Gene expression trend changes in breast cancer populations over two decades: insights from The Cancer Genome Atlas database

Abstract Background Breast cancer has remained the most common malignancy in women over the past two decades. As lifestyle and living environments have changed, alterations to the disease spectrum have inevitably occurred in this time. As molecular profiling has become a routine diagnostic and objec...

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Main Authors: Jinbo Wu, Hongjun Liu, Taobo Hu, Shu Wang
Format: Article
Language:English
Published: BMC 2022-03-01
Series:Hereditas
Subjects:
Online Access:https://doi.org/10.1186/s41065-022-00230-3
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author Jinbo Wu
Hongjun Liu
Taobo Hu
Shu Wang
author_facet Jinbo Wu
Hongjun Liu
Taobo Hu
Shu Wang
author_sort Jinbo Wu
collection DOAJ
description Abstract Background Breast cancer has remained the most common malignancy in women over the past two decades. As lifestyle and living environments have changed, alterations to the disease spectrum have inevitably occurred in this time. As molecular profiling has become a routine diagnostic and objective indicator of breast cancer etiology, we analyzed changes in gene expression in breast cancer populations over two decades using The Cancer Genome Atlas database. Methods We performed Heatmap and Venn diagram analyses to identify constantly up- and down-regulated genes in breast cancer patients of this cohort. We used Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses to visualize associated functional pathways. Results We determined that three oncogenes, PD-L2, ETV5, and MTOR and 113 long intergenic non-coding RNAs (lincRNAs) were constantly up-regulated, whereas two oncogenes, BCR and GTF2I, one tumor suppression gene MEN1, and 30 lincRNAs were constantly down-regulated. Up-regulated genes were enriched in “focal adhesion” and “PI3K-Akt signaling” pathways, etc., and down-regulated genes were significantly enriched in “metabolic pathways” and “viral myocarditis”. Eight up-regulated genes exhibited doubled or higher expression and the expression of three down-regulated genes was halved or lowered and correlated with long-term survival. Conclusions In this study, we found that gene expression and molecular pathway enrichments are constantly changing with time, importantly, some altered genes were associated with prognostics and are potential therapeutic targets, suggesting that the current molecular subtyping system must be updated to keep pace with this dynamic change.
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spelling doaj.art-6eb9c9b203214478860dfbe4aa0608222022-12-22T02:39:31ZengBMCHereditas1601-52232022-03-01159111110.1186/s41065-022-00230-3Gene expression trend changes in breast cancer populations over two decades: insights from The Cancer Genome Atlas databaseJinbo Wu0Hongjun Liu1Taobo Hu2Shu Wang3Department of Breast Surgery, Peking University People’s HospitalDepartment of Breast Surgery, Peking University People’s HospitalDepartment of Breast Surgery, Peking University People’s HospitalDepartment of Breast Surgery, Peking University People’s HospitalAbstract Background Breast cancer has remained the most common malignancy in women over the past two decades. As lifestyle and living environments have changed, alterations to the disease spectrum have inevitably occurred in this time. As molecular profiling has become a routine diagnostic and objective indicator of breast cancer etiology, we analyzed changes in gene expression in breast cancer populations over two decades using The Cancer Genome Atlas database. Methods We performed Heatmap and Venn diagram analyses to identify constantly up- and down-regulated genes in breast cancer patients of this cohort. We used Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses to visualize associated functional pathways. Results We determined that three oncogenes, PD-L2, ETV5, and MTOR and 113 long intergenic non-coding RNAs (lincRNAs) were constantly up-regulated, whereas two oncogenes, BCR and GTF2I, one tumor suppression gene MEN1, and 30 lincRNAs were constantly down-regulated. Up-regulated genes were enriched in “focal adhesion” and “PI3K-Akt signaling” pathways, etc., and down-regulated genes were significantly enriched in “metabolic pathways” and “viral myocarditis”. Eight up-regulated genes exhibited doubled or higher expression and the expression of three down-regulated genes was halved or lowered and correlated with long-term survival. Conclusions In this study, we found that gene expression and molecular pathway enrichments are constantly changing with time, importantly, some altered genes were associated with prognostics and are potential therapeutic targets, suggesting that the current molecular subtyping system must be updated to keep pace with this dynamic change.https://doi.org/10.1186/s41065-022-00230-3Breast cancerGene expressionTCGA
spellingShingle Jinbo Wu
Hongjun Liu
Taobo Hu
Shu Wang
Gene expression trend changes in breast cancer populations over two decades: insights from The Cancer Genome Atlas database
Hereditas
Breast cancer
Gene expression
TCGA
title Gene expression trend changes in breast cancer populations over two decades: insights from The Cancer Genome Atlas database
title_full Gene expression trend changes in breast cancer populations over two decades: insights from The Cancer Genome Atlas database
title_fullStr Gene expression trend changes in breast cancer populations over two decades: insights from The Cancer Genome Atlas database
title_full_unstemmed Gene expression trend changes in breast cancer populations over two decades: insights from The Cancer Genome Atlas database
title_short Gene expression trend changes in breast cancer populations over two decades: insights from The Cancer Genome Atlas database
title_sort gene expression trend changes in breast cancer populations over two decades insights from the cancer genome atlas database
topic Breast cancer
Gene expression
TCGA
url https://doi.org/10.1186/s41065-022-00230-3
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AT taobohu geneexpressiontrendchangesinbreastcancerpopulationsovertwodecadesinsightsfromthecancergenomeatlasdatabase
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