Dipartimento di Scienze e Tecnologie Biomediche, Università di Udine, Udine, Italy.
Clin Chem Lab Med. 2011 Feb;49(2):317-24. doi: 10.1515/CCLM.2011.060. Epub 2010 Dec 14.
The identification of reliable markers for diagnosis of breast cancer has been thoroughly addressed by metabolic profiling using nuclear magnetic resonance (NMR) spectroscopy or imaging. Several clear diagnostic indicators have emerged using either in vitro analysis of tissue extracts, ex vivo analysis of biopsies or in vivo direct spectral observations. Most of the breast cancer characteristic metabolites could be assayed by mass spectrometry (MS) to exploit the superior sensitivity of this technique and therefore reduce the traumatic impact of current biopsy procedures.
Following extraction, aqueous metabolite mixtures were obtained that were submitted to liquid-chromatography, electrospray-ionization, mass spectrometry (LC/ESI-MS) analysis to estimate the content of choline (Cho) and its phosphorylated derivatives, phosphocholine (PCho) and glycerophosphocholine (GPCho). The determinations were performed using 10 samples from breast tissue biopsies, surgical specimens and one single sample of a hepatic metastasis. In addition, some measurements were also repeated using high-resolution ¹H NMR spectroscopy to complement the mass spectrometry results.
The contents of Cho, PCho and GPCho in breast tissue extracts were estimated by LC/ESI-MS based on standard compound calibration curves. Sharply increased ratios of phosphorylated-to-unphosphorylated metabolites, PCho/ Cho and (PCho+GPCho)/Cho, were observed in all tumor samples, although without discrimination between benign and malignant lesions, contrary to samples from healthy individuals and from those with fibrocystic disease.
The assessment of breast cancer markers by LC/ESI-MS is feasible and diagnostically valuable. In addition to high sensitivity, the approach also shows a resolution advantage for assaying choline derivatives compared to NMR, and could complement the latter.
利用核磁共振(NMR)光谱或成像的代谢组学已经彻底研究了用于诊断乳腺癌的可靠标志物的鉴定。使用组织提取物的体外分析、活检的离体分析或体内直接光谱观察,已经出现了几个明确的诊断指标。通过质谱(MS)可以测定大多数乳腺癌特征代谢物,以利用该技术的超高灵敏度,从而减少当前活检程序的创伤性影响。
提取后获得水相代谢混合物,然后进行液相色谱、电喷雾电离、质谱(LC/ESI-MS)分析,以估计胆碱(Cho)及其磷酸化衍生物磷酸胆碱(PCho)和甘油磷酸胆碱(GPCho)的含量。使用 10 个来自乳腺组织活检、手术标本和一个肝转移的单一样本的样本进行测定。此外,还使用高分辨率 1H NMR 光谱进行了一些重复测量,以补充质谱结果。
通过基于标准化合物校准曲线的 LC/ESI-MS 估计了乳腺组织提取物中 Cho、PCho 和 GPCho 的含量。在所有肿瘤样本中,观察到磷酸化代谢物与非磷酸化代谢物的比值(PCho/Cho 和(PCho+GPCho)/Cho)急剧增加,尽管不能区分良性和恶性病变,与健康个体和纤维囊性疾病的样本不同。
LC/ESI-MS 评估乳腺癌标志物是可行的,具有诊断价值。该方法除了具有高灵敏度外,与 NMR 相比,在测定胆碱衍生物方面还具有分辨率优势,并可以补充后者。