Cancer Research Infection and Cancer: Biology, Therapeutics, and Prevention
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 53, 4212-4217, September 15, 1993]
© 1993 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 Berg, R. J. W.
Right arrow Articles by van der Leun, J. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Berg, R. J. W.
Right arrow Articles by van der Leun, J. C.

Interaction between Ultraviolet A and Ultraviolet B Radiations in Skin Cancer Induction in Hairless Mice1

Rob J. W. Berg2, Frank R. de Gruijl and Jan C. van der Leun

Institute of Dermatology, University Hospital Utrecht, Post Office Box 85500, 3508 GA Utrecht, The Netherlands

The rate of tumor induction by UV-A radiation rises more slowly with time and accumulated dose than that by UV-B radiation. It has recently been shown that this difference disappears when frank papillomas are excluded from the analysis. Thus, the rate of development of "nonpapillomas" (mainly squamous cell carcinomas and precursors) can be fully characterized by a typical tumor induction time, e.g., the time until 50% of the mice bear tumors. This has opened the possibility to investigate how UV-A and UV-B exposures add up in the induction of squamous cell carcinomas, which is an important issue in risk assessments of artificial UV-A sources for cosmetic or medical purposes.

We present the results of an experiment in which 6 groups of 24 albino SKH:HR1 mice were treated daily for 600 days with either effective UV-A radiation, effective UV-B radiation, or combinations of both. The observed times it took for 50% of the mice to bear tumors in the combination groups were compared with those calculated on the basis of arithmetical addition of effective UV-A and effective UV-B doses. We did not find a statistically significant (P > 0.05) deviation from additivity.

1 Financed by the Dutch Ministry of Welfare, Public Health and Cultural Affairs, Grant RST-89-01.

2 To whom requests for reprints should be addressed.

Received 4/ 9/93. Accepted 7/12/93.




This article has been cited by other articles:


Home page
Cancer Res.Home page
R. J. W. Berg, H. Rebel, G. T. J. van der Horst, H. J. van Kranen, L. H. F. Mullenders, W. A. van Vloten, and F. R. de Gruijl
Impact of Global Genome Repair versus Transcription-coupled Repair on Ultraviolet Carcinogenesis in Hairless Mice
Cancer Res., June 1, 2000; 60(11): 2858 - 2863.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
A. I. Otto, L. Riou, C. Marionnet, T. Mori, A. Sarasin, and T. Magnaldo
Differential Behaviors toward Ultraviolet A and B Radiation of Fibroblasts and Keratinocytes from Normal and DNA-Repair-deficient Patients
Cancer Res., March 1, 1999; 59(6): 1212 - 1218.
[Abstract] [Full Text] [PDF]




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 © 1993 by the American Association for Cancer Research.