiotracer uptake in vivo following PARP-1/2 inhibition with talazoparib treatment, a potent PARP inhibitor recently approved by FDA for treatment of breast cancer, as well as ex vivo colocalization of radiotracer analog and poly(ADP ribose). With [F]-SuPAR, we were able to map the dose- and time-dependent activation of PARP-1/2 following radiation therapy in breast and cervical cancer xenograft mouse models. Tumor response to therapy was determined by [F]-SuPAR PET within 8 h of administration of a single dose of radiation equivalent to one round of stereotactic ablative radiotherapy.

摘要

聚(ADP 核糖)聚合酶(PARP)酶在靶蛋白上生成聚(ADP 核糖)翻译后修饰,用于一系列以 DNA 和细胞应激为中心的功能。PARP 同工型 1 和 2 负责监控 DNA 完整性,是基因组抵御 DNA 断裂的第一道防线。在这里,我们提出了一种新的探针([F]-SuPAR),用于使用正电子发射断层扫描(PET)进行 PARP-1/2 活性的非侵入性成像。[F]-SuPAR 是一种放射性标记的烟酰胺腺嘌呤二核苷酸(NAD)类似物,可以被 PARP-1/2 识别并掺入聚(ADP 核糖)(PAR)的长支链聚合物中。PARP-1/2 活性的测量得到了以下支持:用 PARP 抑制剂 talazoparib 处理后,体内放射性示踪剂摄取减少,PARP-1/2 抑制剂最近获得 FDA 批准用于治疗乳腺癌,以及放射性示踪剂类似物和聚(ADP 核糖)的体外共定位。使用 [F]-SuPAR,我们能够在乳腺癌和宫颈癌异种移植小鼠模型中绘制放射治疗后 PARP-1/2 的剂量和时间依赖性激活图。通过单次辐射剂量给药后 8 小时内的 [F]-SuPAR PET 来确定肿瘤对治疗的反应,该剂量相当于一轮立体定向消融放疗。

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