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Plasma circRNA microarray profiling identifies novel circRNA biomarkers for the diagnosis of ovarian cancer
BACKGROUND: Circular RNA (circRNA), a class of RNA with a covalent closed circular structure that widely existed in serum and plasma, has been considered an ideal liquid biopsy marker in many diseases. In this study, we employed microarray and qRT-PCR to evaluate the potential circulating circRNAs w...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9097182/ https://www.ncbi.nlm.nih.gov/pubmed/35550610 http://dx.doi.org/10.1186/s13048-022-00988-0 |
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author | Ge, Lili Sun, Yu Shi, Yaqian Liu, Guangquan Teng, Fang Geng, Zhe Chen, Xiyi Xu, Hanzi Xu, Juan Jia, Xuemei |
author_facet | Ge, Lili Sun, Yu Shi, Yaqian Liu, Guangquan Teng, Fang Geng, Zhe Chen, Xiyi Xu, Hanzi Xu, Juan Jia, Xuemei |
author_sort | Ge, Lili |
collection | PubMed |
description | BACKGROUND: Circular RNA (circRNA), a class of RNA with a covalent closed circular structure that widely existed in serum and plasma, has been considered an ideal liquid biopsy marker in many diseases. In this study, we employed microarray and qRT-PCR to evaluate the potential circulating circRNAs with diagnostic efficacy in ovarian cancer. METHODS: We used microarray to explore the circRNA expression profile in ovarian cancer patients’ plasma and quantitative real-time (qRT)-PCR approach to assessing the candidate circRNA’s expression. Then the receiver operating characteristic (ROC) curve was employed to analyze the diagnostic values of candidate circRNAs. The diagnostic model circCOMBO was a combination of hsa_circ_0003972 and hsa_circ_0007288 built by binary logistic regression. Then bioinformatic tools were used to predict their potential mechanisms. RESULTS: Hsa_circ_0003972 and hsa_circ_0007288 were downregulated in ovarian cancer patients’ plasma, tissues, and cell lines, comparing with the controls. Hsa_circ_0003972 and hsa_circ_0007288 exhibited diagnostic values with the Area Under Curve (AUC) of 0.724 and 0.790, respectively. circCOMBO showed a better diagnostic utility (AUC: 0.781), while the combination of circCOMBO and carbohydrate antigen 125 (CA125) showed the highest diagnostic value (AUC: 0.923). Furthermore, the higher expression level of hsa_circ_0007288 in both plasma and ovarian cancer tissues was associated with lower lymph node metastasis potential in ovarian cancer. CONCLUSIONS: Our results revealed that hsa_circ_0003972 and hsa_circ_0007288 may serve as novel circulating biomarkers for ovarian cancer diagnosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13048-022-00988-0. |
format | Online Article Text |
id | pubmed-9097182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-90971822022-05-13 Plasma circRNA microarray profiling identifies novel circRNA biomarkers for the diagnosis of ovarian cancer Ge, Lili Sun, Yu Shi, Yaqian Liu, Guangquan Teng, Fang Geng, Zhe Chen, Xiyi Xu, Hanzi Xu, Juan Jia, Xuemei J Ovarian Res Research BACKGROUND: Circular RNA (circRNA), a class of RNA with a covalent closed circular structure that widely existed in serum and plasma, has been considered an ideal liquid biopsy marker in many diseases. In this study, we employed microarray and qRT-PCR to evaluate the potential circulating circRNAs with diagnostic efficacy in ovarian cancer. METHODS: We used microarray to explore the circRNA expression profile in ovarian cancer patients’ plasma and quantitative real-time (qRT)-PCR approach to assessing the candidate circRNA’s expression. Then the receiver operating characteristic (ROC) curve was employed to analyze the diagnostic values of candidate circRNAs. The diagnostic model circCOMBO was a combination of hsa_circ_0003972 and hsa_circ_0007288 built by binary logistic regression. Then bioinformatic tools were used to predict their potential mechanisms. RESULTS: Hsa_circ_0003972 and hsa_circ_0007288 were downregulated in ovarian cancer patients’ plasma, tissues, and cell lines, comparing with the controls. Hsa_circ_0003972 and hsa_circ_0007288 exhibited diagnostic values with the Area Under Curve (AUC) of 0.724 and 0.790, respectively. circCOMBO showed a better diagnostic utility (AUC: 0.781), while the combination of circCOMBO and carbohydrate antigen 125 (CA125) showed the highest diagnostic value (AUC: 0.923). Furthermore, the higher expression level of hsa_circ_0007288 in both plasma and ovarian cancer tissues was associated with lower lymph node metastasis potential in ovarian cancer. CONCLUSIONS: Our results revealed that hsa_circ_0003972 and hsa_circ_0007288 may serve as novel circulating biomarkers for ovarian cancer diagnosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13048-022-00988-0. BioMed Central 2022-05-12 /pmc/articles/PMC9097182/ /pubmed/35550610 http://dx.doi.org/10.1186/s13048-022-00988-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ge, Lili Sun, Yu Shi, Yaqian Liu, Guangquan Teng, Fang Geng, Zhe Chen, Xiyi Xu, Hanzi Xu, Juan Jia, Xuemei Plasma circRNA microarray profiling identifies novel circRNA biomarkers for the diagnosis of ovarian cancer |
title | Plasma circRNA microarray profiling identifies novel circRNA biomarkers for the diagnosis of ovarian cancer |
title_full | Plasma circRNA microarray profiling identifies novel circRNA biomarkers for the diagnosis of ovarian cancer |
title_fullStr | Plasma circRNA microarray profiling identifies novel circRNA biomarkers for the diagnosis of ovarian cancer |
title_full_unstemmed | Plasma circRNA microarray profiling identifies novel circRNA biomarkers for the diagnosis of ovarian cancer |
title_short | Plasma circRNA microarray profiling identifies novel circRNA biomarkers for the diagnosis of ovarian cancer |
title_sort | plasma circrna microarray profiling identifies novel circrna biomarkers for the diagnosis of ovarian cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9097182/ https://www.ncbi.nlm.nih.gov/pubmed/35550610 http://dx.doi.org/10.1186/s13048-022-00988-0 |
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