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首页> 外文期刊>Proteomics >Detection of molecular signatures of oral squamous cell carcinoma and normal epithelium - application of a novel methodology for unsupervised segmentation of imaging mass spectrometry data
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Detection of molecular signatures of oral squamous cell carcinoma and normal epithelium - application of a novel methodology for unsupervised segmentation of imaging mass spectrometry data

机译:口腔鳞状细胞癌和正常上皮细胞的分子特征检测-新型方法在质谱数据无监督分割中的应用

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Intra-tumor heterogeneity is a vivid problem of molecular oncology that could be addressed by imaging mass spectrometry. Here we aimed to assess molecular heterogeneity of oral squamous cell carcinoma and to detect signatures discriminating normal and cancerous epithelium. Tryptic peptides were analyzed by MALDI-IMS in tissue specimens from five patients with oral cancer. Novel algorithm of IMS data analysis was developed and implemented, which included Gaussian mixture modeling for detection of spectral components and iterative k-means algorithm for unsupervised spectra clustering performed in domain reduced to a subset of the most dispersed components. About 4% of the detected peptides showed significantly different abundances between normal epithelium and tumor, and could be considered as a molecular signature of oral cancer. Moreover, unsupervised clustering revealed two major sub-regions within expert-defined tumor areas. One of them showed molecular similarity with histologically normal epithelium. The other one showed similarity with connective tissue, yet was markedly different from normal epithelium. Pathologist's re-inspection of tissue specimens confirmed distinct features in both tumor sub-regions: foci of actual cancer cells or cancer microenvironment-related cells prevailed in corresponding areas. Hence, molecular differences detected during automated segmentation of IMS data had an apparent reflection in real structures present in tumor.
机译:肿瘤内异质性是分子肿瘤学中一个生动的问题,可以通过成像质谱法解决。在这里,我们旨在评估口腔鳞状细胞癌的分子异质性,并检测区分正常和癌性上皮的特征。通过MALDI-IMS对五名口腔癌患者的组织样本中的胰蛋白酶解肽进行了分析。开发并实施了IMS数据分析的新算法,其中包括用于光谱成分检测的高斯混合模型和用于在域中进行的非监督光谱聚类的迭代k均值算法,该算法被简化为最分散的成分的子集。大约4%的检测到的肽在正常上皮和肿瘤之间显示出明显不同的丰度,可以被认为是口腔癌的分子特征。此外,无监督的聚类揭示了专家定义的肿瘤区域内的两个主要子区域。其中之一显示与组织学上正常的上皮分子相似。另一个与结缔组织相似,但与正常上皮明显不同。病理学家对组织标本的重新检查证实了这两个肿瘤亚区域的明显特征:实际癌细胞或与癌症微环境相关的细胞的病灶在相应的区域盛行。因此,在IMS数据的自动分割过程中检测到的分子差异在肿瘤中存在的真实结构中有明显的反映。

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