Cancer Research The Future of Cancer Research: Science and Patient Impact  Tumor Immunology: New Perspectives
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 57, 1630-1633, May 1, 1997]
© 1997 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 Nagase, S.
Right arrow Articles by Horii, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nagase, S.
Right arrow Articles by Horii, A.

Identification of a 790-kilobase Region of Common Allelic Loss in Chromosome 10q25–q26 in Human Endometrial Cancer1

Satoru Nagase, Hiromitsu Yamakawa, Shinji Sato, Akira Yajima and Akira Horii2

Departments of Molecular Pathology [S. N., H. Y., A. H.] and Obstetrics and Gynecology [S. N., H. Y., S. S., A. Y.], Tohoku University School of Medicine, Sendai, 980-77, Japan

We previously identified two commonly deleted regions on chromosome bands 10q25–q26 in endometrial cancer: an 8-cM region and a 12-cM region. In the present study, we further studied the 8-cM region with 83 endometrial cancer specimens and 14 microsatellite markers and narrowed it down to a 1-cM region between D10S587 and D10S1723. This result was confirmed by two-color fluorescence in situ hybridization analysis. An association between histopathologically lower grade tumor and allelic loss (P = 0.03 by Fisher's exact test) was also observed. We also constructed a yeast artificial chromosome (YAC) contig and found that one YAC clone, which was 790 kb in size, harbored the whole 1-cM region of common allelic loss.

1 This work was supported in part by the Ministry of Education, Science, Sports and Culture of Japan and the Ichiro Kanehara Foundation.

2 To whom requests for reprints should be addressed. Phone: 81-22-717-8042; Fax: 81-22-717-8047; E-mail: horii@mail.cc.tohoku.ac.jp.

Received 1/23/97. Accepted 3/20/97.




This article has been cited by other articles:


Home page
JNCI J Natl Cancer InstHome page
G. L. Mutter, M.-C. Lin, J. T. Fitzgerald, J. B. Kum, J. P. A. Baak, J. A. Lees, L.-P. Weng, and C. Eng
Altered PTEN Expression as a Diagnostic Marker for the Earliest Endometrial Precancers
J Natl Cancer Inst, June 7, 2000; 92(11): 924 - 930.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
L. M. Selfors, J. L. Schutzman, C. Z. Borland, and M. J. Stern
soc-2 encodes a leucine-rich repeat protein implicated in fibroblast growth factor receptor signaling
PNAS, June 9, 1998; 95(12): 6903 - 6908.
[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 © 1997 by the American Association for Cancer Research.