The differentially identified pathways include metabolic pathways, proteoglycans in cancer, phagosomes, cell adhesion molecules, fluid shear stress, and atherosclerosis, ubiquitin mediated proteolysis, cardiac muscle contraction, ECM-receptor interaction, p53 signaling pathway, lysine degradation, SNARE interactions in vesicular transport, circadian rhythm, and ribosome. Here, TP53 is linked to atherosclerosis.