Enriched transcription factor signatures in triple negative breast cancer indicates possible targeted therapies with existing drugs
Year: 2015
Type: article
Abstract: PURPOSE: Triple negative (TN) breast cancers which lack expression of the estrogen (ER), progesterone (PR), and human epidermal growth factor 2 (HER2) receptors convey a poor prognosis due in part to a lack of targeted therapies. METHODS: To identify viable targets for the treatment of TN disease, we have conducted a gene set enrichment analysis (GSEA) on seven different breast cancer whole genome gene expression cohorts comparing TN vs. ER + HER2 - to identify consistently enriched genes that share a common promoter motif. The seven cohorts were profiled on three different genome expression platforms (Affymetrix, Illumina and RNAseq) consisting in total of 2088 samples with IHC metadata. RESULTS: GSEA identified enriched gene expression patterns in TN samples that share common promoter motifs associated with SOX9, E2F1, HIF1A, HMGA1, MYC BACH2, CEBPB, and GCNF/NR6A1. Unexpectedly, NR6A1 an orphan nuclear receptor normally expressed in germ cells of gonads is highly expressed in TN and ER + HER2 - samples making it an ideal drug target. CONCLUSION: With the increasing number of large sample size breast cancer cohorts, an exploratory analysis of genes that are consistently enriched in TN sharing common promoter motifs allows for the identification of possible therapeutic targets with extensive validation in patient derived data sets.
Source: Meta Gene
Language: English
Subfield: Cancer Research
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $2,500
Funders: U.S. Department of Defense, U.S. Department of Health and Human Services, Breast Cancer Research Foundation, American College of Radiology Imaging Network, National Institutes of Health, U.S. Public Health Service, National Cancer Institute, National Center for Advancing Translational Sciences
Awards: G1011812605, G1042980396, Eastern Cooperative Oncology Group, ECOG Statistical Office Data Management Grant, G1422427855, G1431362827, G1771393403, ECOG-ACRIN Network Group Operations Center, CENTER OF EXCELLENCE FOR INDIVIDUALIZATION OF THERAPY FOR BREAST CANCER, G2679961467, Towards identification of prognostic gene sets in breast cancer: The E2197 Trial, G2985072552, G3224512413, G3475623468, G3519244048, G3714277949, G3762168461, G3989676687, G3996959562, G4119534169, G4258443243, G4412485521, G4601003062, G5222394112, G5439978404, G5543746979, G5733733469, G5765316850, G5850682332, G608154585, Clinical and Translational Science Award, G613628225, ECOG-ACRIN Network Group Statistics and Data Management Center, G7117795578, G7137531006, G7495095258, Eastern Cooperative Oncology Group Operations Office, G8313068679, G8653006074, G9000028455, G9000095103, G9000142164, G9000254987, G9000306175, G92717670, G964706321
OpenAlex ID: W333788704
