Isothiocyanate-Rich Extracts from Cauliflower ( Brassica oleracea Var. Botrytis) and Radish ( Raphanus sativus ) Inhibited Metabolic Activity and Induced ROS in Selected Human HCT116 and HT-29 Colorectal Cancer Cells.
Mardey Liceth Cuellar-NuñezIván Luzardo-OcampoSarah Lee-MartínezMichelle Larrauri-RodríguezGuadalupe Zaldívar-Lelo de LarreaRosa Martha Pérez-SerranoNicolás Camacho-CalderónPublished in: International journal of environmental research and public health (2022)
Cruciferous vegetables such as cauliflower and radish contain isothiocyanates exhibiting chemoprotective effects in vitro and in vivo. This research aimed to assess the impact of cauliflower (CIE) and radish (RIE) isothiocyanate extracts on the metabolic activity, intracellular reactive oxygen species (ROS), and LDH production of selected human colorectal adenocarcinoma cells (HCT116 and HT-29 for early and late colon cancer development, respectively). Non-cancerous colon cells (CCD-33Co) were used as a cytotoxicity control. The CIE samples displayed the highest allyl isothiocyanate (AITC: 12.55 µg/g) contents, whereas RIE was the most abundant in benzyl isothiocyanate (BITC: 15.35 µg/g). Both extracts effectively inhibited HCT116 and HT-29 metabolic activity, but the CIE impact was higher than that of RIE on HCT116 (IC 50 : 0.56 mg/mL). Assays using the half-inhibitory concentrations (IC 50 ) of all treatments, including AITC and BITC, displayed increased ( p < 0.05) LDH (absorbance: 0.25-0.40 nm) and ROS release (1190-1697 relative fluorescence units) in both cell lines. BITC showed the highest in silico binding affinity with all the tested colorectal cancer molecular markers (NF-kB, β-catenin, and NRF2-NFE2). The theoretical evaluation of AITC and BITC bioavailability showed high values for both compounds. The results indicate that CIE and RIE extracts display chemopreventive effects in vitro, but additional experiments are needed to validate their effects.
Keyphrases
- cell cycle arrest
- reactive oxygen species
- cell death
- induced apoptosis
- endothelial cells
- pi k akt
- dna damage
- signaling pathway
- squamous cell carcinoma
- oxidative stress
- epithelial mesenchymal transition
- induced pluripotent stem cells
- immune response
- high throughput
- molecular dynamics simulations
- binding protein
- nuclear factor
- diabetic rats
- pluripotent stem cells
- photodynamic therapy
- quantum dots