Quantifying the Epithelial-to-Mesenchymal Transition (EMT) from Bench to Bedside

被引:26
作者
Brown, Meredith S. [1 ]
Muller, Kristen E. [2 ]
Pattabiraman, Diwakar R. [1 ,3 ]
机构
[1] Geisel Sch Med Dartmouth, Dept Mol & Syst Biol, Hanover, NH 03755 USA
[2] Dartmouth Hitchcock Med Ctr, Dept Pathol, Lebanon, NH 03756 USA
[3] Dartmouth Hitchcock Med Ctr, Norris Cotton Canc Ctr, Lebanon, NH 03756 USA
基金
美国国家卫生研究院;
关键词
epithelial-mesenchymal transition; EMT score; tumor heterogeneity; multiplexed immunofluorescence; CIRCULATING TUMOR-CELLS; BREAST-CANCER; E-CADHERIN; GENE-EXPRESSION; IN-VIVO; METASTASIS; SURVIVAL; REPRESSION; PLASTICITY; PROSTATE;
D O I
10.3390/cancers14051138
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The epithelial-to-mesenchymal transition (EMT) and its reversal, the mesenchymal-to-epithelial transition (MET) are critical components of the metastatic cascade in breast cancer and many other solid tumor types. Recent work has uncovered the presence of a variety of states encompassed within the EMT spectrum, each of which may play unique roles or work collectively to impact tumor progression. However, defining EMT status is not routinely carried out to determine patient prognosis or dictate therapeutic decision-making in the clinic. Identifying and quantifying the presence of various EMT states within a tumor is a critical first step to scoring patient tumors to aid in determining prognosis. Here, we review the major strides taken towards translating our understanding of EMT biology from bench to bedside. We review previously used approaches including basic immunofluorescence staining, flow cytometry, single-cell sequencing, and multiplexed tumor mapping. Future studies will benefit from the consideration of multiple methods and combinations of markers in designing a diagnostic tool for detecting and measuring EMT in patient tumors.
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页数:13
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