Einoch Amor Reef, Levy Jeremy, Broza Yoav Y, Vangravs Reinis, Rapoport Shelley, Zhang Min, Wu Weiwei, Leja Marcis, Behar Joachim A, Haick Hossam
Department of Chemical Engineering and Russell Berrie Nanotechnology Institute, Technion-Israel Institute of Technology, Haifa 3200003, Israel.
The Andrew and Erna Viterbi Faculty of Electrical & Computer Engineering and Faculty of Biomedical Engineering, Technion-Israel Institute of Technology, Haifa 3200003, Israel.
ACS Sens. 2023 Apr 28;8(4):1450-1461. doi: 10.1021/acssensors.2c02422. Epub 2023 Mar 16.
Liquid biopsy is seen as a prospective tool for cancer screening and tracking. However, the difficulty lies in effectively sieving, isolating, and overseeing cancer biomarkers from the backdrop of multiple disrupting cells and substances. The current study reports on the ability to perform liquid biopsy without the need to physically filter and/or isolate the cancer cells per se. This has been achieved through the detection and classification of volatile organic compounds (VOCs) emitted from the cancer cells found in the headspace of blood or urine samples or a combined data set of both. Spectrometric analysis shows that blood and urine contain complementary or overlapping VOC information on kidney cancer, gastric cancer, lung cancer, and fibrogastroscopy subjects. Based on this information, a nanomaterial-based chemical sensor array in conjugation with machine learning as well as data fusion of the signals achieved was carried out on various body fluids to assess the VOC profiles of cancer. The detection of VOC patterns by either Gas Chromatography-Mass Spectrometry (GC-MS) analysis or our sensor array achieved >90% accuracy, >80% sensitivity, and >80% specificity in different binary classification tasks. The hybrid approach, namely, analyzing the VOC datasets of blood and urine together, contributes an additional discrimination ability to the improvement (>3%) of the model's accuracy. The contribution of the hybrid approach for an additional discrimination ability to the improvement of the model's accuracy is examined and reported.
液体活检被视为癌症筛查和跟踪的一种前瞻性工具。然而,困难在于如何在多种干扰细胞和物质的背景下有效地筛选、分离和监测癌症生物标志物。当前的研究报告了一种无需对癌细胞进行物理过滤和/或分离就能进行液体活检的能力。这是通过检测和分类血液或尿液样本顶空中发现的癌细胞所释放的挥发性有机化合物(VOCs)或两者的组合数据集来实现的。光谱分析表明,血液和尿液包含关于肾癌、胃癌、肺癌和纤维胃镜检查对象的互补或重叠的VOC信息。基于此信息,在各种体液上进行了结合机器学习的基于纳米材料的化学传感器阵列以及所获得信号的数据融合,以评估癌症的VOC谱。通过气相色谱-质谱(GC-MS)分析或我们的传感器阵列检测VOC模式,在不同的二元分类任务中实现了>90%的准确率、>80%的灵敏度和>80%的特异性。混合方法,即一起分析血液和尿液的VOC数据集,为提高模型的准确率(>3%)贡献了额外的辨别能力。本文对混合方法为提高模型准确率贡献额外辨别能力进行了研究和报告。