“…In SILAC-DDA MS method, PGAM1, cadherin-3 (CDH3), plasminogen activator urokinase (PLAU), and lunatic fringe (LFNG) were suggested as potential therapeutic target. [123,125] Leukemia inhibitory factor (LIF), LGALS1, TIMP1, ALDH1A1, and GSN were also discovered with therapeutic significance using PRM-based MS and MALDI-TOF MS. [118,124,132,133] Moreover, several proteins, including LGALS3BP, MMP2, CTSD, SERPINE1, BGN, TIMP2, and LGALS1, were identified as potential therapeutic targets, showcasing the proteome complexity in PDAC. [120] In the PTM level, Cao et al [119] uncovered potential therapeutic targets through phosphoproteomics analysis and identified glycoproteins for early detection in PDAC via TMT labeling, including sialyltransferase (ST6GAL1, ST3GAL1), fucosyltransferase (FUT3, FUT11), and galactosyltransferase (B4GALT4, B4GALT1).…”