Women diagnosed with triple negative breast cancer can benefit neither from endocrine therapy nor from HER2-targeted therapies (1). We mined published microarray datasets (2, 3) to determine in an unbiased fashion and at the systems level genes most differentially expressed in the primary tumors of patients with breast cancer. We report here significant differential expression of the gene encoding chromosome 20 open reading frame 24, C20orf24, when comparing the tumor cells of patients with

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... le negative breast cancer to normal mammary ductal cells (2). C20orf24 was also differentially expressed in bulk tumor in human breast cancer (3). C20orf24 mRNA was present at significantly increased quantities in TNBC tumor cells relative to normal mammary ductal cells. Analysis of human survival data revealed that expression of C20orf24 in primary tumors of the breast was correlated with overall survival in patients with luminal A type cancer, while within triple negative breast cancer, primary tumor expression of C20orf24 was correlated with overall survival in patients with basal-like 1 and immunomodulatory subtype disease. C20orf24 may be of relevance to initiation, maintenance or progression of triple negative breast cancers.