Table 4.
Test type | Standard anti-cancer drugs |
Cancer types | Cell type/Animal model | Dosage/ concentrations | Signaling pathways (↑upregulation, ↓downregulation) | REF |
---|---|---|---|---|---|---|
in vitro | Cisplatin | Lung cancer | A549/CDDP cells | 100 mg/L | Bax↑, ΔΨm↓, Bcl-2↓, P-gp↓, and PI3K/AKT↓ | (133) |
Colorectal cancer | SW620 cells, SW620/CDDP cells | 1 mg/mL | miR-10b-5p↓ and AGPAT3↑ | (134) | ||
Nasopharyngeal carcinoma | CNE-1 cells | 200 μg/mL | MMP-9↓, p53↑, G0/G1 phase arrest and S phase arrest | (135) | ||
Ovarian cancer | SKOV3 cells | 800 μg/mL | Bcl-2↓, Bax↑, caspase-3↑, and JNK1/2↑ | (136) | ||
Gefitinib | Adenocarcinoma of lung | PC9 cells and HCC827 cells | 200 mg/L | PD-L1/SREBP-1/EMT↓ | (138) | |
Apatinib | Pancreatic cancer | ASPC-1 cells and PANC-1 cells | 200 μg/mL | p-AKT↓, p-ERK↓ and MMP-9↓ | (140) | |
in vivo | Taxol | Breast cancer | 4T1 cells, mouse mononuclear macrophage RAW264.7 and BALB/C mice | 40 mg/kg bw | G2/M phase arrest↓, Taxol-induced cytotoxicity↓ | (139) |
in vitro and in vivo | Cisplatin | Melanoma | A375/CDDP cells, B16/CDDP cells; C57BL/6/SCID mice♂ |
200 mg/kg bw | PD-L1/PI3K/AKT↓ | (132) |
Doxorubicin | Hepatocellular carcinoma | Hep3B cells; BALB/c nude mice♂ |
0-50 mg/L | OGT↓, OGA↑, O-GlcNAcylation↓ | (137) |
Bax, Bcl-2-associated X; ΔΨm, Mitochondrial membrane potential; Bcl-2, B-cell lymphoma-2; PI3K, Phosphatidylinositol-3-kinase; P-gp, P-glycoprotein; AKT, Protein kinase B; Fas, Fas transmembrane glycoprotein; AGPAT3, 1-acylglycerol-3-phosphate O-acyltransferase 3; MMP-9, Matrix metalloproteinase-9; p53, p53 protein; JNK, c-Jun N-terminal kinases1/2; PD-L1, Programmed cell death protein-ligand 1; SREBP1, Recombinant Sterol Regulatory Element Binding Transcription Factor 1; EMT, Epithelial-mesenchymal transition; p-AKT, phospho-Protein kinase B; p-ERK; phospho-Extracellular Regulated Protein Kinases; OGT, O-GlcNAc transferase; OGA, O-GlcNAcase;O-GlcNAcylation, Methods to detect the expression of O-GlcNAc.