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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...

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Autores principales: Ge, Lili, Sun, Yu, Shi, Yaqian, Liu, Guangquan, Teng, Fang, Geng, Zhe, Chen, Xiyi, Xu, Hanzi, Xu, Juan, Jia, Xuemei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
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.
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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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