Cargando…

A dried blood spot mass spectrometry metabolomic approach for rapid breast cancer detection

OBJECTIVE: Breast cancer (BC) is still a lethal threat to women worldwide. An accurate screening and diagnosis strategy performed in an easy-to-operate manner is highly warranted in clinical perspective. Besides the routinely focused protein markers, blood is full of small molecular metabolites with...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Qingjun, Sun, Tao, Cao, Yunfeng, Gao, Peng, Dong, Jun, Fang, Yanhua, Fang, Zhongze, Sun, Xiaoyu, Zhu, Zhitu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795570/
https://www.ncbi.nlm.nih.gov/pubmed/27042107
http://dx.doi.org/10.2147/OTT.S95862
_version_ 1782421623256645632
author Wang, Qingjun
Sun, Tao
Cao, Yunfeng
Gao, Peng
Dong, Jun
Fang, Yanhua
Fang, Zhongze
Sun, Xiaoyu
Zhu, Zhitu
author_facet Wang, Qingjun
Sun, Tao
Cao, Yunfeng
Gao, Peng
Dong, Jun
Fang, Yanhua
Fang, Zhongze
Sun, Xiaoyu
Zhu, Zhitu
author_sort Wang, Qingjun
collection PubMed
description OBJECTIVE: Breast cancer (BC) is still a lethal threat to women worldwide. An accurate screening and diagnosis strategy performed in an easy-to-operate manner is highly warranted in clinical perspective. Besides the routinely focused protein markers, blood is full of small molecular metabolites with diverse structures and properties. This study aimed to screen metabolite markers with BC diagnosis potentials. METHODS: A dried blood spot-based direct infusion mass spectrometry (MS) metabolomic analysis was conducted for BC and non-BC differentiation. The targeted analytes included 23 amino acids and 26 acylcarnitines. RESULTS: Multivariate analysis screened out 21 BC-related metabolites in the blood. Regression analysis generated a diagnosis model consisting of parameters Pip, Asn, Pro, C14:1/C16, Phe/Tyr, and Gly/Ala. Tested with another set of BC and non-BC samples, this model showed a sensitivity of 92.2% and a specificity of 84.4%. Compared to the routinely used protein markers, this model exhibited distinct advantage with its higher sensitivity. CONCLUSION: Blood metabolites screening is a more plausible approach for BC detection. Furthermore, this direct MS analysis could be finished within few minutes, which means that its throughput is higher than the currently used imaging techniques.
format Online
Article
Text
id pubmed-4795570
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-47955702016-04-01 A dried blood spot mass spectrometry metabolomic approach for rapid breast cancer detection Wang, Qingjun Sun, Tao Cao, Yunfeng Gao, Peng Dong, Jun Fang, Yanhua Fang, Zhongze Sun, Xiaoyu Zhu, Zhitu Onco Targets Ther Original Research OBJECTIVE: Breast cancer (BC) is still a lethal threat to women worldwide. An accurate screening and diagnosis strategy performed in an easy-to-operate manner is highly warranted in clinical perspective. Besides the routinely focused protein markers, blood is full of small molecular metabolites with diverse structures and properties. This study aimed to screen metabolite markers with BC diagnosis potentials. METHODS: A dried blood spot-based direct infusion mass spectrometry (MS) metabolomic analysis was conducted for BC and non-BC differentiation. The targeted analytes included 23 amino acids and 26 acylcarnitines. RESULTS: Multivariate analysis screened out 21 BC-related metabolites in the blood. Regression analysis generated a diagnosis model consisting of parameters Pip, Asn, Pro, C14:1/C16, Phe/Tyr, and Gly/Ala. Tested with another set of BC and non-BC samples, this model showed a sensitivity of 92.2% and a specificity of 84.4%. Compared to the routinely used protein markers, this model exhibited distinct advantage with its higher sensitivity. CONCLUSION: Blood metabolites screening is a more plausible approach for BC detection. Furthermore, this direct MS analysis could be finished within few minutes, which means that its throughput is higher than the currently used imaging techniques. Dove Medical Press 2016-03-11 /pmc/articles/PMC4795570/ /pubmed/27042107 http://dx.doi.org/10.2147/OTT.S95862 Text en © 2016 Wang 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
Wang, Qingjun
Sun, Tao
Cao, Yunfeng
Gao, Peng
Dong, Jun
Fang, Yanhua
Fang, Zhongze
Sun, Xiaoyu
Zhu, Zhitu
A dried blood spot mass spectrometry metabolomic approach for rapid breast cancer detection
title A dried blood spot mass spectrometry metabolomic approach for rapid breast cancer detection
title_full A dried blood spot mass spectrometry metabolomic approach for rapid breast cancer detection
title_fullStr A dried blood spot mass spectrometry metabolomic approach for rapid breast cancer detection
title_full_unstemmed A dried blood spot mass spectrometry metabolomic approach for rapid breast cancer detection
title_short A dried blood spot mass spectrometry metabolomic approach for rapid breast cancer detection
title_sort dried blood spot mass spectrometry metabolomic approach for rapid breast cancer detection
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795570/
https://www.ncbi.nlm.nih.gov/pubmed/27042107
http://dx.doi.org/10.2147/OTT.S95862
work_keys_str_mv AT wangqingjun adriedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection
AT suntao adriedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection
AT caoyunfeng adriedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection
AT gaopeng adriedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection
AT dongjun adriedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection
AT fangyanhua adriedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection
AT fangzhongze adriedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection
AT sunxiaoyu adriedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection
AT zhuzhitu adriedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection
AT wangqingjun driedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection
AT suntao driedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection
AT caoyunfeng driedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection
AT gaopeng driedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection
AT dongjun driedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection
AT fangyanhua driedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection
AT fangzhongze driedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection
AT sunxiaoyu driedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection
AT zhuzhitu driedbloodspotmassspectrometrymetabolomicapproachforrapidbreastcancerdetection