Serum-Based Quantification of MYCN Gene Amplification in Young Patients with Neuroblastoma: Potential Utility as a Surrogate Biomarker for Neuroblastoma.

We previously developed a method for determining MYCN gene amplification status using cell-free DNA fragments released from cancer cells into the blood of patients with neuroblastoma (NB). Here, we analyzed the relationship between MYCN amplification (MNA) status and neuroblastoma prognosis. We scre...

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Main Authors: Shigeki Yagyu, Tomoko Iehara, Shiro Tanaka, Takahiro Gotoh, Akiko Misawa-Furihata, Tohru Sugimoto, Wendy B London, Michael D Hogarty, Satoshi Teramukai, Akira Nakagawara, Eiso Hiyama, John M Maris, Hajime Hosoi
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4981470?pdf=render
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author Shigeki Yagyu
Tomoko Iehara
Shiro Tanaka
Takahiro Gotoh
Akiko Misawa-Furihata
Tohru Sugimoto
Wendy B London
Michael D Hogarty
Satoshi Teramukai
Akira Nakagawara
Eiso Hiyama
John M Maris
Hajime Hosoi
author_facet Shigeki Yagyu
Tomoko Iehara
Shiro Tanaka
Takahiro Gotoh
Akiko Misawa-Furihata
Tohru Sugimoto
Wendy B London
Michael D Hogarty
Satoshi Teramukai
Akira Nakagawara
Eiso Hiyama
John M Maris
Hajime Hosoi
author_sort Shigeki Yagyu
collection DOAJ
description We previously developed a method for determining MYCN gene amplification status using cell-free DNA fragments released from cancer cells into the blood of patients with neuroblastoma (NB). Here, we analyzed the relationship between MYCN amplification (MNA) status and neuroblastoma prognosis. We screened serum samples from 151 patients with NB for MNA, using real-time quantitative PCR, and compared the results with MYCN status determined using paired tumor samples. We additionally investigated whether MNA status correlates with patient survival. When a cut-off value of 5 was used, serum-based MNA analysis was found to show good sensitivity (86%) and very high specificity (95%). The sensitivities for stage 1 and 2 might be acceptable, even though it is not as good as for stage 3 and 4 (67% for stage 1 and 2, 92% for stage 3, and 87% for stage 4). MNA status correlated with overall survival in our cohort of 82 patients, with survival data available (p < 0.01). The hazard ratio of MNA status was 4.98 in patients diagnosed at less than 18 months of age (95% confidence interval, 1.00-24.78), and 1.41 (95% confidence interval, 0.63-3.14) for those diagnosed at 18 months of age or older. Serum-based MNA analysis is rapid and non-invasive compared with tumor-based MNA analysis, and has potential to predict tumor MNA status. There is still a room to improve the sensitivity of the test for tumors of stages 1 and 2, nonetheless this assay might help to determine therapeutic strategies prior to tumor biopsy, especially for patients with a life-threatening condition, as well as for patients of less than 18 months of age whose risk-grouping and treatment allocation depends on their MNA status.
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spelling doaj.art-623bd94eed5241259ab578803041b0632022-12-21T19:01:31ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01118e016103910.1371/journal.pone.0161039Serum-Based Quantification of MYCN Gene Amplification in Young Patients with Neuroblastoma: Potential Utility as a Surrogate Biomarker for Neuroblastoma.Shigeki YagyuTomoko IeharaShiro TanakaTakahiro GotohAkiko Misawa-FurihataTohru SugimotoWendy B LondonMichael D HogartySatoshi TeramukaiAkira NakagawaraEiso HiyamaJohn M MarisHajime HosoiWe previously developed a method for determining MYCN gene amplification status using cell-free DNA fragments released from cancer cells into the blood of patients with neuroblastoma (NB). Here, we analyzed the relationship between MYCN amplification (MNA) status and neuroblastoma prognosis. We screened serum samples from 151 patients with NB for MNA, using real-time quantitative PCR, and compared the results with MYCN status determined using paired tumor samples. We additionally investigated whether MNA status correlates with patient survival. When a cut-off value of 5 was used, serum-based MNA analysis was found to show good sensitivity (86%) and very high specificity (95%). The sensitivities for stage 1 and 2 might be acceptable, even though it is not as good as for stage 3 and 4 (67% for stage 1 and 2, 92% for stage 3, and 87% for stage 4). MNA status correlated with overall survival in our cohort of 82 patients, with survival data available (p < 0.01). The hazard ratio of MNA status was 4.98 in patients diagnosed at less than 18 months of age (95% confidence interval, 1.00-24.78), and 1.41 (95% confidence interval, 0.63-3.14) for those diagnosed at 18 months of age or older. Serum-based MNA analysis is rapid and non-invasive compared with tumor-based MNA analysis, and has potential to predict tumor MNA status. There is still a room to improve the sensitivity of the test for tumors of stages 1 and 2, nonetheless this assay might help to determine therapeutic strategies prior to tumor biopsy, especially for patients with a life-threatening condition, as well as for patients of less than 18 months of age whose risk-grouping and treatment allocation depends on their MNA status.http://europepmc.org/articles/PMC4981470?pdf=render
spellingShingle Shigeki Yagyu
Tomoko Iehara
Shiro Tanaka
Takahiro Gotoh
Akiko Misawa-Furihata
Tohru Sugimoto
Wendy B London
Michael D Hogarty
Satoshi Teramukai
Akira Nakagawara
Eiso Hiyama
John M Maris
Hajime Hosoi
Serum-Based Quantification of MYCN Gene Amplification in Young Patients with Neuroblastoma: Potential Utility as a Surrogate Biomarker for Neuroblastoma.
PLoS ONE
title Serum-Based Quantification of MYCN Gene Amplification in Young Patients with Neuroblastoma: Potential Utility as a Surrogate Biomarker for Neuroblastoma.
title_full Serum-Based Quantification of MYCN Gene Amplification in Young Patients with Neuroblastoma: Potential Utility as a Surrogate Biomarker for Neuroblastoma.
title_fullStr Serum-Based Quantification of MYCN Gene Amplification in Young Patients with Neuroblastoma: Potential Utility as a Surrogate Biomarker for Neuroblastoma.
title_full_unstemmed Serum-Based Quantification of MYCN Gene Amplification in Young Patients with Neuroblastoma: Potential Utility as a Surrogate Biomarker for Neuroblastoma.
title_short Serum-Based Quantification of MYCN Gene Amplification in Young Patients with Neuroblastoma: Potential Utility as a Surrogate Biomarker for Neuroblastoma.
title_sort serum based quantification of mycn gene amplification in young patients with neuroblastoma potential utility as a surrogate biomarker for neuroblastoma
url http://europepmc.org/articles/PMC4981470?pdf=render
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