Title of article
The growth inhibitory effects of cadmium and copper on the MDA-MB468 human breast cancer cells
Author/Authors
Panjehpour, Mojtaba Department of Clinical Biochemistry - School of Pharmacy, Isfahan Pharmaceutical Sciences Research Center - Isfahan University of Medical Sciences, Isfahan , Taher, Masih-Allah Department of Clinical Biochemistry - School of Pharmacy, Isfahan Pharmaceutical Sciences Research Center - Isfahan University of Medical Sciences, Isfahan , Bayesteh, Mortaza Department of Clinical Biochemistry - School of Pharmacy, Isfahan Pharmaceutical Sciences Research Center - Isfahan University of Medical Sciences, Isfahan
Pages
8
From page
279
To page
286
Abstract
BACKGROUND: Cadmium chloride is an important occupational and environmental pollutant. However, it can also be
anti-carcinogenic under certain conditions. Copper, an essential trace element, has the ability to generate reactive oxygen
species and induce cell apoptosis. This study was aimed to determine the growth inhibitory effects of cadmium and
copper on the MDA-MB468 human breast cancer cells.
METHODS: By using MTT cell viability test, treatment of monolayer cell cultures with different metal concentrations (1-
1000 μM) showed a significant dose dependent decrease (p < 0.05) of viable cells in different times.
RESULTS: A considerable cytotoxicity was observed for CdCl2 at 200 μM and 1 μM after 48 and 72 hours incubations,
respectively. The highest concentration of CuCl2 (1000 μM) had little cytotoxic effects after 48 hours incubation period,
but 1 μM of CuCl2 revealed a considerable cytotoxicity after 72 hours. The maximum synergic cytotoxic effect
was observed at 0.5 μM of both metals.
CONCLUSIONS: The results of the present study indicate that cytotoxic effect of CuCl2 is somehow lesser than that of
CdCl2. This may be due to vital role of copper which is not known for cadmium so far.
Keywords
Trace Elements , Toxicity , Breast Neoplasms , Cadmium , Copper
Journal title
Astroparticle Physics
Serial Year
2010
Record number
2432054
Link To Document