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dc.contributor.authorHamid, Faysal-Bin
dc.contributor.authorIslam, Farhad
dc.contributor.authorLu, Cu-Tai
dc.contributor.authorMatos, Marco
dc.contributor.authorCheng, Tracie
dc.contributor.authorGopalan, Vinod
dc.contributor.authorLam, Alfred King-yin
dc.date.accessioned2021-03-11T07:55:43Z
dc.date.available2021-03-11T07:55:43Z
dc.date.issued2020
dc.identifier.issn0008-5472
dc.identifier.doi10.1158/1538-7445.AM2020-5367
dc.identifier.urihttp://hdl.handle.net/10072/403080
dc.description.abstractThe number of circulating tumor cells (CTCs) hase been found as a promising predictive and diagnostic biomarker of colorectal cancer (CRC). The purpose of the study was to enumerate and characterize CTCs from the CRC patients and evaluate the correlation with the clinical stages.Peripheral blood from 57 CRC patients and 6 healthy donors were subjected to isolate CTC by a negative selection (EasySepTM) method. The CTCs were detected by the immunofluorescence staining with the tumor cell markers such as epithelial cell adhesion molecule (EPCAM) and cytokeratin (CK) antibodies and counted them. The extent of positive expressions of EPCAM and cytokeratin (CK) proteins were used to characterize the CTCs and the subpopulations were correlated with the tumor stages of the CRC patients. P<0.05 was considered as statistically significant.CTCs were detected in 72% (41/57) of the CRC patients. Comparing to the healthy donors (HD), the CTC count was higher (p=0.0062) in the CRC patients. In addition, CTC clusters were found in 32% (18/57) of patients with CRC while total CTCs were significantly higher than the cluster count (p=0.001). Among the CRC patients, CTCs were more abundant in the advanced stages compared to the early stages (p=0.0019). Moreover, we found the length of the individual CTCs were significantly larger than the CTCs in the cluster (p<0.0001) and significantly correlated (p=0.036) with the tumor stages. However, we identified the EPCAMPosCkPos subclones in 38 (93%) out of 41 CTC positive cases and a median of 8.0 (range: 0-60) CTCs were counted. In contrast, EPCAMPosCkNeg subpopulations were detected in 27 (66%) patients and the median CTC count was 2.0 (range: 0-18). Interestingly, EPCAMPosCkPos CTC subclones were significantly higher (p=0.011) than EPCAMPosCkNeg subclones, and the number of EPCAMPosCkPos CTCs was merely associated (p=0.0068) with the tumor stages. We conclude that the morphological and phenotypic features of the CTCs are closely relevant to the clinical stages, which could provide vital information to improve the patient stratification and treatment selection.
dc.languageEnglish
dc.publisherAmerican Association for Cancer Research
dc.relation.ispartofconferencenameAACR Annual Meeting
dc.relation.ispartofconferencetitleCancer Research
dc.relation.ispartofdatefrom2020-06-22
dc.relation.ispartofdateto2020-06-24
dc.relation.ispartoflocationOnline
dc.relation.ispartofissue16
dc.relation.ispartofvolume80
dc.subject.fieldofresearchOncology and Carcinogenesis
dc.subject.fieldofresearchcode1112
dc.subject.keywordsScience & Technology
dc.subject.keywordsLife Sciences & Biomedicine
dc.titleIdentification and clinical value of the circulating tumor cells (CTCs) in the colorectal cancer
dc.typeConference output
dc.type.descriptionE2 - Conferences (Non Refereed)
dcterms.bibliographicCitationHamid, F-B; Islam, F; Lu, C-T; Matos, M; Cheng, T; Gopalan, V; Lam, AK-Y, Identification and clinical value of the circulating tumor cells (CTCs) in the colorectal cancer, Cancer Research, 2020, 80 (16)
dc.date.updated2021-03-11T03:41:57Z
gro.hasfulltextNo Full Text
gro.griffith.authorLam, Alfred K.
gro.griffith.authorGopalan, Vinod
gro.griffith.authorCheng, Tracie T.
gro.griffith.authorHamid, Faysal-Bin


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