5-hydroxy-3-6-7-8-3--4--hexamethoxyflavone and Neovascularization--Pathologic

5-hydroxy-3-6-7-8-3--4--hexamethoxyflavone has been researched along with Neovascularization--Pathologic* in 1 studies

Other Studies

1 other study(ies) available for 5-hydroxy-3-6-7-8-3--4--hexamethoxyflavone and Neovascularization--Pathologic

ArticleYear
The inhibitory effects of 5-hydroxy-3,6,7,8,3',4'-hexamethoxyflavone on human colon cancer cells.
    Molecular nutrition & food research, 2011, Volume: 55, Issue:10

    Previously, we reported that 5-hydroxy-3,6,7,8,3',4'-hexamethoxyflavone (5HHMF), a polymethoxyflavone found in citrus peels, potently inhibited the growth of multiple human colon cancer cells. Herein, we further investigated the anti-cancer mechanisms of 5HHMF in human colon cancer cells.. Colony formation assay revealed that 5HHMF dose dependently inhibited colony formation of multiple colon cancer cells. Western blot analysis demonstrated 5HHMF decreased nuclear β-catenin levels and increased the E-cadherin level in a dose-dependent manner. 5HHMF also modified plasma membrane-associated proteins, such as K-Ras, EGFR, and their downstream effectors, such as Akt. Moreover, treatments with 5HHMF inhibited nuclear translocation of NF-κB, which may contribute to its anti-cancer effects. Add-back study showed that the inhibitory effect of 5HHMF was not associated with the production of reactive oxygen species (ROS). In addition, 5HHMF treatment inhibited the capillary tube formation of human umbilical vein endothelial cells (HUVECs) on matrigel, suggesting a potential anti-tumor angiogenesis effect.. Our results demonstrated that 5HHMF suppressed multiple oncogenic molecular events in colon cancer cells.

    Topics: Antineoplastic Agents, Phytogenic; beta Catenin; Cadherins; Cell Line, Tumor; Colonic Neoplasms; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; ErbB Receptors; Flavones; Humans; Membrane Proteins; Neovascularization, Pathologic; NF-kappa B; Oncogene Protein v-akt; Reactive Oxygen Species; Signal Transduction

2011