Non‐oxidized and oxidized flaxseed orbitides differently induce HepG2 cell apoptosis: involvement of cellular uptake and membrane death receptor DR4

Abstract

AbstractBACKGROUNDFlaxseed orbitides have health‐promoting properties, particularly potent anti‐cancer activity. However, flaxseed orbitides containing a methionine structure, such as [1‐9‐NαC]‐linusorb B2 (CLB), are easily oxidized to sulfoxide ([1‐9‐NαC],[1‐Rs,Ss‐MetO]‐linusorb‐B2 (CLC)) and sulfone ([1–9‐NαC], [1‐MetO]‐linusorb B2 (CLK)), with CLC having less anti‐cancer ability than CLB. It is unclear why oxidized flaxseed orbitides are less effective against cancer than non‐oxidized flaxseed orbitide.RESULTSNon‐oxidized ([1‐9‐NαC]‐linusorb‐B3 (CLA) and CLB) and oxidized (CLC and CLK) flaxseed orbitides were found to significantly upregulate the levels of pro‐apoptotic proteins, including Bax/Bcl‐2, CytoC, caspase‐3, and caspase‐8, in a dose‐dependent manner, with non‐oxidized flaxseed orbitides being more effective than oxidized flaxseed orbitides. Mechanically, the cellular absorption of non‐oxidized flaxseed orbitides was higher than that of oxidized flaxseed orbitides. Moreover, the significant fluorescence quenching of DR4 protein by flaxseed orbitides (especially non‐oxidized orbitides) indicated the formation of a DR4–orbitide complex. Molecular docking demonstrated that non‐oxidized orbitides could easily dock into the active cavity of DR4 protein. Further blocking DR4 significantly reduced the ability of non‐oxidized flaxseed orbitides to stimulate caspase‐3 expression, whereas oxidized flaxseed orbitides retained this ability.CONCLUSIONNon‐oxidized flaxseed orbitides are more effective against cancer than oxidized flaxseed orbitides due to higher cellular uptake and activation of the DR4‐mediated death receptor signaling pathway. © 2024 Society of Chemical Industry.