Short-Term and Long-Term Carcinogenic Effects of Food Contaminants (4-Hydroxynonenal and Pesticides) on Colorectal Human Cells: Involvement of Genotoxic and Non-Genomic Mechanisms.
Liana C ArnaudThierry GauthierAugustin Le NaourSaleha HashimNathalie NaudJerry W ShayFabrice H PierreElisa Boutet-RobinetLaurence HucPublished in: Cancers (2021)
To investigate environmental impacts upon colorectal carcinogenesis (CRC) by diet, we assessed two western diet food contaminants: 4-hydroxynonenal (HNE), a major lipid peroxidation product neoformed during digestion, and a mixture of pesticides. We used human colonic cell lines ectopically eliciting varied genetic susceptibilities to CRC: the non-transformed human epithelial colonic cells (HCECs) and their five isogenic cell lines with the loss of APC (Adenomatous polyposis coli) and TP53 (Tumor protein 53) and/or ectopic expression of mutated KRAS (Kristen-ras). These cell lines have been exposed for either for a short time (2-24 h) or for a long period (3 weeks) to 1 µM HNE and/or 10 µM pesticides. After acute exposure, we did not observe any cytotoxicity or major DNA damage. However, long-term exposure to pesticides alone and in mixture with HNE induced clonogenic transformation in normal HCECs, as well as in cells representing later stages of carcinogenesis. It was associated with genotoxic and non-genomic mechanisms (cell growth, metabolic reprogramming, cell mobility and epithelial-mesenchymal transition) depending on genetic susceptibility. This study demonstrated a potential initiating and promoting effect of food contaminants on CRC after long-term exposure. It supports that these contaminants can accelerate carcinogenesis when mutations in oncogenes or tumor suppressor genes occur.
Keyphrases
- risk assessment
- human health
- induced apoptosis
- endothelial cells
- dna damage
- epithelial mesenchymal transition
- drinking water
- gas chromatography
- copy number
- genome wide
- cell cycle arrest
- weight loss
- physical activity
- high glucose
- poor prognosis
- oxidative stress
- induced pluripotent stem cells
- pluripotent stem cells
- wild type
- signaling pathway
- ulcerative colitis
- binding protein
- endoplasmic reticulum stress
- transforming growth factor
- stem cells
- south africa
- tandem mass spectrometry
- single cell
- gene expression
- cell death
- fatty acid
- protein protein
- dna methylation
- polycyclic aromatic hydrocarbons
- liquid chromatography