Cinnamaldehyde-Rich Cinnamon Extract Induces Cell Death in Colon Cancer Cell Lines HCT 116 and HT-29.
Arti NileJisoo ShinJuhyun ShinGyun Seok ParkSuhyun LeeJi-Ho LeeKyung-Woo LeeBeob Gyun KimSung-Gu HanRamesh Kumar SainiJae-Wook OhPublished in: International journal of molecular sciences (2023)
Cinnamon is a natural spice with a wide range of pharmacological functions, including anti-microbial, antioxidant, and anti-tumor activities. The aim of this study is to investigate the effects of cinnamaldehyde-rich cinnamon extract (CRCE) on the colorectal cancer cell lines HCT 116 and HT-29. The gas chromatography mass spectrometry analysis of a lipophilic extract of cinnamon revealed the dominance of trans-cinnamaldehyde. Cells treated with CRCE (10-60 µg/mL) showed significantly decreased cell viability in a time- and dose-dependent manner. We also observed that cell proliferation and migration capacity were inhibited in CRCE-treated cells. In addition, a remarkable increase in the number of sub-G 1 -phase cells was observed with arrest at the G 2 phase by CRCE treatment. CRCE also induced mitochondrial stress, and finally, CRCE treatment resulted in activation of apoptotic proteins Caspase-3, -9, and PARP and decreased levels of mu-2-related death-inducing gene protein expression with BH3-interacting domain death agonist (BID) activation.
Keyphrases
- cell cycle arrest
- cell death
- induced apoptosis
- oxidative stress
- gas chromatography mass spectrometry
- anti inflammatory
- endoplasmic reticulum stress
- pi k akt
- single cell
- dna damage
- signaling pathway
- stem cells
- copy number
- genome wide
- gene expression
- cell proliferation
- cell therapy
- mass spectrometry
- replacement therapy
- dna methylation
- heat stress