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Evaluation of the Diagnostic Potential of a Plasma Exosomal miRNAs Panel for Gastric Cancer

PURPOSE: Gastric cancer (GC) is often difficult to diagnose early in the disease and remains one of the most frequently occurring malignancies. This investigation looks at the diagnostic potential of a specific plasma exosomal miRNAs panel for GC. METHODS: This study analyzed 216 individual peripher...

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Autores principales: Yang, Jiajia, Li, Xuan, Wei, Shuchun, Peng, Lei, Sang, Huaiming, Jin, Duochen, Chen, Meihong, Dang, Yini, Zhang, Guoxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8371241/
https://www.ncbi.nlm.nih.gov/pubmed/34422636
http://dx.doi.org/10.3389/fonc.2021.683465
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author Yang, Jiajia
Li, Xuan
Wei, Shuchun
Peng, Lei
Sang, Huaiming
Jin, Duochen
Chen, Meihong
Dang, Yini
Zhang, Guoxin
author_facet Yang, Jiajia
Li, Xuan
Wei, Shuchun
Peng, Lei
Sang, Huaiming
Jin, Duochen
Chen, Meihong
Dang, Yini
Zhang, Guoxin
author_sort Yang, Jiajia
collection PubMed
description PURPOSE: Gastric cancer (GC) is often difficult to diagnose early in the disease and remains one of the most frequently occurring malignancies. This investigation looks at the diagnostic potential of a specific plasma exosomal miRNAs panel for GC. METHODS: This study analyzed 216 individual peripheral blood samples. 2 GEO datasets were analyzed and two miRNAs were selected - plasma exosomal miR-195-5p and miR-211-5p. Quantitative reverse-transcriptase PCR (qRT–PCR) was used to assess relative expressions and receiver operating characteristic (ROC) curve analysis was used to determine the diagnostic efficiency of miR-195-5p and miR-211-5p panel. The Kaplan-Meier method was used to assess the prognostic value of plasma exosomal miR-195-5p and miR-211-5p. RESULTS: GC patients possessed notably raised plasma levels of exosomal miR-195-5p and miR-211-5p. The area under ROC curves (AUCs) of miR-195-5p, miR-211-5p were 0.745, 0.798 in the screening phase and 0.762, 0.798 in the training stage respectively. GC was able to be diagnosed more accurately when both miRNAs were interpreted together (AUC=0.820 in the validation stage). Poorer prognosis was observed in GC patients who had plasma exosomal miR-195-5p and miR-211-5p of higher levels. In vitro experiments also confirmed that miR-195-5p and miR-211-5p is able to be transmitted between cells, and works to enhance tumor invasion, migration and proliferation while inhibiting cell apoptosis. CONCLUSION: Plasma exosomal miR-195-5p and miR-211-5p may become potential biomarkers for GC diagnosis, and may be useful in predicting tumor phenotype.
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spelling pubmed-83712412021-08-19 Evaluation of the Diagnostic Potential of a Plasma Exosomal miRNAs Panel for Gastric Cancer Yang, Jiajia Li, Xuan Wei, Shuchun Peng, Lei Sang, Huaiming Jin, Duochen Chen, Meihong Dang, Yini Zhang, Guoxin Front Oncol Oncology PURPOSE: Gastric cancer (GC) is often difficult to diagnose early in the disease and remains one of the most frequently occurring malignancies. This investigation looks at the diagnostic potential of a specific plasma exosomal miRNAs panel for GC. METHODS: This study analyzed 216 individual peripheral blood samples. 2 GEO datasets were analyzed and two miRNAs were selected - plasma exosomal miR-195-5p and miR-211-5p. Quantitative reverse-transcriptase PCR (qRT–PCR) was used to assess relative expressions and receiver operating characteristic (ROC) curve analysis was used to determine the diagnostic efficiency of miR-195-5p and miR-211-5p panel. The Kaplan-Meier method was used to assess the prognostic value of plasma exosomal miR-195-5p and miR-211-5p. RESULTS: GC patients possessed notably raised plasma levels of exosomal miR-195-5p and miR-211-5p. The area under ROC curves (AUCs) of miR-195-5p, miR-211-5p were 0.745, 0.798 in the screening phase and 0.762, 0.798 in the training stage respectively. GC was able to be diagnosed more accurately when both miRNAs were interpreted together (AUC=0.820 in the validation stage). Poorer prognosis was observed in GC patients who had plasma exosomal miR-195-5p and miR-211-5p of higher levels. In vitro experiments also confirmed that miR-195-5p and miR-211-5p is able to be transmitted between cells, and works to enhance tumor invasion, migration and proliferation while inhibiting cell apoptosis. CONCLUSION: Plasma exosomal miR-195-5p and miR-211-5p may become potential biomarkers for GC diagnosis, and may be useful in predicting tumor phenotype. Frontiers Media S.A. 2021-08-04 /pmc/articles/PMC8371241/ /pubmed/34422636 http://dx.doi.org/10.3389/fonc.2021.683465 Text en Copyright © 2021 Yang, Li, Wei, Peng, Sang, Jin, Chen, Dang and Zhang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Yang, Jiajia
Li, Xuan
Wei, Shuchun
Peng, Lei
Sang, Huaiming
Jin, Duochen
Chen, Meihong
Dang, Yini
Zhang, Guoxin
Evaluation of the Diagnostic Potential of a Plasma Exosomal miRNAs Panel for Gastric Cancer
title Evaluation of the Diagnostic Potential of a Plasma Exosomal miRNAs Panel for Gastric Cancer
title_full Evaluation of the Diagnostic Potential of a Plasma Exosomal miRNAs Panel for Gastric Cancer
title_fullStr Evaluation of the Diagnostic Potential of a Plasma Exosomal miRNAs Panel for Gastric Cancer
title_full_unstemmed Evaluation of the Diagnostic Potential of a Plasma Exosomal miRNAs Panel for Gastric Cancer
title_short Evaluation of the Diagnostic Potential of a Plasma Exosomal miRNAs Panel for Gastric Cancer
title_sort evaluation of the diagnostic potential of a plasma exosomal mirnas panel for gastric cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8371241/
https://www.ncbi.nlm.nih.gov/pubmed/34422636
http://dx.doi.org/10.3389/fonc.2021.683465
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