File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Isolation of circulating plasma cells from blood of patients diagnosed with clonal plasma cell disorders using cell selection microfluidics

Author(s)
Kamande, Joyce W.Lindell, Maria A. M.Witek, Malgorzata A.Voorhees, Peter M.Soper, Steven A.
Issued Date
2018-02
DOI
10.1039/c7ib00183e
URI
https://scholarworks.unist.ac.kr/handle/201301/23833
Fulltext
http://pubs.rsc.org/en/Content/ArticleLanding/2018/IB/C7IB00183E#!divAbstract
Citation
INTEGRATIVE BIOLOGY, v.10, no.2, pp.82 - 91
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.
Publisher
ROYAL SOC CHEMISTRY
ISSN
1757-9694
Keyword
SMOLDERING MULTIPLE-MYELOMAMINIMAL RESIDUAL DISEASEUNDETERMINED SIGNIFICANCE MGUSMONOCLONAL GAMMOPATHYTUMOR-CELLSPERIPHERAL-BLOODFLOW-CYTOMETRYK-RASACTIVATING MUTATIONSHIGH-RISK

qrcode

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