2018
DOI: 10.20517/2394-4722.2017.78
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Circulating tumor cells in gastric cancer

Abstract: Circulating tumor cells (CTCs) have received a lot of attention as a novel biomarker for cancer research in past decades. CTCs infiltrate the bloodstream derived from the primary tumor, and are significantly involved in cancer metastasis and recurrence. Although clinical applications have been challenging owing to the difficulties of CTC identification, recent development of technology for specific enrichment and detection of CTCs contributes to diagnosis and treatment. Furthermore, CTC analyses will shed new … Show more

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Cited by 7 publications
(7 citation statements)
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“…Based on these findings, they speculated that the loss of TFF1 resulted in the epithelial-mesenchymal transition (EMT) of tumor cells and, therefore, upregulation of TFF1 might inhibit the EMT in cancer cells. During EMT, epithelial cells change their phenotype, exhibiting a reduction in cell-cell contacts, loss of polarity, increased cell motility and invasiveness, repression of epithelial cell markers (e.g., epithelial cells adhesion molecule (EpCAM), cytokeratin (CK), or E-cadherin), and aberrant upregulation of certain mesenchymal markers (e.g., vimentin and N-cadherin) [45]. Indeed, a recent study demonstrated that the overexpression of TFF1 inhibits EMT through regulation of TGF-β in gastric cancer cells.…”
Section: Discussionmentioning
confidence: 99%
“…Based on these findings, they speculated that the loss of TFF1 resulted in the epithelial-mesenchymal transition (EMT) of tumor cells and, therefore, upregulation of TFF1 might inhibit the EMT in cancer cells. During EMT, epithelial cells change their phenotype, exhibiting a reduction in cell-cell contacts, loss of polarity, increased cell motility and invasiveness, repression of epithelial cell markers (e.g., epithelial cells adhesion molecule (EpCAM), cytokeratin (CK), or E-cadherin), and aberrant upregulation of certain mesenchymal markers (e.g., vimentin and N-cadherin) [45]. Indeed, a recent study demonstrated that the overexpression of TFF1 inhibits EMT through regulation of TGF-β in gastric cancer cells.…”
Section: Discussionmentioning
confidence: 99%
“…CTCs are cancer cells that have been released either from the primary tumor site or from the metastatic sites [ 28 ]. Several meta-analyses have demonstrated an association between the presence of GC CTCs and advanced tumor stage, lymphatic invasion, and poorer survival [ 29 ]. There are various markers for gastric cancer CTCs; for the epithelial subtype, they include EpCAm, cytokeratin (CK): CK8, CK18, and CK19 and for the mesenchymal subtype, they include vimentin and twist [ 30 , 31 ].…”
Section: Diagnosismentioning
confidence: 99%
“…Currently used methods for CTC isolation include a primary step of enrichment consisting on depletion of red and white blood cells known as negative selection, and a positive selection based on their biological and physical properties, with subsequent identification supported by immunological, molecular, and functional markers. There are several enrichment technologies known, such as Cell Search, Adna Test, CTC-chip, MACS, or MagSweeper, all of them using epithelial cell adhesion molecule (EpCAM) as a surface marker for enrichment ( 8 ). The main issue is that during the metastasis process, involving migration, intravasation, circulation into the bloodstream, and extravasation with new organ colonization, CTCs undergo epithelial to mesenchymal transition (EMT) and lose their epithelial markers becoming more difficult to identify.…”
Section: Circulating Tumor Cells (Ctcs)mentioning
confidence: 99%