» Articles » PMID: 37592220

Aberrant Activation of Five Embryonic Stem Cell-specific Genes Robustly Predicts a High Risk of Relapse in Breast Cancers

Overview
Journal BMC Genomics
Publisher Biomed Central
Specialty Genetics
Date 2023 Aug 17
PMID 37592220
Authors
Affiliations
Soon will be listed here.
Abstract

Background: In breast cancer, as in all cancers, genetic and epigenetic deregulations can result in out-of-context expressions of a set of normally silent tissue-specific genes. The activation of some of these genes in various cancers empowers tumours cells with new properties and drives enhanced proliferation and metastatic activity, leading to a poor survival prognosis.

Results: In this work, we undertook an unprecedented systematic and unbiased analysis of out-of-context activations of a specific set of tissue-specific genes from testis, placenta and embryonic stem cells, not expressed in normal breast tissue as a source of novel prognostic biomarkers. To this end, we combined a strict machine learning framework of transcriptomic data analysis, and successfully created a new robust tool, validated in several independent datasets, which is able to identify patients with a high risk of relapse. This unbiased approach allowed us to identify a panel of five biomarkers, DNMT3B, EXO1, MCM10, CENPF and CENPE, that are robustly and significantly associated with disease-free survival prognosis in breast cancer. Based on these findings, we created a new Gene Expression Classifier (GEC) that stratifies patients. Additionally, thanks to the identified GEC, we were able to paint the specific molecular portraits of the particularly aggressive tumours, which show characteristics of male germ cells, with a particular metabolic gene signature, associated with an enrichment in pro-metastatic and pro-proliferation gene expression.

Conclusions: The GEC classifier is able to reliably identify patients with a high risk of relapse at early stages of the disease. We especially recommend to use the GEC tool for patients with the luminal-A molecular subtype of breast cancer, generally considered of a favourable disease-free survival prognosis, to detect the fraction of patients undergoing a high risk of relapse.

Citing Articles

Identification of immunogenic HLA-A*02:01 epitopes associated with HCC for immunotherapy development.

Maino A, Bourov A-Flin E, Decaens T, Khochbin S, Macek Jilkova Z, Rousseaux S Hepatol Commun. 2025; 9(3).

PMID: 40008881 PMC: 11868434. DOI: 10.1097/HC9.0000000000000659.


A comparative analysis of gene expression profiling by statistical and machine learning approaches.

Bontonou M, Haget A, Boulougouri M, Audit B, Borgnat P, Arbona J Bioinform Adv. 2025; 5(1):vbae199.

PMID: 39897946 PMC: 11783302. DOI: 10.1093/bioadv/vbae199.

References
1.
Gao M, Wang J, Rousseaux S, Tan M, Pan L, Peng L . Metabolically controlled histone H4K5 acylation/acetylation ratio drives BRD4 genomic distribution. Cell Rep. 2021; 36(4):109460. DOI: 10.1016/j.celrep.2021.109460. View

2.
Zhang S, Xie Y, Tian T, Yang Q, Zhou Y, Qiu J . High expression levels of centromere protein A plus upregulation of the phosphatidylinositol 3-kinase/Akt/mammalian target of rapamycin signaling pathway affect chemotherapy response and prognosis in patients with breast cancer. Oncol Lett. 2021; 21(5):410. PMC: 8020387. DOI: 10.3892/ol.2021.12671. View

3.
Morozumi Y, Boussouar F, Tan M, Chaikuad A, Jamshidikia M, Colak G . Atad2 is a generalist facilitator of chromatin dynamics in embryonic stem cells. J Mol Cell Biol. 2015; 8(4):349-62. PMC: 4991664. DOI: 10.1093/jmcb/mjv060. View

4.
Chen H, Wu F, Xu H, Wei G, Ding M, Xu F . Centromere protein F promotes progression of hepatocellular carcinoma through ERK and cell cycle-associated pathways. Cancer Gene Ther. 2021; 29(7):1033-1042. DOI: 10.1038/s41417-021-00404-7. View

5.
Wang J, Mi J, Debernardi A, Vitte A, Emadali A, Meyer J . A six gene expression signature defines aggressive subtypes and predicts outcome in childhood and adult acute lymphoblastic leukemia. Oncotarget. 2015; 6(18):16527-42. PMC: 4599287. DOI: 10.18632/oncotarget.4113. View