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Relationships of circular RNA with diabetes and depression
Type 2 diabetes mellitus (T2DM) is closely related to depression; however, the exact molecular mechnisms of this association are unknown. Here, we investigated whether circular RNAs (circRNAs) in the blood are related to the occurrence of depression in patients with T2DM. Fourteen patients with T2DM...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5544722/ https://www.ncbi.nlm.nih.gov/pubmed/28779132 http://dx.doi.org/10.1038/s41598-017-07931-0 |
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author | Jiang, Guangjian Ma, Yue An, Tian Pan, Yanyun Mo, Fangfang Zhao, Dandan Liu, Yufei Miao, Jia-Nan Gu, Yu-Jie Wang, Yangang Gao, Si-Hua |
author_facet | Jiang, Guangjian Ma, Yue An, Tian Pan, Yanyun Mo, Fangfang Zhao, Dandan Liu, Yufei Miao, Jia-Nan Gu, Yu-Jie Wang, Yangang Gao, Si-Hua |
author_sort | Jiang, Guangjian |
collection | PubMed |
description | Type 2 diabetes mellitus (T2DM) is closely related to depression; however, the exact molecular mechnisms of this association are unknown. Here, we investigated whether circular RNAs (circRNAs) in the blood are related to the occurrence of depression in patients with T2DM. Fourteen patients with T2DM and depressive symptoms, as assessed by the Self-Rating Depression Scale, were included in this study. Cutoff points of 44 (total coarse points) and 55 (standard score) were used to define depression. The Patient Health Questionnaire 9 was used for common mental disorders, and a score of 5 or more the cutoff for depression. Microarray assays and quantitative real-time reverse transcription polymerase chain reaction showed that 183 hsa-circRNAs were significantly upregulated, whereas 64 were downregulated in the T2DM with depression group (p < 0.05) compared with that in the T2DM group. Differentially expressed hsa-circRNAs could interact with microRNAs to target mRNA expression. KEGG pathway analysis predicted that upregulation of hsa-circRNA_003251, hsa-circRNA_015115, hsa-circRNA_100918, and hsa_circRNA_001520 may participate in the thyroid hormone, Wnt, ErbB, and mitogen-activated protein kinase signalling pathways. We speculate that differentially expressed hsa-circRNAs could help us to clarify the pathogenesis of depression in patients with T2DM and could represent novel molecular targets for clinical diagnosis and therapy. |
format | Online Article Text |
id | pubmed-5544722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55447222017-08-09 Relationships of circular RNA with diabetes and depression Jiang, Guangjian Ma, Yue An, Tian Pan, Yanyun Mo, Fangfang Zhao, Dandan Liu, Yufei Miao, Jia-Nan Gu, Yu-Jie Wang, Yangang Gao, Si-Hua Sci Rep Article Type 2 diabetes mellitus (T2DM) is closely related to depression; however, the exact molecular mechnisms of this association are unknown. Here, we investigated whether circular RNAs (circRNAs) in the blood are related to the occurrence of depression in patients with T2DM. Fourteen patients with T2DM and depressive symptoms, as assessed by the Self-Rating Depression Scale, were included in this study. Cutoff points of 44 (total coarse points) and 55 (standard score) were used to define depression. The Patient Health Questionnaire 9 was used for common mental disorders, and a score of 5 or more the cutoff for depression. Microarray assays and quantitative real-time reverse transcription polymerase chain reaction showed that 183 hsa-circRNAs were significantly upregulated, whereas 64 were downregulated in the T2DM with depression group (p < 0.05) compared with that in the T2DM group. Differentially expressed hsa-circRNAs could interact with microRNAs to target mRNA expression. KEGG pathway analysis predicted that upregulation of hsa-circRNA_003251, hsa-circRNA_015115, hsa-circRNA_100918, and hsa_circRNA_001520 may participate in the thyroid hormone, Wnt, ErbB, and mitogen-activated protein kinase signalling pathways. We speculate that differentially expressed hsa-circRNAs could help us to clarify the pathogenesis of depression in patients with T2DM and could represent novel molecular targets for clinical diagnosis and therapy. Nature Publishing Group UK 2017-08-04 /pmc/articles/PMC5544722/ /pubmed/28779132 http://dx.doi.org/10.1038/s41598-017-07931-0 Text en © The Author(s) 2017 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jiang, Guangjian Ma, Yue An, Tian Pan, Yanyun Mo, Fangfang Zhao, Dandan Liu, Yufei Miao, Jia-Nan Gu, Yu-Jie Wang, Yangang Gao, Si-Hua Relationships of circular RNA with diabetes and depression |
title | Relationships of circular RNA with diabetes and depression |
title_full | Relationships of circular RNA with diabetes and depression |
title_fullStr | Relationships of circular RNA with diabetes and depression |
title_full_unstemmed | Relationships of circular RNA with diabetes and depression |
title_short | Relationships of circular RNA with diabetes and depression |
title_sort | relationships of circular rna with diabetes and depression |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5544722/ https://www.ncbi.nlm.nih.gov/pubmed/28779132 http://dx.doi.org/10.1038/s41598-017-07931-0 |
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