Mills P, Buonomo C, Pillai R P, Samphilipo M A, Rajan S S, Strandberg J D, Anderson J H
Department of Radiology and Radiological Science, Johns Hopkins Medical Institutions, Baltimore, Maryland.
Invest Radiol. 1988 Aug;23(8):584-91. doi: 10.1097/00004424-198808000-00008.
In vivo and in vitro 31P-NMR spectroscopy was used to study the high energy phosphate metabolism of VX-2 tumors implanted into rabbit liver, kidney, and hind-limb muscle. Tumors, at various stages of growth, were first examined by in vivo 31P-NMR spectroscopy, then they were excised and underwent histologic examination and biochemical analysis; both in vitro 31P-NMR and standard enzymatic techniques were used. There was good correlation among the in vivo NMR spectra, the in vitro NMR data, and the biochemical analyses. Although the tumor spectra showed characteristics similar to those reported in the other tumor models, there was a striking variability in the spectra obtained from tumors implanted in the same site and from different sites. There was poor correlation between the degree of necrosis in the tumor and the tumor pH and between the Pi:ATP ratio and necrosis. This variability has important implications for the potential value of using 31P-NMR spectroscopy to monitor tumor growth and therapy in vivo.
采用体内和体外31P-NMR光谱法研究接种于兔肝脏、肾脏和后肢肌肉的VX-2肿瘤的高能磷酸代谢。首先通过体内31P-NMR光谱法检查处于不同生长阶段的肿瘤,然后将其切除并进行组织学检查和生化分析;同时采用体外31P-NMR和标准酶学技术。体内NMR光谱、体外NMR数据和生化分析之间具有良好的相关性。虽然肿瘤光谱显示出与其他肿瘤模型报道的特征相似,但从同一部位和不同部位接种的肿瘤获得的光谱存在显著差异。肿瘤坏死程度与肿瘤pH值之间以及Pi:ATP比值与坏死之间的相关性较差。这种变异性对于利用31P-NMR光谱法在体内监测肿瘤生长和治疗的潜在价值具有重要意义。