Integrated analyses of long noncoding RNAs and mRNAs in the progression of breast cancer

Objective The objective was to explore the expression and potential functions of long noncoding RNA (lncRNA) and mRNAs in human breast cancer (BC). Methods Differentially expressed lncRNAs and mRNAs were identified and annotated in BC tissues by using the Agilent human lncRNA assay (Agilent Technolo...

Full description

Bibliographic Details
Main Authors: Jingyun Guo, Huining Lian, Minfeng Liu, Jianyu Dong, Zhaoze Guo, Jinlamao Yang, Changsheng Ye
Format: Article
Language:English
Published: SAGE Publishing 2021-09-01
Series:Journal of International Medical Research
Online Access:https://doi.org/10.1177/0300060520973137
_version_ 1818596146504794112
author Jingyun Guo
Huining Lian
Minfeng Liu
Jianyu Dong
Zhaoze Guo
Jinlamao Yang
Changsheng Ye
author_facet Jingyun Guo
Huining Lian
Minfeng Liu
Jianyu Dong
Zhaoze Guo
Jinlamao Yang
Changsheng Ye
author_sort Jingyun Guo
collection DOAJ
description Objective The objective was to explore the expression and potential functions of long noncoding RNA (lncRNA) and mRNAs in human breast cancer (BC). Methods Differentially expressed lncRNAs and mRNAs were identified and annotated in BC tissues by using the Agilent human lncRNA assay (Agilent Technologies, Santa Clara, CA, USA) and RNA sequencing. After identification of lncRNAs and mRNAs through quantitative reverse transcription polymerase chain reaction, we conducted a series of functional experiments to confirm the effects of knockdown of one lncRNA, TCONS_00029809, on the progression of BC. Results We discovered 238 lncRNAs and 200 mRNAs that were differentially expressed in BC tissues and para-carcinoma tissue. We showed that differentially expressed mRNAs were related to biological adhesion and biological regulation and mainly enriched in cytokine-cytokine receptor interaction, metabolic pathways, and PI3K-Akt signaling pathway. We created a protein–protein interaction network to analyze the proteins enriched in these pathways. We demonstrated that silencing of TCONS_00029809 remarkably inhibited proliferation, invasion, and migration of BC cells, and accelerated their apoptosis. Conclusions We identified a large number of differentially expressed lncRNAs and mRNAs, which provide data useful in understanding BC carcinogenesis. The lncRNA TCONS_00029809 may be involved in the development of BC.
first_indexed 2024-12-16T11:27:16Z
format Article
id doaj.art-d0ad59733bfa47b39f3a7ca49ec618bd
institution Directory Open Access Journal
issn 1473-2300
language English
last_indexed 2024-12-16T11:27:16Z
publishDate 2021-09-01
publisher SAGE Publishing
record_format Article
series Journal of International Medical Research
spelling doaj.art-d0ad59733bfa47b39f3a7ca49ec618bd2022-12-21T22:33:20ZengSAGE PublishingJournal of International Medical Research1473-23002021-09-014910.1177/0300060520973137Integrated analyses of long noncoding RNAs and mRNAs in the progression of breast cancerJingyun GuoHuining LianMinfeng LiuJianyu DongZhaoze GuoJinlamao YangChangsheng YeObjective The objective was to explore the expression and potential functions of long noncoding RNA (lncRNA) and mRNAs in human breast cancer (BC). Methods Differentially expressed lncRNAs and mRNAs were identified and annotated in BC tissues by using the Agilent human lncRNA assay (Agilent Technologies, Santa Clara, CA, USA) and RNA sequencing. After identification of lncRNAs and mRNAs through quantitative reverse transcription polymerase chain reaction, we conducted a series of functional experiments to confirm the effects of knockdown of one lncRNA, TCONS_00029809, on the progression of BC. Results We discovered 238 lncRNAs and 200 mRNAs that were differentially expressed in BC tissues and para-carcinoma tissue. We showed that differentially expressed mRNAs were related to biological adhesion and biological regulation and mainly enriched in cytokine-cytokine receptor interaction, metabolic pathways, and PI3K-Akt signaling pathway. We created a protein–protein interaction network to analyze the proteins enriched in these pathways. We demonstrated that silencing of TCONS_00029809 remarkably inhibited proliferation, invasion, and migration of BC cells, and accelerated their apoptosis. Conclusions We identified a large number of differentially expressed lncRNAs and mRNAs, which provide data useful in understanding BC carcinogenesis. The lncRNA TCONS_00029809 may be involved in the development of BC.https://doi.org/10.1177/0300060520973137
spellingShingle Jingyun Guo
Huining Lian
Minfeng Liu
Jianyu Dong
Zhaoze Guo
Jinlamao Yang
Changsheng Ye
Integrated analyses of long noncoding RNAs and mRNAs in the progression of breast cancer
Journal of International Medical Research
title Integrated analyses of long noncoding RNAs and mRNAs in the progression of breast cancer
title_full Integrated analyses of long noncoding RNAs and mRNAs in the progression of breast cancer
title_fullStr Integrated analyses of long noncoding RNAs and mRNAs in the progression of breast cancer
title_full_unstemmed Integrated analyses of long noncoding RNAs and mRNAs in the progression of breast cancer
title_short Integrated analyses of long noncoding RNAs and mRNAs in the progression of breast cancer
title_sort integrated analyses of long noncoding rnas and mrnas in the progression of breast cancer
url https://doi.org/10.1177/0300060520973137
work_keys_str_mv AT jingyunguo integratedanalysesoflongnoncodingrnasandmrnasintheprogressionofbreastcancer
AT huininglian integratedanalysesoflongnoncodingrnasandmrnasintheprogressionofbreastcancer
AT minfengliu integratedanalysesoflongnoncodingrnasandmrnasintheprogressionofbreastcancer
AT jianyudong integratedanalysesoflongnoncodingrnasandmrnasintheprogressionofbreastcancer
AT zhaozeguo integratedanalysesoflongnoncodingrnasandmrnasintheprogressionofbreastcancer
AT jinlamaoyang integratedanalysesoflongnoncodingrnasandmrnasintheprogressionofbreastcancer
AT changshengye integratedanalysesoflongnoncodingrnasandmrnasintheprogressionofbreastcancer