SDCBP and ulcer disease: Dissection of the PEA analysis combined with reactome mining emphasized that a set of ten genes (PIK3CA, PIK3CB, PIK3CD, ESR1, KIT, MTOR, HSP90AA1, MAPK1, KDR, and MDM2) were significantly modulated as biological targets to ST-1 as a potent anti-ulcer drug.