Hence from the results of these studies, it can be inferred that the differential FOXM1 expression across the different BC subtypes may be associated with the endocrine status of ER, PR and HER2 since FOXM1 overexpression was found to be closely linked with the deprived levels of ER, PR and HER2 status in TNBC. The gene discussed is FOXM1; the disease is breast cancer.