Exposure to cadmium and copper triggers cytotoxic effects and epigenetic changes in human colorectal carcinoma HT‑29 cells
Author(s) -
Andrada Iftode,
George Drăghici,
Ioana Macașoi,
Iasmina Marcovici,
Dorina Coricovac,
Răzvan Drăgoi,
Alina Andreea Tischer,
Leda Kovatsi,
Aristidis Tsatsakis,
Octavian Creţu,
Cristina Dehelean
Publication year - 2020
Publication title -
experimental and therapeutic medicine
Language(s) - English
Resource type - Journals
eISSN - 1792-1015
pISSN - 1792-0981
DOI - 10.3892/etm.2020.9532
Subject(s) - dna methylation , epigenetics , cytotoxic t cell , methyltransferase , dnmt3b , carcinogenesis , methylation , microbiology and biotechnology , chemistry , dna methyltransferase , oncogene , cadmium , dnmt1 , biology , carcinogen , cancer research , cell cycle , cell , dna , in vitro , gene expression , biochemistry , gene , organic chemistry
Recent scientific evidence suggests a link between epigenetic changes (DNA methylation) and tumorigenesis. Moreover, a potential carcinogenic mechanism of cadmium was associated with changes in DNA methylation. In this study we investigated the impact of CdCl2 and CuSO4 aqueous solutions on DNA methylation in HT-29 cells by quantifying DNA methyltransferase (DNMT1, DNMT3A and DNMT3B) mRNA expression. Furthermore, we also studied the cytotoxic and anti-migratory potential of these substances. The results showed a dose-dependent decrease of viable cell percentage following 24 h of exposure (at concentrations of 0.05; 0.2; 1; 10 and 100 µg/ml), and an inhibitory effect on HT-29 cell migration capacity. In addition, RT-qPCR results showed that cadmium acts as a hypomethylating agent by suppressing DNMT expression, whereas copper acts as a hypermethylating compound by increasing DNMT expression. These findings suggest a cytotoxic potential of both cadmium and copper on HT-29 cells and their capacity to induce epigenetic changes.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom