Table 5.
Summary of the in vivo antineoplastic activities of TBK1 inhibitors
Compounds | Findings | References |
---|---|---|
AMX | Antitumor efficacy in mouse models of melanoma, glioblastoma, pro-B-cell leukemia, prostate cancer, and K-RAS-activated/CTLA4 blockade-resistant lung cancer. AMX and TMZ given in combination display synergism in human glioma cells in xenografts. | [100, 246, 249, 250, 252, 274] |
Compound I | Antitumor capabilities when combined with PD-L1 blockade in mouse models of colorectal carcinoma. | [244, 270] |
GSK8612 | Inhibits HCC development in animal models by attenuating the production of immunosuppressive cytokines, consequently allowing enhanced infiltration of CD8+ T cells into the tumor. | [222] |
MMB | Affords increased survival and decreased spleen size in mouse models of ovarian carcinoma and AML, respectively, and displays synergism with trametinib in suppressing PDA growth in animals. | [231, 275, 276] |
200A | Anticancer activity in mouse models of squamous cell carcinoma. | [244, 270] |