“…In addition, function prediction of SULF1 and CTHRC1 revealed that these proteins were mainly involved in ECM organization and constituent, transmembrane receptor protein serine/threonine kinase, FGF receptor, TGF beta receptor and Wnt receptor signaling pathway, angiogenesis, fibrinolysis, regulation of immune, and VEGF production such as SPARC, COL1A1, COL1A2, COL3A1, COL5A2, COL15A1, ASPN, VCAN, TNFSF4, FAP, POSTN, THBS2, THBS1, SULF2, SULF1, FN1, and LUM. Previous studies have reported that SPARC [37,38], COL1A1, COL1A2 and COL3A1 [39,40], POSTN [41], THBS1 [42], and SULF2 and SULF1 [29] were related to tumor stage and metastasis in GC. Though CTHRC1 had no annotated functions, it shared protein domains with collagen proteins and has been reported to be associated with metastasis in GC [21].…”