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Optical coding of fusion genes using multicolor quantum dots for prostate cancer diagnosis
Recent 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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5476632/ https://www.ncbi.nlm.nih.gov/pubmed/28652740 http://dx.doi.org/10.2147/IJN.S138081 |
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author | Lee, Hyojin Kim, Chloe Lee, Dongjin Park, Jea Ho Searson, Peter C Lee, Kwan Hyi |
author_facet | Lee, Hyojin Kim, Chloe Lee, Dongjin Park, Jea Ho Searson, Peter C Lee, Kwan Hyi |
author_sort | Lee, Hyojin |
collection | PubMed |
description | Recent 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. |
format | Online Article Text |
id | pubmed-5476632 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54766322017-06-26 Optical coding of fusion genes using multicolor quantum dots for prostate cancer diagnosis Lee, Hyojin Kim, Chloe Lee, Dongjin Park, Jea Ho Searson, Peter C Lee, Kwan Hyi Int J Nanomedicine Original Research Recent 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. Dove Medical Press 2017-06-12 /pmc/articles/PMC5476632/ /pubmed/28652740 http://dx.doi.org/10.2147/IJN.S138081 Text en © 2017 Lee et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Lee, Hyojin Kim, Chloe Lee, Dongjin Park, Jea Ho Searson, Peter C Lee, Kwan Hyi Optical coding of fusion genes using multicolor quantum dots for prostate cancer diagnosis |
title | Optical coding of fusion genes using multicolor quantum dots for prostate cancer diagnosis |
title_full | Optical coding of fusion genes using multicolor quantum dots for prostate cancer diagnosis |
title_fullStr | Optical coding of fusion genes using multicolor quantum dots for prostate cancer diagnosis |
title_full_unstemmed | Optical coding of fusion genes using multicolor quantum dots for prostate cancer diagnosis |
title_short | Optical coding of fusion genes using multicolor quantum dots for prostate cancer diagnosis |
title_sort | optical coding of fusion genes using multicolor quantum dots for prostate cancer diagnosis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5476632/ https://www.ncbi.nlm.nih.gov/pubmed/28652740 http://dx.doi.org/10.2147/IJN.S138081 |
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