Background
Colorectal cancer is the second cause of death for tumour worldwide. Among the risk factors for this disease the dietary habits
seem to have a pivotal role. An elevated intake of fats causes a high release in the gut lumen of bile acids that are positively
correlated with colorectal cancer, since they act as detergents and proliferation promoters. Recently, it was evidenced that
bile acids can also be able to induce DNA damage.
Aim of the study
In this study the genotoxicity of deoxycholic acid (DCA) and chenodeoxycholic acid CDCA) has been evaluated in human normal
colonocytes derived from 60 colon biopsies and in tumour cells. The involvement of reactive oxygen species (ROS) and the oxidative
DNA damage was assessed. In addition, the protective effect exerted by both two well-known antioxidants commonly present in
the diet, β-carotene and α-tocopherol, and butyrate which is known to be involved in the regulation of several cellular functions,
has also been tested.
Methods
The DNA damage was evaluated by the “comet assay” or single cell gel electrophoresis (SCGE) both in its conventional use and
by the Endonuclease III modified method, which allow to detect the presence of oxidized pyrimidines.
Results
Bile acids (CDA and CDCA) resulted genotoxic on both normal and tumour human colon cells. The inclusion of the endonuclease
III digestion step in the comet assay demonstrated that bile acids induced an oxidative DNA damage. In addition, treatment
of colonocytes with bile acids in the presence of the antioxidants (β-carotene, α-tocopherol) and Na-butyrate caused a reduction
of DNA damage.
Conclusion
Our results suggest that bile acids may be involved in the tumour initiation by inducing a DNA oxidative damage, and so add
further evidences to the preventive properties of antioxidants present in the Mediterranean diet.
Keywords bile acids - oxidative DNA damage - antioxidants - Na-butyrate - normal colonocytes - tumour cell line