Table 4.
Studies on other minor compound effects on cancer and CVDs in the last five years.
Sample | Treatments | Main Results | Ref. |
---|---|---|---|
Human umbilical vein endothelial cells (HUVECs) and dermal microvascular endothelial cells (HMVECs-d-Ad) | Taxifolin (0–50 μM for 18 and 24 h) | Taxifolin inhibits VEGFR-2 signaling pathway. | [77] |
Human breast cancer cells (MDA-MB-231 and MCF7) | AO and MA (0.001–100 μM for 4, 24, 48 and 72 h) | AO inhibits the proliferation and increases the oxidative stress of highly invasive cells. | [114] |
Invasive human breast cancer cells (MDA-MB-231) | UV and ER (0. 001–100 µM for 4, 24, 48 and 72 h) | UV protects DNA from damage, whereas ER enhances damage to DNA. | [115] |
SUM-159 cells subcutaneously injected into athymic nude mice; or into the 2nd right mammary fat pad of female SCID/Beige mice | Pretreatment with DOA (10, 20 μmol/L for 3 d); or graded concentrations of DOA (for 2 h) | DOA blocks the formation of multicellular tumorspheres generated from single-founder stem-like cells in a panel of genetically diverse breast cancer models and suppresses CSC-like states responsible for maintaining tumor initiating cell properties within breast cancer populations. | [116] |