TY - JOUR
T1 - Cowpea bean β-vignin-derived AQQSY peptide exerts an anticancer effect by inducing cell cycle arrest in the G0/G1 phase and modulating apoptotic signals
AU - Oliveira Philadelpho, Biane
AU - dos Santos, Johnnie Elton Machado
AU - Elaine Davis, Emily
AU - Barros de Cerqueira e Silva, Mariana
AU - Maffud Cilli, Eduardo
AU - de Souza Ferreira, Ederlan
AU - González de Mejia, Elvira
N1 - This study was financed in part by the Coordena\u00E7\u00E3o de Aperfei\u00E7oamento de Pessoal de N\u00EDvel Superior, Brazil (CAPES), Finance Code 001; FAPESB JCB n\u00B0 0012/2016 and the U.S. Department of Agriculture. The fellowship of Biane Oliveira Philadelpho (FAPESB n\u00B0 BOL0216/2021). Ederlan de Souza Ferreira is a researcher at the CNPq (n\u00B0 301975/2021\u20133). Special thanks to Biorender.com for creating the graphical abstract and Fig. 6 .
PY - 2024/11
Y1 - 2024/11
N2 - The anticancer effect of digested β-vignin and pure peptides from cowpea beans was investigated in cultivated human colon cancer cells. The effect of AQQSY on the cell cycle was similar to that of palbociclib, suggesting that AQQSY may function as a CDK-6-targeting agent. AQQSY peptide reduced the p-Rb/Rb ratio and induced apoptosis through an increase of Bax/Bcl-2 ratio, a decrease of XIAP, and activation of caspase-3. VIPASY peptide showed the potential to induce apoptosis through an increase in Bax/Bcl-2 ratio. The combination of VIPASY and AQQSY with palbociclib caused an additive effect on cell inhibition. Treatment with selected peptides from β-vignin digest caused cell cycle arrest by upregulation of p16 and apoptosis by increasing Bax/Bcl-2 ratio and caspase-8. The peptides and β-vignin digest treatments were more selective for cancer cells than the drugs. Additional research is necessary in vivo to understand the mechanisms of cowpea β-vignin-derived peptides in CRC treatment.
AB - The anticancer effect of digested β-vignin and pure peptides from cowpea beans was investigated in cultivated human colon cancer cells. The effect of AQQSY on the cell cycle was similar to that of palbociclib, suggesting that AQQSY may function as a CDK-6-targeting agent. AQQSY peptide reduced the p-Rb/Rb ratio and induced apoptosis through an increase of Bax/Bcl-2 ratio, a decrease of XIAP, and activation of caspase-3. VIPASY peptide showed the potential to induce apoptosis through an increase in Bax/Bcl-2 ratio. The combination of VIPASY and AQQSY with palbociclib caused an additive effect on cell inhibition. Treatment with selected peptides from β-vignin digest caused cell cycle arrest by upregulation of p16 and apoptosis by increasing Bax/Bcl-2 ratio and caspase-8. The peptides and β-vignin digest treatments were more selective for cancer cells than the drugs. Additional research is necessary in vivo to understand the mechanisms of cowpea β-vignin-derived peptides in CRC treatment.
KW - Bax/Bcl-2. HCT-116 cells
KW - Bioactive peptides
KW - Cell cycle arrest
KW - Docking
KW - Vigna unguiculata
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U2 - 10.1016/j.jff.2024.106498
DO - 10.1016/j.jff.2024.106498
M3 - Article
AN - SCOPUS:85205433759
SN - 1756-4646
VL - 122
JO - Journal of Functional Foods
JF - Journal of Functional Foods
M1 - 106498
ER -