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 37, 2950-2956, August 1, 1977]
© 1977 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 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 Sandberg, A. A.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Sandberg, A. A.

Chromosome Markers and Progression in Bladder Cancer1

Avery A. Sandberg

Roswell Park Memorial Institute, Buffalo, New York 14263

The chromosome constitution of 62 papillary tumors and 75 invasive transitional cell carcinomas of the bladder has been examined. Of the 62 papillary tumors, 12 were benign and were found to be preponderantly diploid; 2 of these tumors recurred, however, and in each a few karyotypically abnormal cells were present on the original examination. The modal chromosome number in the 50 papillary cancers ranged in the diploid area (44 to 49 chromosomes) with the karyotypic picture being different from tumor to tumor. Of the 50 papillary cancers, 32 had 1 to 2 marker chromosomes. Twelve of the papillary tumors recurred; only 1 did not have a marker. Thus, the recurrence of the 11 papillary tumors with markers indicates that their presence may be of value in predicting the behavior of papillary cancers of the bladder. The chromosomal picture in the recurrent papillary tumors did not differ materially from the original one, although a slight modification in the chromosome number may occur. On the other hand, invasive transitional cell cancer of the bladder was accompanied by a large number of chromosomes and a relatively large number of marker chromosomes with many complicated karyotypic pictures. The presence of marker chromosomes in papillary cancers may be indicative of the likelihood of recurrence and/or progression of such tumors and should attract the attention of those involved in the care of patients with these cancers.

1 Presented at the National Bladder Cancer Conference, November 28 to December 1, 1976, Miami Beach, Fla. Supported in part by Grant CA-14555 from the National Cancer Institute through the National Bladder Cancer Project.




This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
F. Borel, O. D. Lohez, F. B. Lacroix, and R. L. Margolis
Multiple centrosomes arise from tetraploidy checkpoint failure and mitotic centrosome clusters in p53 and RB pocket protein-compromised cells
PNAS, July 23, 2002; 99(15): 9819 - 9824.
[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 © 1977 by the American Association for Cancer Research.