Cancer Research CTRC-AACR San Antonio Breast Cancer Symposium  09 AM Call for Abstracts
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 31, 1496-1505, October 1, 1971]
© 1971 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 Hard, G. C.
Right arrow Articles by Butler, W. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hard, G. C.
Right arrow Articles by Butler, W. H.

Morphogenesis of Epithelial Neoplasms Induced in the Rat Kidney by Dimethylnitrosamine

G. C. Hard1 and W. H. Butler

Medical Research Council Laboratories, Toxicology Unit, Woodmansterne Road, Carshalton, Surrey, England

The sequential changes in tubular epithelium following single i.p. injections of dimethylnitrosamine in carcinogenic doses were followed from 24 hr up to the development of renal adenocarcinomas. The acute changes involved, in particular, the first segment of the proximal tubules, although at higher doses the distal tubules next to glomeruli were also invariably affected. The acute alterations consisted of the formation of lipid droplets and cytosegresomes, the accumulation of granular and membranous debris beneath injured epithelial cells, and sporadic cell necrosis. These changes were associated with a diffuse increase of cells throughout the cortical intertubular space, of which macrophages were the predominant cell type. As the epithelial damage resolved, so did the diffuse mononuclear reaction. Following the acute stage, grossly enlarged nuclei within the convoluted tubules increased in numbers, but their frequency and random distribution suggested that they were unrelated to neoplastic development. From 6 weeks onwards, occasional proliferative lesions were found within tubules located next to glomeruli. Electron microscopic examination revealed that such lesions possessed abnormal brush border formation and nucleoli, which were characteristic features of well-developed adenocarcinomas. Other slower growing proliferative lesions, consisting of hydrated cells, were also described. It was concluded that at least some dimethylnitrosamine-induced renal adenocarcinomas take their origin from the first segment of proximal convoluted tubules.

1 Present address: Baker Medical Research Institute, Commercial Road, Prahran, Victoria 3181, Australia.

Received 3/ 9/71. Accepted 6/ 4/71.




This article has been cited by other articles:


Home page
Toxicol PatholHome page
W. C. Hall, B. Elder, C. L. Walker, S.-L. Cai, D. G. Peters, D. G. Goodman, B. M. Ulland, and J. F. Borzelleca
Spontaneous Renal Tubular Hyperplastic and Neoplastic Lesions in Three Sprague-Dawley Rats from a 90-Day Toxicity Study
Toxicol Pathol, February 1, 2007; 35(2): 233 - 241.
[Abstract] [Full Text] [PDF]


Home page
Toxicol PatholHome page
G. C. Hard and J. C. Seely
Histological Investigation of Diagnostically Challenging Tubule Profiles in Advanced Chronic Progressive Nephropathy (CPN) in the Fischer 344 RaT
Toxicol Pathol, December 1, 2006; 34(7): 941 - 948.
[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 © 1971 by the American Association for Cancer Research.