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The Role of High-Resolution Magic Angle Spinning 1H Nuclear Magnetic Resonance Spectroscopy for Predicting the Invasive Component in Patients with Ductal Carcinoma In Situ Diagnosed on Preoperative Biopsy

The purpose of this study was to evaluate the role of high-resolution magic angle spinning (HR-MAS) 1H nuclear magnetic resonance (NMR) spectroscopy in patients with ductal carcinoma in situ (DCIS) diagnosed on preoperative biopsy. We investigated whether the metabolic profiling of tissue samples us...

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Autores principales: Chae, Eun Young, Shin, Hee Jung, Kim, Suhkmann, Baek, Hyeon-Man, Yoon, Dahye, Kim, Siwon, Shim, Ye Eun, Kim, Hak Hee, Cha, Joo Hee, Choi, Woo Jung, Lee, Jeong Hyun, Shin, Ji Hoon, Lee, Hee Jin, Gong, Gyungyub
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999265/
https://www.ncbi.nlm.nih.gov/pubmed/27560937
http://dx.doi.org/10.1371/journal.pone.0161038
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author Chae, Eun Young
Shin, Hee Jung
Kim, Suhkmann
Baek, Hyeon-Man
Yoon, Dahye
Kim, Siwon
Shim, Ye Eun
Kim, Hak Hee
Cha, Joo Hee
Choi, Woo Jung
Lee, Jeong Hyun
Shin, Ji Hoon
Lee, Hee Jin
Gong, Gyungyub
author_facet Chae, Eun Young
Shin, Hee Jung
Kim, Suhkmann
Baek, Hyeon-Man
Yoon, Dahye
Kim, Siwon
Shim, Ye Eun
Kim, Hak Hee
Cha, Joo Hee
Choi, Woo Jung
Lee, Jeong Hyun
Shin, Ji Hoon
Lee, Hee Jin
Gong, Gyungyub
author_sort Chae, Eun Young
collection PubMed
description The purpose of this study was to evaluate the role of high-resolution magic angle spinning (HR-MAS) 1H nuclear magnetic resonance (NMR) spectroscopy in patients with ductal carcinoma in situ (DCIS) diagnosed on preoperative biopsy. We investigated whether the metabolic profiling of tissue samples using HR-MAS 1H NMR spectroscopy could be used to distinguish between DCIS lesions with or without an invasive component. Our institutional review board approved this combined retrospective and prospective study. Tissue samples were collected from 30 patients with pure DCIS and from 30 with DCIS accompanying invasive carcinoma. All patients were diagnosed with DCIS by preoperative core-needle biopsy and underwent surgical resection. The metabolic profiling of tissue samples was performed by HR-MAS 1H NMR spectroscopy. All observable metabolite signals were identified and quantified in all tissue samples. Metabolite intensity normalized by total spectral intensities was compared according to the tumor type using the Mann-Whitney test. Multivariate analysis was performed with orthogonal projections to latent structure-discriminant analysis (OPLS-DA). By univariate analysis, the metabolite concentrations of choline-containing compounds obtained with HR-MAS 1H NMR spectroscopy did not differ significantly between the pure DCIS and DCIS accompanying invasive carcinoma groups. However, the GPC/PC ratio was higher in the pure DCIS group than in the DCIS accompanying invasive carcinoma group (p = 0.004, Bonferroni-corrected p = 0.064), as well as the concentration of myo-inositol and succinate. By multivariate analysis, the OPLS-DA models built with HR-MAS MR metabolic profiles could clearly discriminate between pure DCIS and DCIS accompanying invasive carcinoma. Our preliminary results suggest that HR-MAS MR metabolomics on breast tissue may be able to distinguish between DCIS lesions with or without an invasive component.
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spelling pubmed-49992652016-09-12 The Role of High-Resolution Magic Angle Spinning 1H Nuclear Magnetic Resonance Spectroscopy for Predicting the Invasive Component in Patients with Ductal Carcinoma In Situ Diagnosed on Preoperative Biopsy Chae, Eun Young Shin, Hee Jung Kim, Suhkmann Baek, Hyeon-Man Yoon, Dahye Kim, Siwon Shim, Ye Eun Kim, Hak Hee Cha, Joo Hee Choi, Woo Jung Lee, Jeong Hyun Shin, Ji Hoon Lee, Hee Jin Gong, Gyungyub PLoS One Research Article The purpose of this study was to evaluate the role of high-resolution magic angle spinning (HR-MAS) 1H nuclear magnetic resonance (NMR) spectroscopy in patients with ductal carcinoma in situ (DCIS) diagnosed on preoperative biopsy. We investigated whether the metabolic profiling of tissue samples using HR-MAS 1H NMR spectroscopy could be used to distinguish between DCIS lesions with or without an invasive component. Our institutional review board approved this combined retrospective and prospective study. Tissue samples were collected from 30 patients with pure DCIS and from 30 with DCIS accompanying invasive carcinoma. All patients were diagnosed with DCIS by preoperative core-needle biopsy and underwent surgical resection. The metabolic profiling of tissue samples was performed by HR-MAS 1H NMR spectroscopy. All observable metabolite signals were identified and quantified in all tissue samples. Metabolite intensity normalized by total spectral intensities was compared according to the tumor type using the Mann-Whitney test. Multivariate analysis was performed with orthogonal projections to latent structure-discriminant analysis (OPLS-DA). By univariate analysis, the metabolite concentrations of choline-containing compounds obtained with HR-MAS 1H NMR spectroscopy did not differ significantly between the pure DCIS and DCIS accompanying invasive carcinoma groups. However, the GPC/PC ratio was higher in the pure DCIS group than in the DCIS accompanying invasive carcinoma group (p = 0.004, Bonferroni-corrected p = 0.064), as well as the concentration of myo-inositol and succinate. By multivariate analysis, the OPLS-DA models built with HR-MAS MR metabolic profiles could clearly discriminate between pure DCIS and DCIS accompanying invasive carcinoma. Our preliminary results suggest that HR-MAS MR metabolomics on breast tissue may be able to distinguish between DCIS lesions with or without an invasive component. Public Library of Science 2016-08-25 /pmc/articles/PMC4999265/ /pubmed/27560937 http://dx.doi.org/10.1371/journal.pone.0161038 Text en © 2016 Chae et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Chae, Eun Young
Shin, Hee Jung
Kim, Suhkmann
Baek, Hyeon-Man
Yoon, Dahye
Kim, Siwon
Shim, Ye Eun
Kim, Hak Hee
Cha, Joo Hee
Choi, Woo Jung
Lee, Jeong Hyun
Shin, Ji Hoon
Lee, Hee Jin
Gong, Gyungyub
The Role of High-Resolution Magic Angle Spinning 1H Nuclear Magnetic Resonance Spectroscopy for Predicting the Invasive Component in Patients with Ductal Carcinoma In Situ Diagnosed on Preoperative Biopsy
title The Role of High-Resolution Magic Angle Spinning 1H Nuclear Magnetic Resonance Spectroscopy for Predicting the Invasive Component in Patients with Ductal Carcinoma In Situ Diagnosed on Preoperative Biopsy
title_full The Role of High-Resolution Magic Angle Spinning 1H Nuclear Magnetic Resonance Spectroscopy for Predicting the Invasive Component in Patients with Ductal Carcinoma In Situ Diagnosed on Preoperative Biopsy
title_fullStr The Role of High-Resolution Magic Angle Spinning 1H Nuclear Magnetic Resonance Spectroscopy for Predicting the Invasive Component in Patients with Ductal Carcinoma In Situ Diagnosed on Preoperative Biopsy
title_full_unstemmed The Role of High-Resolution Magic Angle Spinning 1H Nuclear Magnetic Resonance Spectroscopy for Predicting the Invasive Component in Patients with Ductal Carcinoma In Situ Diagnosed on Preoperative Biopsy
title_short The Role of High-Resolution Magic Angle Spinning 1H Nuclear Magnetic Resonance Spectroscopy for Predicting the Invasive Component in Patients with Ductal Carcinoma In Situ Diagnosed on Preoperative Biopsy
title_sort role of high-resolution magic angle spinning 1h nuclear magnetic resonance spectroscopy for predicting the invasive component in patients with ductal carcinoma in situ diagnosed on preoperative biopsy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999265/
https://www.ncbi.nlm.nih.gov/pubmed/27560937
http://dx.doi.org/10.1371/journal.pone.0161038
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