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Serum miR‐92a‐1 is a novel diagnostic biomarker for colorectal cancer
Colorectal cancer (CRC) is one of the most common cancers worldwide, with high mortality. Abnormally expressed microRNAs (miRNAs) are considered novel biomarkers in cancer diagnosis. The aim of this study was to investigate the diagnostic value of miR‐92a‐1 in patients with CRC. Serum samples were c...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7412696/ https://www.ncbi.nlm.nih.gov/pubmed/32562465 http://dx.doi.org/10.1111/jcmm.15282 |
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author | Shi, Ying Liu, Zhibao |
author_facet | Shi, Ying Liu, Zhibao |
author_sort | Shi, Ying |
collection | PubMed |
description | Colorectal cancer (CRC) is one of the most common cancers worldwide, with high mortality. Abnormally expressed microRNAs (miRNAs) are considered novel biomarkers in cancer diagnosis. The aim of this study was to investigate the diagnostic value of miR‐92a‐1 in patients with CRC. Serum samples were collected from 148 patients pathologically diagnosed with CRC and 68 gender‐ and age‐matched healthy volunteers. Quantitative real‐time polymerase chain reaction (qRT‐PCR) was used to measure serum miR‐92a‐1 level. Relationship between miR‐92a‐1 and clinicopathological features of CRC cases was analysed via chi‐square test. Receiver operating characteristic (ROC) curve was plotted to estimate the diagnostic value of miR‐92a‐1 in CRC. Serum miR‐92a‐1 was significantly up‐regulated in CRC patients compared with healthy individuals (P < .001). Moreover, miR‐92a‐1 expression was correlated with TNM stage (P = .02), histological stage (P = .003), lymph node metastasis (P = .003) and distant metastasis (P < .001). ROC analysis showed that the area under the ROC curve (AUC) was 0.914, suggesting high diagnostic accuracy of miR‐92a‐1 in ROC. The optimal cut‐off value was 1.485, with a sensitivity of 81.8% and a specificity of 95.6%. MiR‐92a‐1 is increased in CRC patients and correlated with aggressive clinical characteristics. Serum miR‐92a‐1 may be a potential diagnostic biomarker for CRC. |
format | Online Article Text |
id | pubmed-7412696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74126962020-08-10 Serum miR‐92a‐1 is a novel diagnostic biomarker for colorectal cancer Shi, Ying Liu, Zhibao J Cell Mol Med Original Articles Colorectal cancer (CRC) is one of the most common cancers worldwide, with high mortality. Abnormally expressed microRNAs (miRNAs) are considered novel biomarkers in cancer diagnosis. The aim of this study was to investigate the diagnostic value of miR‐92a‐1 in patients with CRC. Serum samples were collected from 148 patients pathologically diagnosed with CRC and 68 gender‐ and age‐matched healthy volunteers. Quantitative real‐time polymerase chain reaction (qRT‐PCR) was used to measure serum miR‐92a‐1 level. Relationship between miR‐92a‐1 and clinicopathological features of CRC cases was analysed via chi‐square test. Receiver operating characteristic (ROC) curve was plotted to estimate the diagnostic value of miR‐92a‐1 in CRC. Serum miR‐92a‐1 was significantly up‐regulated in CRC patients compared with healthy individuals (P < .001). Moreover, miR‐92a‐1 expression was correlated with TNM stage (P = .02), histological stage (P = .003), lymph node metastasis (P = .003) and distant metastasis (P < .001). ROC analysis showed that the area under the ROC curve (AUC) was 0.914, suggesting high diagnostic accuracy of miR‐92a‐1 in ROC. The optimal cut‐off value was 1.485, with a sensitivity of 81.8% and a specificity of 95.6%. MiR‐92a‐1 is increased in CRC patients and correlated with aggressive clinical characteristics. Serum miR‐92a‐1 may be a potential diagnostic biomarker for CRC. John Wiley and Sons Inc. 2020-06-20 2020-08 /pmc/articles/PMC7412696/ /pubmed/32562465 http://dx.doi.org/10.1111/jcmm.15282 Text en © 2020 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Shi, Ying Liu, Zhibao Serum miR‐92a‐1 is a novel diagnostic biomarker for colorectal cancer |
title | Serum miR‐92a‐1 is a novel diagnostic biomarker for colorectal cancer |
title_full | Serum miR‐92a‐1 is a novel diagnostic biomarker for colorectal cancer |
title_fullStr | Serum miR‐92a‐1 is a novel diagnostic biomarker for colorectal cancer |
title_full_unstemmed | Serum miR‐92a‐1 is a novel diagnostic biomarker for colorectal cancer |
title_short | Serum miR‐92a‐1 is a novel diagnostic biomarker for colorectal cancer |
title_sort | serum mir‐92a‐1 is a novel diagnostic biomarker for colorectal cancer |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7412696/ https://www.ncbi.nlm.nih.gov/pubmed/32562465 http://dx.doi.org/10.1111/jcmm.15282 |
work_keys_str_mv | AT shiying serummir92a1isanoveldiagnosticbiomarkerforcolorectalcancer AT liuzhibao serummir92a1isanoveldiagnosticbiomarkerforcolorectalcancer |