Open AccessAntidesma bunius aqueous crude extract promotes cell death via modulation of redox-sensitive and autophagy associated genes in HCT 116 human-derived colorectal cancer cells
Author(s) -
Sol Joaquin Benigno,
Glenn G. Oyong,
Josafat John Licayan,
Rodolfo Sumayao
Publication year - 2020
Publication title -
archives of biological sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.217
H-Index - 25
eISSN - 1821-4339
pISSN - 0354-4664
DOI - 10.2298/abs200703037b
Subject(s) - oxidative stress , autophagy , viability assay , programmed cell death , biology , cancer cell , atg5 , gene , microbiology and biotechnology , cell , cancer research , cancer , apoptosis , biochemistry , genetics
Antidesma bunius fruit was previously shown to exhibit antioxidant properties, but its anticancer activities remain underexplored. We hypothesized that the phytochemicals in this fruit can influence mitochondrial integrity and can modulate stress-responsive genes in cancer cells. The present study investigated the effects of A. bunius fruit aqueous crude extract (A. bunius ACE) on the viability, redox status, and mitochondrial transmembrane potential (MTP) using a colorectal cancer cell line, HCT 116. The expression of key genes associated with oxidative stress and autophagy was also determined. Treatment of cells with A. bunius ACE resulted in a ~27% reduction in viability, coupled with a marked decrease in oxidative stress index by ~59%. This was accompanied by the upregulation of NRF2 and NRF2-dependent genes. MTP increased ~3-fold in response to A. bunius ACE. The expression of BECLIN1, ATG5, and LC3 genes also increased. Our results indicate that the phytochemicals in A. bunius fruits enhance mitochondrial integrity and modulate the expression of stress-responsive genes, which may be responsible for the mitigation of oxidative stress in cancer cells. These alterations may be involved in the cascade of events leading to cancer cell death effected by A. bunius.