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Serum microRNAs as Biomarkers for the Noninvasive Early Diagnosis of Biliary Tract Cancer
BACKGROUND: Biliary tract cancers (BTCs) are aggressive malignancies with difficult early diagnosis and poor prognosis. Studies have shown that microRNAs (miRNAs) are expected to be biomarkers of the disease, which indicates that we can diagnose cancers according to the miRNAs that have significant...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8021261/ https://www.ncbi.nlm.nih.gov/pubmed/33833559 http://dx.doi.org/10.2147/IJGM.S297371 |
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author | Han, Yueting Zhang, Haiyang Zhou, Zhengyang Liu, Rui Liu, Dongying Bai, Ming Fan, Qian Li, Jialu Zhu, Kegan Li, Hongli Ning, Tao Ying, Guoguang Ba, Yi |
author_facet | Han, Yueting Zhang, Haiyang Zhou, Zhengyang Liu, Rui Liu, Dongying Bai, Ming Fan, Qian Li, Jialu Zhu, Kegan Li, Hongli Ning, Tao Ying, Guoguang Ba, Yi |
author_sort | Han, Yueting |
collection | PubMed |
description | BACKGROUND: Biliary tract cancers (BTCs) are aggressive malignancies with difficult early diagnosis and poor prognosis. Studies have shown that microRNAs (miRNAs) are expected to be biomarkers of the disease, which indicates that we can diagnose cancers according to the miRNAs that have significant changes. The aim of this study was to explore miRNA biomarkers of BTCs. METHODS: A total of 163 samples were collected and divided into the control group, the benign group and the malignant group. High-throughput low-density chips were used to screen miRNAs with significant changes. Then, the preliminary screening test and the verification test were performed by quantitative real time PCR (qRT-PCR). Finally, the level of miRNAs in serum exosomes was measured. RESULTS: MiR-10a, miR-21, miR-135b, miR-221, and miR-214 were upregulated in the BTCs group compared to the control group. The change in the miR-221 level was statistically significant when the malignant group was compared with the benign group (P<0.01). Meanwhile, miR-135b and miR-214 were enriched in serum exosomes. CONCLUSION: Five miRNAs in the serum were found to be significantly upregulated in patients with BTCs. Among them, miR-221 can serve as an early diagnostic marker for BTCs patients. MiR-10a, miR-21, miR-135b and miR-214 can be used as biomarkers for the diagnosis of biliary diseases. |
format | Online Article Text |
id | pubmed-8021261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-80212612021-04-07 Serum microRNAs as Biomarkers for the Noninvasive Early Diagnosis of Biliary Tract Cancer Han, Yueting Zhang, Haiyang Zhou, Zhengyang Liu, Rui Liu, Dongying Bai, Ming Fan, Qian Li, Jialu Zhu, Kegan Li, Hongli Ning, Tao Ying, Guoguang Ba, Yi Int J Gen Med Original Research BACKGROUND: Biliary tract cancers (BTCs) are aggressive malignancies with difficult early diagnosis and poor prognosis. Studies have shown that microRNAs (miRNAs) are expected to be biomarkers of the disease, which indicates that we can diagnose cancers according to the miRNAs that have significant changes. The aim of this study was to explore miRNA biomarkers of BTCs. METHODS: A total of 163 samples were collected and divided into the control group, the benign group and the malignant group. High-throughput low-density chips were used to screen miRNAs with significant changes. Then, the preliminary screening test and the verification test were performed by quantitative real time PCR (qRT-PCR). Finally, the level of miRNAs in serum exosomes was measured. RESULTS: MiR-10a, miR-21, miR-135b, miR-221, and miR-214 were upregulated in the BTCs group compared to the control group. The change in the miR-221 level was statistically significant when the malignant group was compared with the benign group (P<0.01). Meanwhile, miR-135b and miR-214 were enriched in serum exosomes. CONCLUSION: Five miRNAs in the serum were found to be significantly upregulated in patients with BTCs. Among them, miR-221 can serve as an early diagnostic marker for BTCs patients. MiR-10a, miR-21, miR-135b and miR-214 can be used as biomarkers for the diagnosis of biliary diseases. Dove 2021-04-01 /pmc/articles/PMC8021261/ /pubmed/33833559 http://dx.doi.org/10.2147/IJGM.S297371 Text en © 2021 Han et al. https://creativecommons.org/licenses/by-nc/3.0/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/ (https://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. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Han, Yueting Zhang, Haiyang Zhou, Zhengyang Liu, Rui Liu, Dongying Bai, Ming Fan, Qian Li, Jialu Zhu, Kegan Li, Hongli Ning, Tao Ying, Guoguang Ba, Yi Serum microRNAs as Biomarkers for the Noninvasive Early Diagnosis of Biliary Tract Cancer |
title | Serum microRNAs as Biomarkers for the Noninvasive Early Diagnosis of Biliary Tract Cancer |
title_full | Serum microRNAs as Biomarkers for the Noninvasive Early Diagnosis of Biliary Tract Cancer |
title_fullStr | Serum microRNAs as Biomarkers for the Noninvasive Early Diagnosis of Biliary Tract Cancer |
title_full_unstemmed | Serum microRNAs as Biomarkers for the Noninvasive Early Diagnosis of Biliary Tract Cancer |
title_short | Serum microRNAs as Biomarkers for the Noninvasive Early Diagnosis of Biliary Tract Cancer |
title_sort | serum micrornas as biomarkers for the noninvasive early diagnosis of biliary tract cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8021261/ https://www.ncbi.nlm.nih.gov/pubmed/33833559 http://dx.doi.org/10.2147/IJGM.S297371 |
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