The authors stated that daidzein, ursolic acid, apigenin, genistein, and quercetin in the leaf extract strongly inhibited cyclin-dependent kinase 2,6 (CDK2,6), vitamin D3 receptor (VDR), hepatocyte growth factor receptor (MET), epidermal growth factor receptor (EGFR), progesterone receptor (PGR), peroxisome proliferator-activated receptor gamma (PPARG) and interleukin-2 (IL-2) proteins and subsequently blocked tumor proliferation and migration, tumor angiogenesis, tumor adhesion, and degradation of the extracellular matrix. This evidence concerns the gene EGFR and neoplasm.