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采用多阶谐波检测的电子顺磁共振成功实现了体内细胞外 pH 值的映射。

Electron Paramagnetic Resonance Implemented with Multiple Harmonic Detections Successfully Maps Extracellular pH In Vivo.

机构信息

Division of Bioengineering and Bioinformatics, Graduate School of Information Science and Technology, Hokkaido University, North 14, West 9, Kita-ku, Sapporo060-0814, Japan.

Laboratory of Radiation Biology, Graduate School of Veterinary Medicine, Hokkaido University, North 18, West 9, Kita-ku, Sapporo060-0818, Japan.

出版信息

Anal Chem. 2023 Feb 28;95(8):3940-3950. doi: 10.1021/acs.analchem.2c03194. Epub 2023 Feb 1.

Abstract

Extracellular acidification indicates a metabolic shift in cancer cells and is, along with tissue hypoxia, a hallmark of tumor malignancy. Thus, non-invasive mapping of extracellular pH (pHe) is essential for researchers to understand the tumor microenvironment and to monitor tumor response to metabolism-targeting drugs. While electron paramagnetic resonance (EPR) has been successfully used to map pHe in mouse xenograft models, this method is not sensitive enough to map pHe with a moderate amount of exogenous pH-sensitive probes. Here, we show that a modified EPR system achieves twofold higher sensitivity by using the multiple harmonic detection (MHD) method and improves the robustness of pHe mapping in mouse xenograft models. Our results demonstrate that treatment of a mouse xenograft model of human-derived pancreatic ductal adenocarcinoma cells with the carbonic anhydrase IX (CAIX) inhibitor U-104 delays tumor growth with a concurrent tendency toward further extracellular acidification. We anticipate that EPR-based pHe mapping can be expanded to monitor the response of other metabolism-targeting drugs. Furthermore, pHe monitoring can also be used for the development of improved metabolism-targeting cancer treatments.

摘要

细胞外酸化表明癌细胞发生代谢转变,并且与组织缺氧一起,是肿瘤恶性的标志。因此,非侵入性的细胞外 pH 值 (pHe) 测绘对于研究人员了解肿瘤微环境以及监测肿瘤对代谢靶向药物的反应至关重要。虽然电子顺磁共振 (EPR) 已成功用于在小鼠异种移植模型中测绘 pHe,但该方法的灵敏度不够高,无法使用适量的外源 pH 敏感探针测绘 pHe。在这里,我们展示了一种改良的 EPR 系统通过使用多次谐波检测 (MHD) 方法实现了两倍的灵敏度提高,并提高了在小鼠异种移植模型中 pHe 测绘的稳健性。我们的结果表明,用碳酸酐酶 IX (CAIX) 抑制剂 U-104 处理人源性胰腺导管腺癌细胞的小鼠异种移植模型可延迟肿瘤生长,同时伴有进一步的细胞外酸化趋势。我们预计,基于 EPR 的 pHe 测绘可扩展用于监测其他代谢靶向药物的反应。此外,pHe 监测还可用于开发改进的代谢靶向癌症治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/085f/9979135/33b040fb3547/ac2c03194_0002.jpg

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