Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/96490
Citations
Scopus Web of Science® Altmetric
?
?
Full metadata record
DC FieldValueLanguage
dc.contributor.authorHardingham, J.-
dc.contributor.authorGrover, P.-
dc.contributor.authorWinter, M.-
dc.contributor.authorHewett, P.-
dc.contributor.authorPrice, T.-
dc.contributor.authorThierry, B.-
dc.date.issued2015-
dc.identifier.citationMolecular Medicine, 2015; 21(Suppl 1):S25-S31-
dc.identifier.issn1528-3658-
dc.identifier.issn1528-3658-
dc.identifier.urihttp://hdl.handle.net/2440/96490-
dc.description.abstractCirculating tumor cells (CTC) may be defined as tumor- or metastasis-derived cells that are present in the bloodstream. The CTC pool in colorectal cancer (CRC) patients may include not only epithelial tumor cells, but also tumor cells undergoing epithelial–mesenchymal transition (EMT) and tumor stem cells. A significant number of patients diagnosed with early stage CRC subsequently relapse with recurrent or metastatic disease despite undergoing “curative” resection of their primary tumor. This suggests that an occult metastatic disease process was already underway, with viable tumor cells being shed from the primary tumor site, at least some of which have proliferative and metastatic potential and the ability to survive in the bloodstream. Such tumor cells are considered to be responsible for disease relapse in these patients. Their detection in peripheral blood at the time of diagnosis or after resection of the primary tumor may identify those early-stage patients who are at risk of developing recurrent or metastatic disease and who would benefit from adjuvant therapy. CTC may also be a useful adjunct to radiological assessment of tumor response to therapy. Over the last 20 years many approaches have been developed for the isolation and characterization of CTC. However, none of these methods can be considered the gold standard for detection of the entire pool of CTC. Recently our group has developed novel unbiased inertial microfluidics to enrich for CTC, followed by identification of CTC by imaging flow cytometry. Here, we provide a review of progress on CTC detection and clinical significance over the last 20 years.-
dc.description.statementofresponsibilityJennifer E Hardingham, Phulwinder Grover, Marnie Winter, Peter J Hewett, Timothy J Price, and Benjamin Thierry-
dc.language.isoen-
dc.publisherFeinstein Institute for Medical Research-
dc.rights© The author-
dc.source.urihttp://dx.doi.org/10.2119/molmed.2015.00149-
dc.subjectEpithelial Cells-
dc.subjectHumans-
dc.subjectColorectal Neoplasms-
dc.subjectRecurrence-
dc.subjectGranulocyte Colony-Stimulating Factor-
dc.subjectReceptors, G-Protein-Coupled-
dc.subjectPrognosis-
dc.subjectCell Separation-
dc.subjectMicrofluidics-
dc.subjectGene Expression-
dc.subjectHistory, 20th Century-
dc.subjectHistory, 21st Century-
dc.subjectBasic Helix-Loop-Helix Transcription Factors-
dc.subjectNeoplastic Stem Cells-
dc.subjectNeoplastic Cells, Circulating-
dc.subjectEpithelial-Mesenchymal Transition-
dc.subjectBiomarkers-
dc.titleDetection and clinical significance of circulating tumor cells in colorectal cancer - 20 years of progress-
dc.typeJournal article-
dc.identifier.doi10.2119/molmed.2015.00149-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1045841-
pubs.publication-statusPublished-
dc.identifier.orcidHardingham, J. [0000-0001-8277-1199]-
dc.identifier.orcidPrice, T. [0000-0002-3922-2693]-
Appears in Collections:Aurora harvest 7
Medicine publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.