help button home button Am J Pathol Epitomics Buy 2 Antibodies Get 1 Free Special Offer
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Order Full text via Infotrieve
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 Konishi, N.
Right arrow Articles by Nagai, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Konishi, N.
Right arrow Articles by Nagai, H.

American Journal of Pathology, Vol 150, 305-314, Copyright © 1997 by American Society for Investigative Pathology


REGULAR ARTICLES

Different patterns of DNA alterations detected by restriction landmark genomic scanning in heterogeneous prostate carcinomas

N Konishi, Y Hiasa, M Nakamura, Y Kitahori, K Matsubara and H Nagai
Second Department of Pathology, Nara Medical University, Japan.

Alterations in the genomic DNAs of six heterogeneous prostate carcinomas, as well as that of individual and histologically distinct foci within the tumors, were examined using restriction landmark genomic scanning, a method employing two-dimensional gel analysis of a large number of DNA fragments generated by digestion with highly specific endonucleases. Upon autoradiographic imaging, these fragments appear as spots of varying intensity and location specific for each sample. In our study, comparison of cancer DNAs against normal prostate DNA controls yielded alterations in at least 35 spots. Despite differences in the histological grading of tumors, 3 spots common to all tumor samples showed consistent amplification of intensity and 8 other common spots demonstrated consistent reduction of intensity when compared with control. In addition, spot alterations occurred between histologically identical foci isolated from within single tumors. We suggest that these spot changes detected in DNA profiles generated by restriction landmark genomic scanning reflect aberrations in as yet unidentified oncogenes and tumor suppressor genes and indicate that prostate cancer is not only histologically heterogeneous and multifocal but also genetically multicentric.


This article has been cited by other articles:


Home page
Am. J. Pathol.Home page
N. Konishi, M. Nakamura, M. Kishi, M. Nishimine, E. Ishida, and K. Shimada
Heterogeneous Methylation and Deletion Patterns of the INK4a/ARF Locus Within Prostate Carcinomas
Am. J. Pathol., April 1, 2002; 160(4): 1207 - 1214.
[Abstract] [Full Text] [PDF]


Home page
Toxicol PatholHome page
N. Konishi, M. Nakamura, E. Ishida, Y. Kawada, M. Nishimine, H. Nagai, and M. Emi
Specific Genomic Alterations in Rat Renal Cell Carcinomas Induced by N-Ethyl-N-hydroxyethylnitrosamine
Toxicol Pathol, February 1, 2001; 29(2): 232 - 236.
[Abstract] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
D. L. Stoler, N. Chen, M. Basik, M. S. Kahlenberg, M. A. Rodriguez-Bigas, N. J. Petrelli, and G. R. Anderson
The onset and extent of genomic instability in sporadic colorectal tumor progression
PNAS, December 21, 1999; 96(26): 15121 - 15126.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1997 by the American Society for Investigative Pathology.