Publication: Magnetic Nanoparticles PCR Enzyme-Linked Gene Assay for Quantitative Detection of BCR/ABL Fusion Gene in Chronic Myelogenous Leukemia
dc.contributor.author | Yanaphat Manthawornsiri | en_US |
dc.contributor.author | Duangporn Polpanich | en_US |
dc.contributor.author | Vichanan Yamkamon | en_US |
dc.contributor.author | Raweewan Thiramanas | en_US |
dc.contributor.author | Suradej Hongeng | en_US |
dc.contributor.author | Budsaba Rerkamnuaychoke | en_US |
dc.contributor.author | Saengsuree Jootar | en_US |
dc.contributor.author | Pramuan Tangboriboonrat | en_US |
dc.contributor.author | Kulachart Jangpatarapongsa | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.contributor.other | Thailand National Nanotechnology Center | en_US |
dc.date.accessioned | 2018-12-11T02:10:19Z | |
dc.date.accessioned | 2019-03-14T08:03:57Z | |
dc.date.available | 2018-12-11T02:10:19Z | |
dc.date.available | 2019-03-14T08:03:57Z | |
dc.date.issued | 2016-09-01 | en_US |
dc.description.abstract | © 2015 Wiley Periodicals, Inc. Background: Magnetic nanoparticles (MNPs) have been widely used in medical diagnostic research. In this work, two technologies, MNPs and polymerase chain reaction (PCR), were combined to increase detection sensitivity and specificity. A novel technique based on the MNPs-PCR enzyme-linked gene assay (MELGA) was developed for detection of the BCR/ABL abnormal gene in chronic myelogenous leukemia (CML) patients. Methods: An MNPs-labeled BCR forward primer and a biotin-labeled ABL reverse primer were used to specifically amplify the target gene. After magnetic separation, the PCR product bound to MNPs labeled with streptavidin-conjugated horseradish peroxidase was incubated with the peroxidase substrate and hydrogen peroxide to generate the colorimetric signal. Results: When compared with real-time quantitative-PCR (RQ-PCR), the MELGA technique exhibited an increased sensitivity of <1 fg with high specificity for the BCR/ABL fusion gene in CML patients. In addition, MELGA colorimetric results correlated well with the number of copies obtained from RQ-PCR. Conclusion: This simple and cost-effective technique is suitable for monitoring CML patients during targeted therapy (tyrosine kinase inhibitors) especially in rural hospitals. | en_US |
dc.identifier.citation | Journal of Clinical Laboratory Analysis. Vol.30, No.5 (2016), 534-542 | en_US |
dc.identifier.doi | 10.1002/jcla.21899 | en_US |
dc.identifier.issn | 10982825 | en_US |
dc.identifier.issn | 08878013 | en_US |
dc.identifier.other | 2-s2.0-84989244083 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/42906 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84989244083&origin=inward | en_US |
dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Health Professions | en_US |
dc.subject | Medicine | en_US |
dc.title | Magnetic Nanoparticles PCR Enzyme-Linked Gene Assay for Quantitative Detection of BCR/ABL Fusion Gene in Chronic Myelogenous Leukemia | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84989244083&origin=inward | en_US |