Martin Benedikt, Gonçalves Juliana P L, Bollwein Christine, Sommer Florian, Schenkirsch Gerhard, Jacob Anne, Seibert Armin, Weichert Wilko, Märkl Bruno, Schwamborn Kristina
Institute of Pathology and Molecular Tumor Diagnostics, University Hospital of Augsburg, 86156 Augsburg, Germany.
Institute of Pathology, School of Medicine, Technical University of Munich, 81675 Munich, Germany.
Cancers (Basel). 2021 Oct 26;13(21):5371. doi: 10.3390/cancers13215371.
Currently, pathological evaluation of stage I/II colon cancer, following the Union Internationale Contre Le Cancer (UICC) guidelines, is insufficient to identify patients that would benefit from adjuvant treatment. In our study, we analyzed tissue samples from 276 patients with colon cancer utilizing mass spectrometry imaging. Two distinct approaches are herein presented for data processing and analysis. In one approach, four different machine learning algorithms were applied to predict the tendency to develop metastasis, which yielded accuracies over 90% for three of the models. In the other approach, 1007 / features were evaluated with regards to their prognostic capabilities, yielding two / features as promising prognostic markers. One feature was identified as a fragment from collagen (collagen 3A1), hinting that a higher collagen content within the tumor is associated with poorer outcomes. Identification of proteins that reflect changes in the tumor and its microenvironment could give a very much-needed prediction of a patient's prognosis, and subsequently assist in the choice of a more adequate treatment.
目前,按照国际抗癌联盟(UICC)指南对I/II期结肠癌进行的病理评估,不足以识别出能从辅助治疗中获益的患者。在我们的研究中,我们利用质谱成像分析了276例结肠癌患者的组织样本。本文提出了两种不同的数据处理和分析方法。在一种方法中,应用了四种不同的机器学习算法来预测发生转移的倾向,其中三个模型的准确率超过了90%。在另一种方法中,对1007个特征的预后能力进行了评估,得出两个特征有望成为预后标志物。其中一个特征被鉴定为胶原蛋白(胶原蛋白3A1)的片段,这表明肿瘤内较高的胶原蛋白含量与较差的预后相关。识别反映肿瘤及其微环境变化的蛋白质,可以对患者的预后做出非常急需的预测,并随后有助于选择更合适的治疗方法。