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对来自头颈部鳞状细胞癌患者的负富集血液样本进行多参数分析,包括 EMT 标志物。

Multiparameter analysis, including EMT markers, on negatively enriched blood samples from patients with squamous cell carcinoma of the head and neck.

机构信息

William G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, Ohio, United States of America.

出版信息

PLoS One. 2012;7(7):e42048. doi: 10.1371/journal.pone.0042048. Epub 2012 Jul 26.

Abstract

Epithelial to mesenchymal transition (EMT) has been hypothesized as a mechanism by which cells change phenotype during carcinogenesis, as well as tumor metastasis. Whether EMT is involved in cancer metastasis has a specific, practical impact on the field of circulating tumor cells (CTCs). Since the generally accepted definition of a CTC includes the expression of epithelial surface markers, such as EpCAM, if a cancer cell loses its epithelial surface markers (which is suggested in EMT), it will not be separated and/or identified as a CTC. We have developed, and previously reported on the use of, a purely negative enrichment technology enriching for CTCs in the blood of squamous cell carcinoma of the head and neck (SCCHN). This methodology does not depend on the expression of surface epithelial markers. Using this technology, our initial data on SCCHN patient blood indicates that the presence of CTCs correlates with worse disease-free survival. Since our enrichment is not dependent on epithelial markers, we have initiated investigation of the presence of mesenchymal markers in these CTC cells to include analysis of: vimentin, epidermal growth factor receptor, N-cadherin, and CD44. With the aid of confocal microscopy, we have demonstrated not only presumed CTCs that express and/or contain: a nucleus, cytokeratins, vimentin, and either EGFR, CD44, or N-cadherin, but also cells that contain all of the aforementioned proteins except cytokeratins, suggesting that the cells have undergone the EMT process. We suggest that our negative depletion enrichment methodology provides a more objective approach in identifying and evaluating CTCs, as opposed to positive selection approaches, as it is not subjective to a selection bias and can be tailored to accommodate a variety of cytoplasmic and surface markers which can be evaluated to identify a multitude of phenotypic patterns within CTCs from individual patients, including so-called EMT as presented here.

摘要

上皮-间充质转化 (EMT) 被认为是细胞在癌变过程中改变表型的机制,也是肿瘤转移的机制。EMT 是否参与癌症转移对循环肿瘤细胞 (CTC) 的领域有具体的、实际的影响。由于 CTC 的一般定义包括上皮表面标志物的表达,如 EpCAM,如果癌细胞失去上皮表面标志物(这在 EMT 中有所提示),它将不会被分离和/或识别为 CTC。我们已经开发并以前报告过使用纯粹的阴性富集技术在头颈部鳞状细胞癌 (SCCHN) 的血液中富集 CTC。这种方法不依赖于表面上皮标志物的表达。使用这项技术,我们最初在 SCCHN 患者血液中的数据表明,CTC 的存在与无病生存期更差相关。由于我们的富集不依赖于上皮标志物,我们已经开始研究这些 CTC 细胞中是否存在间充质标志物,包括分析波形蛋白、表皮生长因子受体、N-钙粘蛋白和 CD44。在共聚焦显微镜的帮助下,我们不仅证明了表达和/或含有:细胞核、细胞角蛋白、波形蛋白和 EGFR、CD44 或 N-钙粘蛋白的假定 CTC,还证明了含有除细胞角蛋白外所有上述蛋白的细胞,这表明这些细胞已经经历了 EMT 过程。我们认为,与阳性选择方法相比,我们的阴性耗尽富集方法在识别和评估 CTC 方面提供了一种更客观的方法,因为它不受选择偏见的影响,并且可以根据需要进行调整,以适应各种细胞质和表面标志物的评估,以识别来自个体患者的 CTC 中的多种表型模式,包括这里提出的所谓 EMT。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ccf/3406036/025e509034ab/pone.0042048.g001.jpg

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