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©The Author(s) 2021.
World J Gastroenterol. Aug 14, 2021; 27(30): 4963-4984
Published online Aug 14, 2021. doi: 10.3748/wjg.v27.i30.4963
Published online Aug 14, 2021. doi: 10.3748/wjg.v27.i30.4963
Inhibitor | IC50 CK1 (µmol/L) | Observed effects in cell culture and in vivo data | Ref. |
IC261 | 1.000 ± 0.30 (CK1δ) | Reduced growth of ASPC-1, BxPC3, Capan-1, Colo357, MiaPaCa-2, Panc-1, Panc89, and PancTu-1 at 1.25 µmol/L concentration of IC261; Subcutaneous xenograft model using PancTu-2: reduced tumor size with IC261 or gemcitabine (no synergism with gemcitabine), downregulation of anti-apoptotic genes/upregulation of cell cycle- and cell death-associated regulators; Notable off target effects (affecting the cytoskeleton and ion channels) | [155,168,182-184,202] |
compound 11b | 0.004 ± 0.001 (CK1δ); 0.025 ± 0.004 (CK1ε); 0.010 (p38α) | Cytotoxic effects observed on Colo357 (EC50 = 3.5 ± 0.3 µmol/L) and Panc89 (1.5 ± 0.4 µmol/L) | [174] |
compound 3c | 1.600 (CK1δ/ε) | In a panel of cell lines only effective against Panc-1 (EC50 = 9.3 ± 0.0 µmol/L); Cytotoxic effects observed on A549 (lung carcinoma) and Hek293 (normal cells) significantly higher EC50 values | [175] |
compound 2 | 0.070 ± 0.01 (CK1δkd); 0.520 ± 0.05 (CK1ε) | Cytotoxic effects observed on BxPC3 (EC50 = 0.11 ± 0.01 µmol/L), Colo357 (0.13 ± 0.02 µmol/L), MiaPaCa (0.26 ± 0.02 µmol/L), PancTu-1 (0.70 ± 0.02 µmol/L), and Panc-1 (0.35 ± 0.08 µmol/L); Cell line-specific effects observed in screening against a panel of 82 tumor cell lines | [178] |
IWP-4 | 1.020 ± 0.13 (CK1δ); 7.070 ± 2.01 (CK1ε) | Cytotoxic effects observed on A818-6 (EC50 = 0.93 ± 0.07 µmol/L), MiaPaCa-2 (0.23 ± 0.01 µmol/L), Panc-1 (0.23 ± 0.02 µmol/L), Panc89 (0.58 ± 0.12 µmol/L), and Capan (0.23 ± 0.01 µmol/L); Inhibition of Wnt signaling (Wnt3A overexpression, autocrine/paracrine) with IC50 = 0.71 ± 0.38 µmol/L; Inhibition of Wnt signaling (Wnt3A-conditioned medium, autocrine/paracrine) with EC50 = 1.47 ± 0.55 µmol/L | |
SR-3029 | 0.044 (CK1δ); 0.260 (CK1ε) | Cytotoxic effects observed on Panc-1 (EC50 = 0.023 µmol/L), MiaPaCa2 (0.370 µmol/L), and BxPC3 (0.131 µmol/L); Mouse pharmacokinetic studies with promising results for animal model use of SR-3029; Orthotopic xenograft model using Panc-1, reduced tumor size using SR-3029 and/or gemcitabine (synergism with gemcitabine due to upregulation of dCK) | [152,180] |
- Citation: Traub B, Roth A, Kornmann M, Knippschild U, Bischof J. Stress-activated kinases as therapeutic targets in pancreatic cancer. World J Gastroenterol 2021; 27(30): 4963-4984
- URL: https://www.wjgnet.com/1007-9327/full/v27/i30/4963.htm
- DOI: https://dx.doi.org/10.3748/wjg.v27.i30.4963