The Chemopreventive Effects of Polyphenols and Coffee, Based upon a DMBA Mouse Model with microRNA and mTOR Gene Expression Biomarkers.
Richard MolnarLaszlo SzaboAndras TomeszArpad DeutschRichard DaragoBence L RaposaNowrasteh GhodratollahTímea VarjasBalazs NemethZsuzsanna OrsosEva PozsgaiJozsef L SzentpeteriFerenc BudanIstvan KissPublished in: Cells (2022)
Polyphenols are capable of decreasing cancer risk. We examined the chemopreventive effects of a green tea ( Camellia sinensis ) extract, polyphenol extract (a mixture of blackberry ( Rubus fruticosus ), blackcurrants ( Ribes nigrum ), and added resveratrol phytoalexin), Chinese bayberry ( Myrica rubra ) extract, and a coffee ( Coffea arabica ) extract on 7,12-dimethylbenz[a]anthracene (DMBA) carcinogen-increased miR-134, miR-132, miR-124-1, miR-9-3, and mTOR gene expressions in the liver, spleen, and kidneys of CBA/Ca mice. The elevation was quenched significantly in the organs, except for miR-132 in the liver of the Chinese bayberry extract-consuming group, and miR-132 in the kidneys of the polyphenol-fed group. In the coffee extract-consuming group, only miR-9-3 and mTOR decreased significantly in the liver; also, miR-134 decreased significantly in the spleen, and, additionally, miR-124-1 decreased significantly in the kidney. Our results are supported by literature data, particularly the DMBA generated ROS-induced inflammatory and proliferative signal transducers, such as TNF, IL1, IL6, and NF-κB; as well as oncogenes, namely RAS and MYC . The examined chemopreventive agents, besides the obvious antioxidant and anti-inflammatory effects, mainly blocked the mentioned DMBA-activated factors and the mitogen-activated protein kinase (MAPK) as well, and, at the same time, induced PTEN as well as SIRT tumor suppressor genes.
Keyphrases
- cell proliferation
- long non coding rna
- oxidative stress
- long noncoding rna
- gene expression
- mouse model
- pi k akt
- systematic review
- signaling pathway
- anti inflammatory
- diabetic rats
- rheumatoid arthritis
- dna damage
- metabolic syndrome
- adipose tissue
- high glucose
- inflammatory response
- endothelial cells
- ischemia reperfusion injury
- drug induced