BioMed Research International · 2014 · 17 citations · 32 references
Life SciencesMolecular BiologyOncologyGene ExpressionMolecular OncologyTranscriptomicsCancer Cell SignalingCancer GenomicsCancer TranscriptomicsMolecular Tumor ProfilingOncogenic Signaling PathwaysTranscriptomic ProfilingActin Cytoskeleton RemodelingActin Cytoskeleton ReorganizationBreast Cancer GenomicsBreast Cancer Molecular SubtypesCancer BioinformaticsComparative Cancer Gene Expression ProfilesComparative Cancer Pathway AnalysisMicroarray Analysis
Triple-negative breast cancer (TNBC) is an aggressive type of breast cancer that does not express estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor (Her2/neu). TNBC has worse clinical outcomes than other breast cancer subtypes. However, the key molecules and mechanisms of TNBC migration remain unclear. In this study, we compared two normalized microarray datasets from GEO database between Asian (GSE33926) and non-Asian populations (GSE46581) to determine the molecules and common pathways in TNBC migration. We demonstrated that 16 genes in non-Asian samples and 9 genes in Asian samples are related to TNBC migration. In addition, our analytic results showed that 4 genes, PIK3R3, ITGB1, ITGAL, and ITGA6, were involved in the regulation of actin cytoskeleton. Our results indicated potential genes that link to TNBC migration. This study may help identify novel therapeutic targets for drug development in cancer therapy.
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