Cancer Research
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

[Cancer Research 49, 1829-1835, April 1, 1989]
© 1989 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Tveito, G.
Right arrow Articles by Haugen, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tveito, G.
Right arrow Articles by Haugen, A.

Immortalization of Normal Human Kidney Epithelial Cells by Nickel(II)1

Guri Tveito, Inger-Lise Hansteen, Helge Dalen and Aage Haugen2

Department of Toxicology, National Institute of Occupational Health, P. O. Box 8149 Dep, 0033 Oslo 1 [G. T., A. H.]; Department of Occupational Medicine, Telemark Hospital, 3600 Porsgrunn [I-L. H.]; and Laboratory of Clinical Electron Microscopy, University of Bergen, 5021 Bergen [H. D.], Norway

The occupational and environmental hazards of nickel exposure are of great concern in environmental medicine. Nickel workers have increased risk of cancer of the nose, lung, larynx, and possibly the kidney. In the present investigation we have studied the effects of nickel ions on fetal human kidney cortex explants. The explants were continuously exposed to 5 µg/ml NiSO4. After 70–100 days in culture foci of phenotypically altered cells appeared. Immortalized cell lines were established and demonstrated to be of human epithelial origin. Tumorigenicity was not induced, but the cells demonstrated decreased requirement for serum, increased plating efficiency and saturation density, and formation of colonies in soft agar. Chromosome changes in the treated cells were observed. Worth mentioning are change in ploidy (3n) and abnormalities of chromosomes 1, 7, 9, 11, 13, 14 and 20; increased numbers of chromosome 17; and loss of normal chromosomes 20 and 22.

1 This work was supported by the Norwegian Cancer Society.

2 To whom requests for reprints should be addressed.

Received 7/15/88. Revised 11/28/88. Accepted 1/ 4/89.




This article has been cited by other articles:


Home page
J. Am. Soc. Nephrol.Home page
K. Duning, E.-M. Schurek, M. Schluter, M. Bayer, H.-C. Reinhardt, A. Schwab, L. Schaefer, T. Benzing, B. Schermer, M. A. Saleem, et al.
KIBRA Modulates Directional Migration of Podocytes
J. Am. Soc. Nephrol., October 1, 2008; 19(10): 1891 - 1903.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
J. Li, G. Davidson, Y. Huang, B.-H. Jiang, X. Shi, M. Costa, and C. Huang
Nickel Compounds Act through Phosphatidylinositol-3-kinase/Akt-Dependent, p70S6k-Independent Pathway to Induce Hypoxia Inducible Factor Transactivation and Cap43 Expression in Mouse Epidermal Cl41 Cells
Cancer Res., January 1, 2004; 64(1): 94 - 101.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
J. R. Hirsch, N. Skutta, and E. Schlatter
Signaling and distribution of NPR-Bi, the human splice form of the natriuretic peptide receptor type B
Am J Physiol Renal Physiol, August 1, 2003; 285(2): F370 - F374.
[Abstract] [Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
I. CCetinkaya, E. Schlatter, J. R. Hirsch, P. Herter, E. Harms, and R. Kleta
Inhibition of Na+-Dependent Transporters in Cystine-Loaded Human Renal Cells: Electrophysiological Studies on the Fanconi Syndrome of Cystinosis
J. Am. Soc. Nephrol., August 1, 2002; 13(8): 2085 - 2093.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. Sindice, C. Basoglu, A. Cerci, J. R. Hirsch, R. Potthast, M. Kuhn, Y. Ghanekar, S. S. Visweswariah, and E. Schlatter
Guanylin, Uroguanylin, and Heat-stable Euterotoxin Activate Guanylate Cyclase C and/or a Pertussis Toxin-sensitive G Protein in Human Proximal Tubule Cells
J. Biol. Chem., May 10, 2002; 277(20): 17758 - 17764.
[Abstract] [Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
J. R. HIRSCH, M. MEYER, H.-J. MÄGERT, W.-G. FORSSMANN, S. MOLLERUP, P. HERTER, G. WEBER, R. CERMAK, I. ANKORINA-STARK, E. SCHLATTER, et al.
cGMP-Dependent and -Independent Inhibition of a K+ Conductance by Natriuretic Peptides: Molecular and Functional Studies in Human ProximalTubule Cells
J. Am. Soc. Nephrol., March 1, 1999; 10(3): 472 - 480.
[Abstract] [Full Text]


Home page
JNCI J Natl Cancer InstHome page
H.-M. Koo, M. Gray-Goodrich, G. Kohlhagen, M. J. McWilliams, M. Jeffers, A. Vaigro-Wolff, W. G. Alvord, A. Monks, K. D. Paull, Y. Pommier, et al.
The ras Oncogene-Mediated Sensitization of Human Cells to Topoisomerase II Inhibitor-Induced Apoptosis
J Natl Cancer Inst, February 3, 1999; 91(3): 236 - 244.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
H. Hohage, A. Stachon, C. Feidt, J. R. Hirsch, and E. Schlatter
Regulation of Organic Cation Transport in IHKE-1 and LLC-PK1 Cells. Fluorometric Studies with 4-(4-Dimethylaminostyryl)N-methylpyridinium
J. Pharmacol. Exp. Ther., July 1, 1998; 286(1): 305 - 310.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1989 by the American Association for Cancer Research.