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Detection of circulating tumor cell-specific markers in breast cancer patients using the quantitative RT-PCR assay

DC Field Value Language
dc.contributor.author김승일-
dc.contributor.author손주혁-
dc.contributor.author한현주-
dc.date.accessioned2018-01-23T05:48:52Z-
dc.date.available2018-01-23T05:48:52Z-
dc.date.issued2015-
dc.identifier.issn1341-9625-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/155660-
dc.description.abstractBACKGROUND: Breast cancer is a highly prevalent disease among women worldwide. While the expression of certain proteins within breast cancer tumors is used to determine the prognosis and select therapies, additional markers need to be identified. Circulating tumor cells (CTCs) are constituent cells that have detached from a primary tumor to circulate in the bloodstream. CTCs are considered the main source of breast cancer metastases; therefore, detection of CTCs could be a promising diagnostic method for metastatic breast cancer. METHODS: In this study, the CircleGen CTC RT-qDx assay was used to analyze the mRNA expression levels of six CTC-specific markers including EpCAM, CK19, HER2, Ki67, hTERT, and vimentin with a total of 692 peripheral whole blood samples from 221 breast cancer patients and 376 healthy individuals. RESULTS: This assay showed high specificity with multiple markers; none of the healthy controls were detected positive, whereas 21.7 and 14 % of breast cancer patients were positive for EpCAM and CK19, respectively. Of the 221 breast cancer patients, 84 (38 %), 46 (20.8 %), 83 (37.6 %), and 39 (17.6 %) were positively for HER2, Ki67, hTERT, and vimentin mRNA, respectively. Of the 84 patients who were HER2 positive, nine (4 %) were also positive for EpCAM, CK19, Ki67, hTERT, and vimentin. Of the 139 breast cancer patients who were HER2 negative, 65 (29.1 %) were negative for EpCAM, CK19, Ki67, hTERT, and vimentin. Furthermore, the EpCAM-positive population decreased from 21.5 to 8.3 % after completion of anti-tumor treatment (TP4). Similarly, the CK19, HER2, hTERT, and vimentin positives also decreased from 13.9 to 9.5 %, from 37.7 to 21.4 %, from 37.2 to 33.3 %, and from 17.5 to 14.3 %, respectively, after completion of anti-tumor treatment. In contrast, the Ki67 positives increased from 20.6 to 41.7 % after completion of anti-tumor treatment. CONCLUSIONS: mRNA overexpression of six CTC-specific markers was detected by the CircleGen CTC RT-qDx assay with high specificity, and the obtained mRNA expression levels of CTC-specific markers might provide useful criteria to select appropriate anti-tumor treatment for breast cancer patients.-
dc.description.statementOfResponsibilityrestriction-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF CLINICAL ONCOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHBiomarkers, Tumor/blood-
dc.subject.MESHBiomarkers, Tumor/genetics-
dc.subject.MESHBiomarkers, Tumor/metabolism*-
dc.subject.MESHBreast Neoplasms/blood-
dc.subject.MESHBreast Neoplasms/genetics-
dc.subject.MESHBreast Neoplasms/metabolism*-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplastic Cells, Circulating/metabolism*-
dc.subject.MESHReverse Transcriptase Polymerase Chain Reaction*-
dc.subject.MESHYoung Adult-
dc.titleDetection of circulating tumor cell-specific markers in breast cancer patients using the quantitative RT-PCR assay-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Surgery-
dc.contributor.googleauthorHye-young Wang-
dc.contributor.googleauthorSungwoo Ahn-
dc.contributor.googleauthorSunghyun Kim-
dc.contributor.googleauthorSunyoung Park-
dc.contributor.googleauthorDongju Jung-
dc.contributor.googleauthorSangjung Park-
dc.contributor.googleauthorHyunju Han-
dc.contributor.googleauthorJooHyuk Sohn-
dc.contributor.googleauthorSeungIl Kim-
dc.contributor.googleauthorHyeyoung Lee-
dc.identifier.doi10.1007/s10147-015-0798-3-
dc.contributor.localIdA00658-
dc.contributor.localIdA01995-
dc.contributor.localIdA04332-
dc.relation.journalcodeJ01097-
dc.identifier.eissn1437-7772-
dc.identifier.pmid25708591-
dc.identifier.urlhttp://link.springer.com/article/10.1007%2Fs10147-015-0798-3-
dc.subject.keywordAnti-tumor treatment-
dc.subject.keywordBreast cancer-
dc.subject.keywordCirculating tumor cells (CTCs)-
dc.subject.keywordMolecular diagnosis-
dc.subject.keywordRT-qPCR-
dc.contributor.alternativeNameKim, Seung Il-
dc.contributor.alternativeNameSohn, Joo Hyuk-
dc.contributor.alternativeNameHan, Hyun Ju-
dc.contributor.affiliatedAuthorKim, Seung Il-
dc.contributor.affiliatedAuthorSohn, Joo Hyuk-
dc.contributor.affiliatedAuthorHan, Hyun Ju-
dc.citation.volume20-
dc.citation.number5-
dc.citation.startPage878-
dc.citation.endPage890-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF CLINICAL ONCOLOGY, Vol.20(5) : 878-890, 2015-
dc.identifier.rimsid48124-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers

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