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Extracellular vesicle biomarkers for pancreatic cancer diagnosis: a systematic review and meta-analysis

BACKGROUND: Extracellular vesicle (EV) biomarkers have promising diagnosis and screening capacity for several cancers, but the diagnostic value for pancreatic cancer (PC) is controversial. The aim of our study was to review the diagnostic performance of EV biomarkers for PC. METHODS: We performed a...

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Autores principales: Jia, Erna, Ren, Na, Shi, Xianquan, Zhang, Rongkui, Yu, Haixin, Yu, Fan, Qin, Shaoyou, Xue, Jinru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9125932/
https://www.ncbi.nlm.nih.gov/pubmed/35606727
http://dx.doi.org/10.1186/s12885-022-09463-x
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author Jia, Erna
Ren, Na
Shi, Xianquan
Zhang, Rongkui
Yu, Haixin
Yu, Fan
Qin, Shaoyou
Xue, Jinru
author_facet Jia, Erna
Ren, Na
Shi, Xianquan
Zhang, Rongkui
Yu, Haixin
Yu, Fan
Qin, Shaoyou
Xue, Jinru
author_sort Jia, Erna
collection PubMed
description BACKGROUND: Extracellular vesicle (EV) biomarkers have promising diagnosis and screening capacity for several cancers, but the diagnostic value for pancreatic cancer (PC) is controversial. The aim of our study was to review the diagnostic performance of EV biomarkers for PC. METHODS: We performed a systematic review of PubMed, Medline, and Web Of Science databases from inception to 18 Feb 2022. We identified studies reporting the diagnostic performance of EV biomarkers for PC and summarized the information of sensitivity, specificity, area under the curve (AUC), or receiver operator characteristic (ROC) curve) in according to a pre-designed data collection form. Pooled sensitivity and specificity was calculated using a random-effect model. RESULTS: We identified 39 studies, including 2037 PC patients and 1632 noncancerous, seven of which were conducted independent validation tests. Seventeen studies emphasized on EV RNAs, sixteen on EV proteins, and sixteen on biomarker panels. MiR-10b, miR-21, and GPC1 were the most frequently reported RNA and protein for PC diagnosis. For individual RNAs and proteins, the pooled sensitivity and specificity were 79% (95% CI: 77–81%) and 87% (95% CI: 85–89%), 72% (95% CI: 69–74%) and 77% (95% CI: 74–80%), respectively. the pooled sensitivity and specificity of EV RNA combined with protein panels were 84% (95% CI: 81–86%) and 89% (95% CI: 86–91%), respectively. Surprisingly, for early stage (stage I and II) PC EV biomarkers showed excellent diagnostic performance with the sensitivity of 90% (95% CI: 87–93%) and the specificity of 94% (95% CI: 92–95%). Both in sensitivity and subgroup analyses, we did not observe notable difference in pooled sensitivity and specificity. Studies might be limited by the isolation and detection techniques of EVs to a certain extent. CONCLUSIONS: EV biomarkers showed appealing diagnostic preference for PC, especially for early stage PC. Solving the deficiency of technologies of isolation and detection EVs has important implications for application these novel noninvasive biomarkers in clinical practice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-09463-x.
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spelling pubmed-91259322022-05-24 Extracellular vesicle biomarkers for pancreatic cancer diagnosis: a systematic review and meta-analysis Jia, Erna Ren, Na Shi, Xianquan Zhang, Rongkui Yu, Haixin Yu, Fan Qin, Shaoyou Xue, Jinru BMC Cancer Research BACKGROUND: Extracellular vesicle (EV) biomarkers have promising diagnosis and screening capacity for several cancers, but the diagnostic value for pancreatic cancer (PC) is controversial. The aim of our study was to review the diagnostic performance of EV biomarkers for PC. METHODS: We performed a systematic review of PubMed, Medline, and Web Of Science databases from inception to 18 Feb 2022. We identified studies reporting the diagnostic performance of EV biomarkers for PC and summarized the information of sensitivity, specificity, area under the curve (AUC), or receiver operator characteristic (ROC) curve) in according to a pre-designed data collection form. Pooled sensitivity and specificity was calculated using a random-effect model. RESULTS: We identified 39 studies, including 2037 PC patients and 1632 noncancerous, seven of which were conducted independent validation tests. Seventeen studies emphasized on EV RNAs, sixteen on EV proteins, and sixteen on biomarker panels. MiR-10b, miR-21, and GPC1 were the most frequently reported RNA and protein for PC diagnosis. For individual RNAs and proteins, the pooled sensitivity and specificity were 79% (95% CI: 77–81%) and 87% (95% CI: 85–89%), 72% (95% CI: 69–74%) and 77% (95% CI: 74–80%), respectively. the pooled sensitivity and specificity of EV RNA combined with protein panels were 84% (95% CI: 81–86%) and 89% (95% CI: 86–91%), respectively. Surprisingly, for early stage (stage I and II) PC EV biomarkers showed excellent diagnostic performance with the sensitivity of 90% (95% CI: 87–93%) and the specificity of 94% (95% CI: 92–95%). Both in sensitivity and subgroup analyses, we did not observe notable difference in pooled sensitivity and specificity. Studies might be limited by the isolation and detection techniques of EVs to a certain extent. CONCLUSIONS: EV biomarkers showed appealing diagnostic preference for PC, especially for early stage PC. Solving the deficiency of technologies of isolation and detection EVs has important implications for application these novel noninvasive biomarkers in clinical practice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-09463-x. BioMed Central 2022-05-23 /pmc/articles/PMC9125932/ /pubmed/35606727 http://dx.doi.org/10.1186/s12885-022-09463-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visithttp://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Jia, Erna
Ren, Na
Shi, Xianquan
Zhang, Rongkui
Yu, Haixin
Yu, Fan
Qin, Shaoyou
Xue, Jinru
Extracellular vesicle biomarkers for pancreatic cancer diagnosis: a systematic review and meta-analysis
title Extracellular vesicle biomarkers for pancreatic cancer diagnosis: a systematic review and meta-analysis
title_full Extracellular vesicle biomarkers for pancreatic cancer diagnosis: a systematic review and meta-analysis
title_fullStr Extracellular vesicle biomarkers for pancreatic cancer diagnosis: a systematic review and meta-analysis
title_full_unstemmed Extracellular vesicle biomarkers for pancreatic cancer diagnosis: a systematic review and meta-analysis
title_short Extracellular vesicle biomarkers for pancreatic cancer diagnosis: a systematic review and meta-analysis
title_sort extracellular vesicle biomarkers for pancreatic cancer diagnosis: a systematic review and meta-analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9125932/
https://www.ncbi.nlm.nih.gov/pubmed/35606727
http://dx.doi.org/10.1186/s12885-022-09463-x
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