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Plasma exosomal hsa_circ_0079439 as a novel biomarker for early detection of gastric cancer

BACKGROUND: Due to the poor prognosis of gastric cancer (GC), early detection methods are urgently needed. Plasma exosomal circular RNAs (circRNAs) have been suggested as novel biomarkers for GC. AIM: To identify a novel biomarker for early detection of GC. METHODS: Healthy donors (HDs) and GC patie...

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Autores principales: Li, Xiao, Lin, Yan-Li, Shao, Jia-Kang, Wu, Xiao-Jie, Li, Xiang, Yao, He, Shi, Fa-Liang, Li, Long-Song, Zhang, Wen-Gang, Chang, Zheng-Yao, Chai, Ning-Li, Wang, You-Liang, Linghu, En-Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10303519/
https://www.ncbi.nlm.nih.gov/pubmed/37389236
http://dx.doi.org/10.3748/wjg.v29.i22.3482
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author Li, Xiao
Lin, Yan-Li
Shao, Jia-Kang
Wu, Xiao-Jie
Li, Xiang
Yao, He
Shi, Fa-Liang
Li, Long-Song
Zhang, Wen-Gang
Chang, Zheng-Yao
Chai, Ning-Li
Wang, You-Liang
Linghu, En-Qiang
author_facet Li, Xiao
Lin, Yan-Li
Shao, Jia-Kang
Wu, Xiao-Jie
Li, Xiang
Yao, He
Shi, Fa-Liang
Li, Long-Song
Zhang, Wen-Gang
Chang, Zheng-Yao
Chai, Ning-Li
Wang, You-Liang
Linghu, En-Qiang
author_sort Li, Xiao
collection PubMed
description BACKGROUND: Due to the poor prognosis of gastric cancer (GC), early detection methods are urgently needed. Plasma exosomal circular RNAs (circRNAs) have been suggested as novel biomarkers for GC. AIM: To identify a novel biomarker for early detection of GC. METHODS: Healthy donors (HDs) and GC patients diagnosed by pathology were recruited. Nine GC patients and three HDs were selected for exosomal whole-transcriptome RNA sequencing. The expression profiles of circRNAs were analyzed by bioinformatics methods and validated by droplet digital polymerase chain reaction. The expression levels and area under receiver operating characteristic curve values of plasma exosomal circRNAs and standard serum biomarkers were used to compare their diagnostic efficiency. RESULTS: There were 303 participants, including 240 GC patients and 63 HDs, involved in the study. The expression levels of exosomal hsa_circ_0079439 were significantly higher in GC patients than in HDs (P < 0.0001). However, the levels of standard serum biomarkers were similar between the two groups. The area under the curve value of exosomal hsa_circ_0079439 was higher than those of standard biomarkers, including carcinoembryonic antigen, carbohydrate antigen (CA)19-9, CA72-4, alpha-fetoprotein, and CA125 (0.8595 vs 0.5862, 0.5660, 0.5360, 0.5082, and 0.5018, respectively). The expression levels of exosomal hsa_circ_0079439 were significantly decreased after treatment (P < 0.05). Moreover, the expression levels of exosomal hsa_circ_0079439 were obviously higher in early GC (EGC) patients than in HDs (P < 0.0001). CONCLUSION: Our results suggest that plasma exosomal hsa_circ_0079439 is upregulated in GC patients. Moreover, the levels of exosomal hsa_circ_0079439 could distinguish EGC and advanced GC patients from HDs. Therefore, plasma exosomal hsa_circ_0079439 might be a potential biomarker for the diagnosis of GC during both the early and late stages.
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spelling pubmed-103035192023-06-29 Plasma exosomal hsa_circ_0079439 as a novel biomarker for early detection of gastric cancer Li, Xiao Lin, Yan-Li Shao, Jia-Kang Wu, Xiao-Jie Li, Xiang Yao, He Shi, Fa-Liang Li, Long-Song Zhang, Wen-Gang Chang, Zheng-Yao Chai, Ning-Li Wang, You-Liang Linghu, En-Qiang World J Gastroenterol Case Control Study BACKGROUND: Due to the poor prognosis of gastric cancer (GC), early detection methods are urgently needed. Plasma exosomal circular RNAs (circRNAs) have been suggested as novel biomarkers for GC. AIM: To identify a novel biomarker for early detection of GC. METHODS: Healthy donors (HDs) and GC patients diagnosed by pathology were recruited. Nine GC patients and three HDs were selected for exosomal whole-transcriptome RNA sequencing. The expression profiles of circRNAs were analyzed by bioinformatics methods and validated by droplet digital polymerase chain reaction. The expression levels and area under receiver operating characteristic curve values of plasma exosomal circRNAs and standard serum biomarkers were used to compare their diagnostic efficiency. RESULTS: There were 303 participants, including 240 GC patients and 63 HDs, involved in the study. The expression levels of exosomal hsa_circ_0079439 were significantly higher in GC patients than in HDs (P < 0.0001). However, the levels of standard serum biomarkers were similar between the two groups. The area under the curve value of exosomal hsa_circ_0079439 was higher than those of standard biomarkers, including carcinoembryonic antigen, carbohydrate antigen (CA)19-9, CA72-4, alpha-fetoprotein, and CA125 (0.8595 vs 0.5862, 0.5660, 0.5360, 0.5082, and 0.5018, respectively). The expression levels of exosomal hsa_circ_0079439 were significantly decreased after treatment (P < 0.05). Moreover, the expression levels of exosomal hsa_circ_0079439 were obviously higher in early GC (EGC) patients than in HDs (P < 0.0001). CONCLUSION: Our results suggest that plasma exosomal hsa_circ_0079439 is upregulated in GC patients. Moreover, the levels of exosomal hsa_circ_0079439 could distinguish EGC and advanced GC patients from HDs. Therefore, plasma exosomal hsa_circ_0079439 might be a potential biomarker for the diagnosis of GC during both the early and late stages. Baishideng Publishing Group Inc 2023-06-14 2023-06-14 /pmc/articles/PMC10303519/ /pubmed/37389236 http://dx.doi.org/10.3748/wjg.v29.i22.3482 Text en ©The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Case Control Study
Li, Xiao
Lin, Yan-Li
Shao, Jia-Kang
Wu, Xiao-Jie
Li, Xiang
Yao, He
Shi, Fa-Liang
Li, Long-Song
Zhang, Wen-Gang
Chang, Zheng-Yao
Chai, Ning-Li
Wang, You-Liang
Linghu, En-Qiang
Plasma exosomal hsa_circ_0079439 as a novel biomarker for early detection of gastric cancer
title Plasma exosomal hsa_circ_0079439 as a novel biomarker for early detection of gastric cancer
title_full Plasma exosomal hsa_circ_0079439 as a novel biomarker for early detection of gastric cancer
title_fullStr Plasma exosomal hsa_circ_0079439 as a novel biomarker for early detection of gastric cancer
title_full_unstemmed Plasma exosomal hsa_circ_0079439 as a novel biomarker for early detection of gastric cancer
title_short Plasma exosomal hsa_circ_0079439 as a novel biomarker for early detection of gastric cancer
title_sort plasma exosomal hsa_circ_0079439 as a novel biomarker for early detection of gastric cancer
topic Case Control Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10303519/
https://www.ncbi.nlm.nih.gov/pubmed/37389236
http://dx.doi.org/10.3748/wjg.v29.i22.3482
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