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dc.citation.endPage 91 -
dc.citation.number 2 -
dc.citation.startPage 82 -
dc.citation.title INTEGRATIVE BIOLOGY -
dc.citation.volume 10 -
dc.contributor.author Kamande, Joyce W. -
dc.contributor.author Lindell, Maria A. M. -
dc.contributor.author Witek, Malgorzata A. -
dc.contributor.author Voorhees, Peter M. -
dc.contributor.author Soper, Steven A. -
dc.date.accessioned 2023-12-21T21:09:52Z -
dc.date.available 2023-12-21T21:09:52Z -
dc.date.created 2018-03-12 -
dc.date.issued 2018-02 -
dc.description.abstract Blood samples from patients with plasma cell disorders were analysed for the presence of circulating plasma cells (CPCs) using a microfluidic device modified with monoclonal anti-CD138 antibodies. CPCs were immuno-phenotyped using a CD38/CD56/CD45 panel and identified in 78% of patients with monoclonal gammopathy of undetermined significance (MGUS), all patients with smouldering and symptomatic multiple myeloma (MM), and none in the controls. The burden of CPCs was higher in patients with symptomatic MM compared with MGUS and smouldering MM (p < 0.05). FISH analysis revealed the presence of chromosome 13 deletions in CPCs that correlated with bone marrow results. Point mutations in KRAS were identified, including different mutations from sub-clones derived from the same patient. The microfluidic assay represents a highly sensitive method for enumerating CPCs and allows for the cytogenetic and molecular characterization of CPCs. -
dc.identifier.bibliographicCitation INTEGRATIVE BIOLOGY, v.10, no.2, pp.82 - 91 -
dc.identifier.doi 10.1039/c7ib00183e -
dc.identifier.issn 1757-9694 -
dc.identifier.scopusid 2-s2.0-85042470787 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/23833 -
dc.identifier.url http://pubs.rsc.org/en/Content/ArticleLanding/2018/IB/C7IB00183E#!divAbstract -
dc.identifier.wosid 000425443400001 -
dc.language 영어 -
dc.publisher ROYAL SOC CHEMISTRY -
dc.title Isolation of circulating plasma cells from blood of patients diagnosed with clonal plasma cell disorders using cell selection microfluidics -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Cell Biology -
dc.relation.journalResearchArea Cell Biology -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus SMOLDERING MULTIPLE-MYELOMA -
dc.subject.keywordPlus MINIMAL RESIDUAL DISEASE -
dc.subject.keywordPlus UNDETERMINED SIGNIFICANCE MGUS -
dc.subject.keywordPlus MONOCLONAL GAMMOPATHY -
dc.subject.keywordPlus TUMOR-CELLS -
dc.subject.keywordPlus PERIPHERAL-BLOOD -
dc.subject.keywordPlus FLOW-CYTOMETRY -
dc.subject.keywordPlus K-RAS -
dc.subject.keywordPlus ACTIVATING MUTATIONS -
dc.subject.keywordPlus HIGH-RISK -

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