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. 2022 May 19;12:898563. doi: 10.3389/fonc.2022.898563

Table 2.

GCPDX models as preclinical research tools to evaluate drug efficacy.

Study Type Mice Strain Tumor Location Drug Target (s) Drug (s) Evaluated Observation References
Efficacy NOD/SCID subcutaneous CDK12, PAK2 Procaterol CDK12 and PAK2 as novel therapeutic targets for human gastric cancer (103)
Efficacy Nude subcutaneous RSK2 Carnosol Carnosol is an RSK2 inhibitor for treating gastric cancer (104)
Precision
medicine
Nude subcutaneous c-Met Volitinib Volitinib as a therapeutic option for patients with GC tumors harboring amplified c-Met (105)
Precision
medicine
NSG subcutaneous ERBB2 and MET Afatinib + MET inhibitor  Sensitivity and resistance of trastuzumab-resistant GC cancer to therapy were associated with EGFR/ERBB2 amplification and MET amplification (106)
Precision
medicine
F1: NOD-SCID
Fn: nude
subcutaneous HER2+ HER2 antibody + Herceptin Matching rate of above 80% between original patient tissues and p5 PDX tissues (79)
Efficacy BALB/c nude subcutaneous VEGF, MMP-7, EGFT, Ki-67 and PCNA Trastuzumab + Cetuximab A cancer therapy specific to a stage III GC patient (107)
Efficacy Athymic nude subcutaneous (Matrigel) Wnt/β-catenin target genes (AXIN2, MYC, and LGR5) 2,4-diamino-quinazoline Wnt-signaling pathway is a druggable therapeutic target in the treatment of GC (108)
Efficacy BALB/c nude subcutaneous JAK2/STAT3 CYT997  Inhibiting JAK2/STAT3 pathway is a critical modulator of CYT997-induced autophagy and apoptosis in gastric cancer (109)
Precision
medicine
BALB/c nude subcutaneous (Matrigel) HER2 heterogeneity that is unresponsive to T-DM1 DS-8201a Favoring treatment of HER2 heterogeneous tumors unresponsive to T-DM1 (110)