Gene network analysis using SWIM reveals interplay between the transcription factor-encoding genes HMGA1, FOXM1, and MYBL2 in triple-negative breast cancer.
Giulia FisconSilvia PegoraroFederica ConteGuidalberto ManfiolettiPaola PaciPublished in: FEBS letters (2021)
Among breast cancer subtypes, triple-negative breast cancer (TNBC) is the most aggressive with the worst prognosis and the highest rates of metastatic disease. To identify TNBC gene signatures, we applied the network-based methodology implemented by the SWIM software to gene expression data of TNBC patients in The Cancer Genome Atlas (TCGA) database. SWIM enables to predict key (switch) genes within the co-expression network, whose perturbations in expression pattern and abundance may contribute to the (patho)biological phenotype. Here, SWIM analysis revealed an interesting interplay between the genes encoding the transcription factors HMGA1, FOXM1, and MYBL2, suggesting a potential cooperation among these three switch genes in TNBC development. The correlative nature of this interplay in TNBC was assessed by in vitro experiments, demonstrating how they may actually modulate the expression of each other.
Keyphrases
- genome wide identification
- genome wide
- transcription factor
- poor prognosis
- network analysis
- dna methylation
- gene expression
- genome wide analysis
- bioinformatics analysis
- copy number
- end stage renal disease
- small cell lung cancer
- newly diagnosed
- chronic kidney disease
- dna binding
- binding protein
- squamous cell carcinoma
- ejection fraction
- papillary thyroid
- young adults
- electronic health record
- patient reported outcomes
- peritoneal dialysis
- squamous cell
- big data
- lymph node metastasis