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• W3000460221 abstract "ObjectiveRecent studies demonstrated that circulating tumor cells (CTCs) contribute to the metastasis of prostate cancer. Survivin knockout could inhibit epithelial-mesenchymal transition (EMT) and suppress several metastatic tumors. In this study, we examined the potential involvement of survivin in EMT in CTCs. MethodsCTCs were isolated from the peripheral blood of 100 patients with prostate cancer as EpCAM+/CD45− cells via FACS sorting and identified by immunofluorescence staining of prostate-specific antigen (PSA). CTCs and DU145 cells were transfected with survivin siRNA. Then, the levels of survivin, E-cadherin, and vimentin in CTCs and DU145 cells were detected via immunofluorescence staining, and the invasiveness of CTCs and DU145 cells was examined using a Transwell chamber. ResultsThe results revealed the abundant expression of PSA in the cytoplasm of CTCs. Transfection of survivin siRNA significantly decreased the levels of survivin and vimentin in CTCs and DU145, whereas that of E-cadherin was significantly increased, suggesting survivin plays an important role in EMT of CTCs. In addition, survivin siRNA significantly inhibited the invasiveness of CTCs and DU145 cells. ConclusionsSurvivin plays an important role in EMT of CTCs in prostate cancer, which might mediate the metastasis and invasion of prostate cancer." @default.
• W3000460221 created "2020-01-23" @default.
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• W3000460221 date "2020-01-01" @default.
• W3000460221 modified "2023-09-25" @default.
• W3000460221 title "Epithelial-mesenchymal transition of circulating tumor cells in prostate cancer is promoted by survivin" @default.
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• W3000460221 doi "https://doi.org/10.1177/0300060519892395" @default.
• W3000460221 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7254165" @default.
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