Toxicological Sciences, Vol 47, 176-180, Copyright © 1999 by Society of Toxicology
IC Ho and TC Lee
In this report, we found that arsenite-resistant human lung adenocarcinoma
cells, CL3R15, were more susceptible to CuCl2 than the parental CL3 cells.
With the aid of atomic absorption spectrophotometry, we observed that
CL3R15 cells accumulated more copper than CL3 cells. We further
demonstrated that sodium arsenite treatment resulted in a dose-dependent
increase of copper accumulation in the parental CL3 cells. In contrast,
copper did not alter the levels of intracellular arsenite in CL3 cells
treated in combination with sodium arsenite and CuCl2. Pretreatment of CL3
cells with sodium arsenite resulted in a significant increase of copper
accumulation and cytotoxicity. These results indicate that intracellular
copper accumulation is enhanced by arsenite. However, arsenite-enhanced
copper accumulation was not observed in two fibroblastic cells, GM00220 and
GM03700, derived from Menkes patients. The Menkes gene encodes a membrane
pump responsible for copper exportation. Our results suggest that Menkes
protein is a potential target of arsenite.
ARTICLES
Sodium arsenite enhances copper accumulation in human lung adenocarcinoma cells
Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan, R.O.C.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
T.-C. Lee, I-C. Ho, W.-J. Lu, and J.-d. Huang Enhanced Expression of Multidrug resistance-associated Protein 2 and Reduced Expression of Aquaglyceroporin 3 in an Arsenic-resistant Human Cell Line J. Biol. Chem., July 7, 2006; 281(27): 18401 - 18407. [Abstract] [Full Text] [PDF] |
||||
