“…Using this approach and verifying the data using individual gene expression data, we found that AGR2, CEACAM6, GNMT, PDIA2, POSTN, RBPJL, and S100P are upregulated in pancreatic tumor tissue as compared to non-tumor tissue from Black and White patients (Fig 1). The protein products from AGR2 [16,[23][24][25], CEAMAN6 [26][27][28], GNMT [29,30], PDIA2 [31,32], POSTN [17,33,34], RBPJL [35,36] and S100P [37][38][39] have been reported as potential diagnostic and prognostic biomarkers for pancreatic cancer or have demonstrated to be involved in either pancreatic cancer, initiation, migration, invasion, metastasis, or chemoresistance. This report provides additional evidence to support that these genes are specifically upregulated in pancreatic tumor tissue as compared to non-tumor tissue and their products could potentially serve as differentiating biomarkers in pancreatic cancer.…”