Chemopreventive and anticarcinogenic effects of BITC and underlying mechanisms of action
Type of cancer explored with phytochemical BITC | Mechanism of action | Results | References |
---|---|---|---|
Breast cancer | Activates the p53-LKB1 and p73-LKB1 axis to intensify p53 signaling and PI3K/AKT/FOXO pathways. Downregulates MMP-2/9 through the signaling pathways PKC and MAPK. Induces apoptosis and G2/M cell cycle arrest. |
Sensitizes tumors to chemotherapy. Demonstrates anticancer effects by activating p53 signaling in breast cancer cells. A study reports that BITC oppresses the mammosphere-constituting efficacy of breast cancer cells. |
[7,37] |
Prostate cancer | Induces apoptosis and G2/M cell cycle arrest. Induces apoptosis in HL-60 cells. |
Promotes apoptosis through the inhibition of several key signaling pathways. | [7,17] |
Colon cancer | Decreases cholesterol levels which inadvertently inhibits the Akt signaling pathway. Inhibits NF-κB DNA binding activity through suppression of MMP-2, MMP-9 and urokinase-plasminogen activator (u-PA). Reduced phosphorylation of JNK1/2, ERK1/2. |
Inhibits human colon cancer cell migration and invasion. | [7,38] |
BITC, benzyl isothiocyanate; p53, tumor protein 53; LKB-1, liver kinase B1; PI3K, phosphoinositide 3-kinase; Akt, protein kinase B; FOXO, forkhead box O; MMP, matrix metalloproteinase; PKC, protein kinase C; MAPK, mitogen-activated protein kinase; HL-60, acute promyelocytic leukemia; JNK, c-Jun N-terminal kinase; ERK, extracellular signal-regulated kinase.