Stratification of lncRNA modulation networks in breast cancer

Bibliographic Details
Title: Stratification of lncRNA modulation networks in breast cancer
Authors: Wen-Hsuan Yu, Chia-Lang Hsu, Chen-Ching Lin, Yen-Jen Oyang, Hsueh-Fen Juan, Hsuan-Cheng Huang
Source: BMC Medical Genomics, Vol 14, Iss S3, Pp 1-12 (2022)
Publisher Information: BMC, 2022.
Publication Year: 2022
Collection: LCC:Internal medicine
LCC:Genetics
Subject Terms: Long non-coding RNA, Gene co-expression network, Association network, Breast cancer, Internal medicine, RC31-1245, Genetics, QH426-470
More Details: Abstract Background Recently, non-coding RNAs are of growing interest, and more scientists attach importance to research on their functions. Long non-coding RNAs (lncRNAs) are defined as non-protein coding transcripts longer than 200 nucleotides. We already knew that lncRNAs are related to cancers and will be dysregulated in them. But most of their functions are still left to further study. A mechanism of RNA regulation, known as competing endogenous RNAs (ceRNAs), has been proposed to explain the complex relationships among mRNAs and lncRNAs by competing for binding with shared microRNAs (miRNAs). Methods We proposed an analysis framework to construct the association networks among lncRNA, mRNA, and miRNAs based on their expression patterns and decipher their network modules. Results We collected a large-scale gene expression dataset of 1,061 samples from breast invasive carcinoma (BRCA) patients, each consisted of the expression profiles of 4,359 lncRNAs, 16,517 mRNAs, and 534 miRNAs, and applied the proposed analysis approach to interrogate them. We have uncovered the underlying ceRNA modules and the key modulatory lncRNAs for different subtypes of breast cancer. Conclusions We proposed a modulatory analysis to infer the ceRNA effects among mRNAs and lncRNAs and performed functional analysis to reveal the plausible mechanisms of lncRNA modulation in the four breast cancer subtypes. Our results might provide new directions for breast cancer therapeutics and the proposed method could be readily applied to other diseases.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1755-8794
Relation: https://doaj.org/toc/1755-8794
DOI: 10.1186/s12920-022-01236-6
Access URL: https://doaj.org/article/237fff6bc81242afba8cca2ad1fd089f
Accession Number: edsdoj.237fff6bc81242afba8cca2ad1fd089f
Database: Directory of Open Access Journals
Full text is not displayed to guests.
More Details
ISSN:17558794
DOI:10.1186/s12920-022-01236-6
Published in:BMC Medical Genomics
Language:English