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Identification of circular RNAs as a promising new class of diagnostic biomarkers for human breast cancer
Endogenous noncoding circular RNAs (circRNAs) have gained attention for their involvement in carcinogenesis, but their expression pattern in breast cancer has remained largely unknown. In this two-stage study, we first used an Arraystar Human circRNA Array to construct a genome-wide circRNA profile....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5546465/ https://www.ncbi.nlm.nih.gov/pubmed/28484086 http://dx.doi.org/10.18632/oncotarget.17307 |
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author | Lü, Lingshuang Sun, Jian Shi, Peiyi Kong, Weimin Xu, Kun He, Biyu Zhang, Simin Wang, Jianming |
author_facet | Lü, Lingshuang Sun, Jian Shi, Peiyi Kong, Weimin Xu, Kun He, Biyu Zhang, Simin Wang, Jianming |
author_sort | Lü, Lingshuang |
collection | PubMed |
description | Endogenous noncoding circular RNAs (circRNAs) have gained attention for their involvement in carcinogenesis, but their expression pattern in breast cancer has remained largely unknown. In this two-stage study, we first used an Arraystar Human circRNA Array to construct a genome-wide circRNA profile. We then selected candidate circRNAs for validation using a quantitative real-time polymerase chain reaction system. CircRNA/miRNA interactions were predicted and sequence analyses were performed. Among 1155 differentially expressed circRNAs, 715 were upregulated and 440 were downregulated in breast cancer tissues. The validation study demonstrated that hsa_circ_103110, hsa_circ_104689 and hsa_circ_104821 levels were elevated in breast cancer tissues, whereas hsa_circ_006054, hsa_circ_100219 and hsa_circ_406697 were downregulated. These circRNAs targeted complementary miRNA response elements. The area under the receiver operating characteristic curve for distinguishing breast cancer was 0.82 (95% CI: 0.73-0.90) when hsa_circ_006054, hsa_circ_100219 and hsa_circ_406697 were used in combination. This study provides evidence that circRNAs are differentially expressed in breast cancer and are important in carcinogenesis because they participate in cancer-related pathways and sequester miRNAs. |
format | Online Article Text |
id | pubmed-5546465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-55464652017-08-23 Identification of circular RNAs as a promising new class of diagnostic biomarkers for human breast cancer Lü, Lingshuang Sun, Jian Shi, Peiyi Kong, Weimin Xu, Kun He, Biyu Zhang, Simin Wang, Jianming Oncotarget Research Paper Endogenous noncoding circular RNAs (circRNAs) have gained attention for their involvement in carcinogenesis, but their expression pattern in breast cancer has remained largely unknown. In this two-stage study, we first used an Arraystar Human circRNA Array to construct a genome-wide circRNA profile. We then selected candidate circRNAs for validation using a quantitative real-time polymerase chain reaction system. CircRNA/miRNA interactions were predicted and sequence analyses were performed. Among 1155 differentially expressed circRNAs, 715 were upregulated and 440 were downregulated in breast cancer tissues. The validation study demonstrated that hsa_circ_103110, hsa_circ_104689 and hsa_circ_104821 levels were elevated in breast cancer tissues, whereas hsa_circ_006054, hsa_circ_100219 and hsa_circ_406697 were downregulated. These circRNAs targeted complementary miRNA response elements. The area under the receiver operating characteristic curve for distinguishing breast cancer was 0.82 (95% CI: 0.73-0.90) when hsa_circ_006054, hsa_circ_100219 and hsa_circ_406697 were used in combination. This study provides evidence that circRNAs are differentially expressed in breast cancer and are important in carcinogenesis because they participate in cancer-related pathways and sequester miRNAs. Impact Journals LLC 2017-04-21 /pmc/articles/PMC5546465/ /pubmed/28484086 http://dx.doi.org/10.18632/oncotarget.17307 Text en Copyright: © 2017 Lü et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Lü, Lingshuang Sun, Jian Shi, Peiyi Kong, Weimin Xu, Kun He, Biyu Zhang, Simin Wang, Jianming Identification of circular RNAs as a promising new class of diagnostic biomarkers for human breast cancer |
title | Identification of circular RNAs as a promising new class of diagnostic biomarkers for human breast cancer |
title_full | Identification of circular RNAs as a promising new class of diagnostic biomarkers for human breast cancer |
title_fullStr | Identification of circular RNAs as a promising new class of diagnostic biomarkers for human breast cancer |
title_full_unstemmed | Identification of circular RNAs as a promising new class of diagnostic biomarkers for human breast cancer |
title_short | Identification of circular RNAs as a promising new class of diagnostic biomarkers for human breast cancer |
title_sort | identification of circular rnas as a promising new class of diagnostic biomarkers for human breast cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5546465/ https://www.ncbi.nlm.nih.gov/pubmed/28484086 http://dx.doi.org/10.18632/oncotarget.17307 |
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