Anticancer Activity of a Novel High Phenolic Sorghum Bran in Human Colon Cancer Cells.
Seong-Ho LeeJihye LeeThomas HeraldSarah CoxLeela NoronhaRamasamy PerumalHee-Seop LeeDmitriy SmolenskyPublished in: Oxidative medicine and cellular longevity (2020)
Human colon cancer is the third leading cause of mortality in the United States and worldwide. Chemoprevention using diet is widely accepted as a promising approach for cancer management. Numerous population studies indicate a negative correlation between the incidence of colon cancer and consumption of whole grains with a high content of bioactive phenolic compounds. In the current study, we evaluated the anticancer properties of a high phenolic sorghum bran extract prepared using 70% ethanol with 5% citric acid solvent at room temperature. A significant dose-dependent suppression of cell proliferation was observed in human colon cancer cells treated with the high phenolic sorghum bran extract. Apoptosis and S phase growth arrest were induced, while cell migration and invasion were inhibited by this treatment; these effects were accompanied by altered expression of apoptosis, cell cycle, and metastasis-regulating genes. We also found that the high phenolic sorghum bran extract stimulated DNA damage in association with induction of extracellular signal-regulated kinase (ERK) and c-Jun-NH2-terminal kinase (JNK) and subsequent expression of activating transcription factor 3 (ATF3). The present study expands our understanding of the potential use of high phenolic sorghum bran to prevent human colon cancer.
Keyphrases
- risk factors
- cell cycle
- cell proliferation
- endothelial cells
- oxidative stress
- transcription factor
- room temperature
- dna damage
- induced pluripotent stem cells
- poor prognosis
- endoplasmic reticulum stress
- ionic liquid
- single cell
- squamous cell carcinoma
- coronary artery disease
- dna methylation
- risk assessment
- cardiovascular disease
- stem cells
- cardiovascular events
- long non coding rna
- papillary thyroid
- diabetic rats
- lymph node metastasis
- dna repair
- replacement therapy
- bioinformatics analysis