| Literature DB >> 23845299 |
Rhonda L Bitting1, Rengasamy Boominathan, Chandra Rao, Gabor Kemeny, Brad Foulk, Mariano A Garcia-Blanco, Mark Connelly, Andrew J Armstrong.
Abstract
Epithelial tumor cells can become mesenchymal cells and vice versa via phenotypic transitions, a process known as epithelial plasticity. We postulate that during the process of metastasis, circulating tumor cells (CTCs) lose their epithelial phenotype and acquire a mesenchymal phenotype that may not be sufficiently captured by existing epithelial-based CTC technologies. We report here on the development of a novel CTC capture method, based on the biology of epithelial plasticity, which isolates cells based on OB-cadherin cell surface expression. Using this mesenchymal-based assay, OB-cadherin cellular events are detectable in men with metastatic prostate cancer and are less common in healthy volunteers. This method may complement existing epithelial-based methods and may be particularly useful in patients with bone metastases.Entities:
Keywords: Circulating tumor cells; Epithelial plasticity; Epithelial–mesenchymal transition; OB-cadherin; Osteomimicry; Prostate cancer
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Year: 2013 PMID: 23845299 PMCID: PMC3833983 DOI: 10.1016/j.ymeth.2013.06.034
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608