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Validation of Breast Cancer Margins by Tissue Spray Mass Spectrometry

机译:组织喷雾质谱验证乳腺癌边缘

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Current methods for the intraoperative determination of breast cancer margins commonly suffer from the insufficient accuracy, specificity and/or low speed of analysis, increasing the time and cost of operation as well the risk of cancer recurrence. The purpose of this study is to develop a method for the rapid and accurate determination of breast cancer margins using direct molecular profiling by mass spectrometry (MS). Direct molecular fingerprinting of tiny pieces of breast tissue (approximately 1 × 1 × 1 mm) is performed using a home-built tissue spray ionization source installed on a Maxis Impact quadrupole time-of-flight mass spectrometer (qTOF MS) (Bruker Daltonics, Hamburg, Germany). Statistical analysis of MS data from 50 samples of both normal and cancer tissue (from 25 patients) was performed using orthogonal projections onto latent structures discriminant analysis (OPLS-DA). Additionally, the results of OPLS classification of new 19 pieces of two tissue samples were compared with the results of histological analysis performed on the same tissues samples. The average time of analysis for one sample was about 5 min. Positive and negative ionization modes are used to provide complementary information and to find out the most informative method for a breast tissue classification. The analysis provides information on 11 lipid classes. OPLS-DA models are created for the classification of normal and cancer tissue based on the various datasets: All mass spectrometric peaks over 300 counts; peaks with a statistically significant difference of intensity determined by the Mann–Whitney U-test ( p 0.05); peaks identified as lipids; both identified and significantly different peaks. The highest values of Q2 have models built on all MS peaks and on significantly different peaks. While such models are useful for classification itself, they are of less value for building explanatory mechanisms of pathophysiology and providing a pathway analysis. Models based on identified peaks are preferable from this point of view. Results obtained by OPLS-DA classification of the tissue spray MS data of a new sample set ( n = 19) revealed 100% sensitivity and specificity when compared to histological analysis, the “gold” standard for tissue classification. “All peaks” and “significantly different peaks” datasets in the positive ion mode were ideal for breast cancer tissue classification. Our results indicate the potential of tissue spray mass spectrometry for rapid, accurate and intraoperative diagnostics of breast cancer tissue as a means to reduce surgical intervention.
机译:目前用于术中测定乳腺癌边缘的方法通常患有不足的准确性,特异性和/或低分析速度,增加了癌症复发风险的时间和成本。本研究的目的是开发一种用于快速准确地测定使用质谱(MS)的直接分子分析的乳腺癌利润的方法。使用安装在Maxis冲击Quadrupole飞行时间质谱仪(QTOF MS)的自制组织喷雾电离源(QTOF)(Bruker Daltonics)的自制组织喷涂电离源进行直接分子指纹汉堡,德国)。使用正交突起在潜在结构判别分析(OPLS-DA)上进行来自正常和癌组织的50个样本的MS数据的统计分析来自正常和癌症组织的50个样本(来自25例)。另外,与在同一组织样品上进行的组织学分析的结果进行比较新的19种组织样本的OPLS分类的结果。一个样品的平均分析时间约为5分钟。正极和负电离模式用于提供互补信息,并找出乳房组织分类的最具信息性方法。分析提供了有关11个脂质类的信息。根据各种数据集创建OPLS-DA模型,用于基于各种数据集:所有质谱峰值超过300计数;峰值具有统计上显着的强度差异,由Mann-Whitney U-Test确定(P <0.05);峰被鉴定为脂质;两者都识别和显着不同的峰。 Q2的最高值具有构建在所有MS峰上的型号,并且在显着不同的峰值上。虽然这种模型对于分类本身是有用的,但它们的价值较低,用于构建病理生理学的解释机制并提供途径分析。从该观点来看,基于所识别的峰值的模型是优选的。由OPLS-DA分类获得的新样品组的组织喷射MS数据(n = 19)获得的结果显示,与组织学分析相比,增加了100%的敏感性和特异性,“黄金”组织分类标准。正离子模式中的“所有峰”和“显着不同的峰值”数据集是乳腺癌组织分类的理想选择。我们的结果表明组织喷雾质谱的潜力,用于乳腺癌组织的快速,准确和术目不然诊断,作为减少手术干预的手段。

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