Cargando…
dbDEMC 3.0: Functional Exploration of Differentially Expressed miRNAs in Cancers of Human and Model Organisms
MicroRNAs (miRNAs) are important regulators in gene expression. The dysregulation of miRNA expression is widely reported in the transformation from physiological to pathological states of cells. A large number of differentially expressed miRNAs (DEMs) have been identified in various human cancers by...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9801039/ https://www.ncbi.nlm.nih.gov/pubmed/35643191 http://dx.doi.org/10.1016/j.gpb.2022.04.006 |
_version_ | 1784861414932873216 |
---|---|
author | Xu, Feng Wang, Yifan Ling, Yunchao Zhou, Chenfen Wang, Haizhou Teschendorff, Andrew E. Zhao, Yi Zhao, Haitao He, Yungang Zhang, Guoqing Yang, Zhen |
author_facet | Xu, Feng Wang, Yifan Ling, Yunchao Zhou, Chenfen Wang, Haizhou Teschendorff, Andrew E. Zhao, Yi Zhao, Haitao He, Yungang Zhang, Guoqing Yang, Zhen |
author_sort | Xu, Feng |
collection | PubMed |
description | MicroRNAs (miRNAs) are important regulators in gene expression. The dysregulation of miRNA expression is widely reported in the transformation from physiological to pathological states of cells. A large number of differentially expressed miRNAs (DEMs) have been identified in various human cancers by using high-throughput technologies, such as microarray and miRNA-seq. Through mining of published studies with high-throughput experiment information, the database of DEMs in human cancers (dbDEMC) was constructed with the aim of providing a systematic resource for the storage and query of the DEMs. Here we report an update of the dbDEMC to version 3.0, which contains two-fold more data entries than the second version and now includes also data from mice and rats. The dbDEMC 3.0 contains 3268 unique DEMs in 40 different cancer types. The current datasets for differential expression analysis have expanded to 9 generalized categories. Moreover, the current release integrates functional annotations of DEMs obtained by using experimentally validated targets. The annotations can be of great benefit to the intensive analysis of the roles of DEMs in cancer. In summary, dbDEMC 3.0 provides a valuable resource for characterizing molecular functions and regulatory mechanisms of DEMs in human cancers. The dbDEMC 3.0 is freely accessible at https://www.biosino.org/dbDEMC. |
format | Online Article Text |
id | pubmed-9801039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-98010392022-12-31 dbDEMC 3.0: Functional Exploration of Differentially Expressed miRNAs in Cancers of Human and Model Organisms Xu, Feng Wang, Yifan Ling, Yunchao Zhou, Chenfen Wang, Haizhou Teschendorff, Andrew E. Zhao, Yi Zhao, Haitao He, Yungang Zhang, Guoqing Yang, Zhen Genomics Proteomics Bioinformatics Database MicroRNAs (miRNAs) are important regulators in gene expression. The dysregulation of miRNA expression is widely reported in the transformation from physiological to pathological states of cells. A large number of differentially expressed miRNAs (DEMs) have been identified in various human cancers by using high-throughput technologies, such as microarray and miRNA-seq. Through mining of published studies with high-throughput experiment information, the database of DEMs in human cancers (dbDEMC) was constructed with the aim of providing a systematic resource for the storage and query of the DEMs. Here we report an update of the dbDEMC to version 3.0, which contains two-fold more data entries than the second version and now includes also data from mice and rats. The dbDEMC 3.0 contains 3268 unique DEMs in 40 different cancer types. The current datasets for differential expression analysis have expanded to 9 generalized categories. Moreover, the current release integrates functional annotations of DEMs obtained by using experimentally validated targets. The annotations can be of great benefit to the intensive analysis of the roles of DEMs in cancer. In summary, dbDEMC 3.0 provides a valuable resource for characterizing molecular functions and regulatory mechanisms of DEMs in human cancers. The dbDEMC 3.0 is freely accessible at https://www.biosino.org/dbDEMC. Elsevier 2022-06 2022-05-25 /pmc/articles/PMC9801039/ /pubmed/35643191 http://dx.doi.org/10.1016/j.gpb.2022.04.006 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Database Xu, Feng Wang, Yifan Ling, Yunchao Zhou, Chenfen Wang, Haizhou Teschendorff, Andrew E. Zhao, Yi Zhao, Haitao He, Yungang Zhang, Guoqing Yang, Zhen dbDEMC 3.0: Functional Exploration of Differentially Expressed miRNAs in Cancers of Human and Model Organisms |
title | dbDEMC 3.0: Functional Exploration of Differentially Expressed miRNAs in Cancers of Human and Model Organisms |
title_full | dbDEMC 3.0: Functional Exploration of Differentially Expressed miRNAs in Cancers of Human and Model Organisms |
title_fullStr | dbDEMC 3.0: Functional Exploration of Differentially Expressed miRNAs in Cancers of Human and Model Organisms |
title_full_unstemmed | dbDEMC 3.0: Functional Exploration of Differentially Expressed miRNAs in Cancers of Human and Model Organisms |
title_short | dbDEMC 3.0: Functional Exploration of Differentially Expressed miRNAs in Cancers of Human and Model Organisms |
title_sort | dbdemc 3.0: functional exploration of differentially expressed mirnas in cancers of human and model organisms |
topic | Database |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9801039/ https://www.ncbi.nlm.nih.gov/pubmed/35643191 http://dx.doi.org/10.1016/j.gpb.2022.04.006 |
work_keys_str_mv | AT xufeng dbdemc30functionalexplorationofdifferentiallyexpressedmirnasincancersofhumanandmodelorganisms AT wangyifan dbdemc30functionalexplorationofdifferentiallyexpressedmirnasincancersofhumanandmodelorganisms AT lingyunchao dbdemc30functionalexplorationofdifferentiallyexpressedmirnasincancersofhumanandmodelorganisms AT zhouchenfen dbdemc30functionalexplorationofdifferentiallyexpressedmirnasincancersofhumanandmodelorganisms AT wanghaizhou dbdemc30functionalexplorationofdifferentiallyexpressedmirnasincancersofhumanandmodelorganisms AT teschendorffandrewe dbdemc30functionalexplorationofdifferentiallyexpressedmirnasincancersofhumanandmodelorganisms AT zhaoyi dbdemc30functionalexplorationofdifferentiallyexpressedmirnasincancersofhumanandmodelorganisms AT zhaohaitao dbdemc30functionalexplorationofdifferentiallyexpressedmirnasincancersofhumanandmodelorganisms AT heyungang dbdemc30functionalexplorationofdifferentiallyexpressedmirnasincancersofhumanandmodelorganisms AT zhangguoqing dbdemc30functionalexplorationofdifferentiallyexpressedmirnasincancersofhumanandmodelorganisms AT yangzhen dbdemc30functionalexplorationofdifferentiallyexpressedmirnasincancersofhumanandmodelorganisms |