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MicroRNA Expression in Plasma of Esophageal Squamous Cell Carcinoma Patients
BACKGROUND: Patients with esophageal squamous cell carcinoma (ESCC) have a poor prognosis and there are no effective clinical biomarkers. Recently, stable microRNAs detected in the blood have been suggested as potential biomarkers in various cancers. Therefore, we investigated whether plasma microRN...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Academy of Medical Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9247724/ https://www.ncbi.nlm.nih.gov/pubmed/35726148 http://dx.doi.org/10.3346/jkms.2022.37.e197 |
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author | Kahng, Dong Hwahn Kim, Gwang Ha Park, Su Jin Kim, Sora Lee, Moon Won Lee, Bong Eun I, Hoseok |
author_facet | Kahng, Dong Hwahn Kim, Gwang Ha Park, Su Jin Kim, Sora Lee, Moon Won Lee, Bong Eun I, Hoseok |
author_sort | Kahng, Dong Hwahn |
collection | PubMed |
description | BACKGROUND: Patients with esophageal squamous cell carcinoma (ESCC) have a poor prognosis and there are no effective clinical biomarkers. Recently, stable microRNAs detected in the blood have been suggested as potential biomarkers in various cancers. Therefore, we investigated whether plasma microRNAs could be feasible biomarkers for ESCC. METHODS: Peripheral blood samples were obtained from 16 healthy volunteers and 66 ESCC patients before treatment between May 2016 and April 2021. Plasma miR-18b, miR-21, miR-31, and miR-375 expression levels were measured using reverse transcription-quantitative polymerase chain reaction. RESULTS: Compared with those in healthy controls, the expression levels of plasma miR-21 were significantly higher (P = 0.022) and those of plasma miR-31 and miR-375 were significantly lower in ESCC patients (both P < 0.001). Plasma miR-18b expression levels increased in ESCC patients, but the difference was not significant (P = 0.164). The sensitivities and specificities of miR-21, miR-31, and miR-375 for differentiating ESCC patients from healthy controls were 87.5% and 61.9%, 87.5% and 98.4%, and 87.5% and 100%, respectively. There was no difference in expression levels of plasma miR-21, miR-31, and miR-375 according to clinicopathological characteristics of sex, age, tumor size and location, histologic grade, and tumor-node-metastasis stage. CONCLUSION: Our study demonstrated that plasma miR-21, miR-31, and miR-375 could be potential biomarkers for the diagnosis of ESCC. Particularly, plasma miR-31 and miR-375 showed high sensitivity and specificity for differentiating ESCC patients from healthy controls. |
format | Online Article Text |
id | pubmed-9247724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-92477242022-07-06 MicroRNA Expression in Plasma of Esophageal Squamous Cell Carcinoma Patients Kahng, Dong Hwahn Kim, Gwang Ha Park, Su Jin Kim, Sora Lee, Moon Won Lee, Bong Eun I, Hoseok J Korean Med Sci Original Article BACKGROUND: Patients with esophageal squamous cell carcinoma (ESCC) have a poor prognosis and there are no effective clinical biomarkers. Recently, stable microRNAs detected in the blood have been suggested as potential biomarkers in various cancers. Therefore, we investigated whether plasma microRNAs could be feasible biomarkers for ESCC. METHODS: Peripheral blood samples were obtained from 16 healthy volunteers and 66 ESCC patients before treatment between May 2016 and April 2021. Plasma miR-18b, miR-21, miR-31, and miR-375 expression levels were measured using reverse transcription-quantitative polymerase chain reaction. RESULTS: Compared with those in healthy controls, the expression levels of plasma miR-21 were significantly higher (P = 0.022) and those of plasma miR-31 and miR-375 were significantly lower in ESCC patients (both P < 0.001). Plasma miR-18b expression levels increased in ESCC patients, but the difference was not significant (P = 0.164). The sensitivities and specificities of miR-21, miR-31, and miR-375 for differentiating ESCC patients from healthy controls were 87.5% and 61.9%, 87.5% and 98.4%, and 87.5% and 100%, respectively. There was no difference in expression levels of plasma miR-21, miR-31, and miR-375 according to clinicopathological characteristics of sex, age, tumor size and location, histologic grade, and tumor-node-metastasis stage. CONCLUSION: Our study demonstrated that plasma miR-21, miR-31, and miR-375 could be potential biomarkers for the diagnosis of ESCC. Particularly, plasma miR-31 and miR-375 showed high sensitivity and specificity for differentiating ESCC patients from healthy controls. The Korean Academy of Medical Sciences 2022-06-08 /pmc/articles/PMC9247724/ /pubmed/35726148 http://dx.doi.org/10.3346/jkms.2022.37.e197 Text en © 2022 The Korean Academy of Medical Sciences. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kahng, Dong Hwahn Kim, Gwang Ha Park, Su Jin Kim, Sora Lee, Moon Won Lee, Bong Eun I, Hoseok MicroRNA Expression in Plasma of Esophageal Squamous Cell Carcinoma Patients |
title | MicroRNA Expression in Plasma of Esophageal Squamous Cell Carcinoma Patients |
title_full | MicroRNA Expression in Plasma of Esophageal Squamous Cell Carcinoma Patients |
title_fullStr | MicroRNA Expression in Plasma of Esophageal Squamous Cell Carcinoma Patients |
title_full_unstemmed | MicroRNA Expression in Plasma of Esophageal Squamous Cell Carcinoma Patients |
title_short | MicroRNA Expression in Plasma of Esophageal Squamous Cell Carcinoma Patients |
title_sort | microrna expression in plasma of esophageal squamous cell carcinoma patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9247724/ https://www.ncbi.nlm.nih.gov/pubmed/35726148 http://dx.doi.org/10.3346/jkms.2022.37.e197 |
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