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dc.contributor.authorLee, Hyojin-
dc.contributor.authorKim, Chloe-
dc.contributor.authorLee, Dongjin-
dc.contributor.authorPark, Jea Ho-
dc.contributor.authorSearson, Peter C.-
dc.contributor.authorLee, Kwan Hyi-
dc.date.accessioned2024-01-20T01:31:18Z-
dc.date.available2024-01-20T01:31:18Z-
dc.date.created2021-09-04-
dc.date.issued2017-06-
dc.identifier.issn1176-9114-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/122695-
dc.description.abstractRecent studies have found that prostate cancer expresses abnormal genetic markers including multiple types of TMPRSS2-ERG fusion genes. The expression level of different TMPRSS2-ERG fusion genes is correlated to pathologic variables of aggressive prostate cancer and disease progression. State-of-the-art methods for detection of TMPRSS2-ERG fusion genes include reverse transcription polymerase chain reaction (RT-PCR) with a detection limit of 1 fmol at urinary condition. RT-PCR is time consuming, costly, and inapplicable for multiplexing. Ability to identify multiple fusion genes in a single sample has become important for diagnostic and clinical purposes. There is a need for a sensitive diagnostic test to detect multiple TMPRSS2-ERG fusion genes for an early diagnosis and prognosis of prostate cancer. Here, we propose to develop an assay for prostate cancer diagnosis using oligonucleotide-functionalized quantum dot and magnetic microparticle for optical detection of rearranged TMPRSS2-ERG fusion genes at a low concentration in urine. We found that our assay was able to identify three different types of fusion gene with a wide detection range and detection limit of 1 fmol (almost the same level of the RT-PCR result reported). Here, we show detection of multiple TMPRSS2-ERG fusion genes using color-coded oligonucleotides in cell lysate and urine.-
dc.languageEnglish-
dc.publisherDOVE MEDICAL PRESS LTD-
dc.subjectMOLECULAR CHARACTERIZATION-
dc.subjectCHEMISTRY-
dc.titleOptical coding of fusion genes using multicolor quantum dots for prostate cancer diagnosis-
dc.typeArticle-
dc.identifier.doi10.2147/IJN.S138081-
dc.description.journalClass1-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF NANOMEDICINE, v.12, pp.4397 - 4407-
dc.citation.titleINTERNATIONAL JOURNAL OF NANOMEDICINE-
dc.citation.volume12-
dc.citation.startPage4397-
dc.citation.endPage4407-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000403229800003-
dc.identifier.scopusid2-s2.0-85020934654-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeArticle-
dc.subject.keywordPlusMOLECULAR CHARACTERIZATION-
dc.subject.keywordPlusCHEMISTRY-
dc.subject.keywordAuthorfusion genes-
dc.subject.keywordAuthorprostate cancer-
dc.subject.keywordAuthorquantum dots-
dc.subject.keywordAuthormultiplexed assay-
dc.subject.keywordAuthoroptical detection-
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KIST Article > 2017
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