Annals of Surgical Oncology Cite Track
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Originally published as Ann Surg Oncol Early Release 10.1245/ASO.2004.03.049 on May 18, 2004

Annals of Surgical Oncology 11:560-567 (2004)
© 2004 Society of Surgical Oncology
This Article
Right arrow Full Text
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
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Toth-Fejel, S.
Right arrow Articles by Pommier, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Toth-Fejel, S.
Right arrow Articles by Pommier, R.

ORIGINAL ARTICLES

DNA Fingerprints Provide a Patient-Specific Breast Cancer Marker

SuEllen Toth-Fejel, PhD, Patrick Muller, BS, Bruce Ham, MD, Kevin Esvelt, Nicole Dumas, Kristine Calhoun, MD and Rodney Pommier, MD

From the Division of Surgical Oncology, Department of General Surgery, Oregon Health & Science University, Portland, Oregon.

Correspondence: Address correspondence and reprint requests to: Rodney Pommier, MD, Division of Surgical Oncology, 3181 S. W. Sam Jackson Park Road, Mail Code L223A, Portland, Oregon; Fax: 503-494-7573; e-mail: pommierr{at}ohsu.edu

Background: Detection of systemic breast cancer recurrence is limited by lack of universally expressed tumor cell markers. We hypothesized that a test that detects genetic alterations specific to breast cancer cells of an individual patient would provide a superior cancer marker.

Methods: DNA was extracted from blood, primary tumor, and axillary lymph nodes of 33 breast cancer patients and normal breast tissue of 12 control patients. A patient’s genome was scanned by PCR amplification between Alu sequences. A DNA fingerprint of approximately 17–40 bands was produced for comparison between normal blood and sampled tissues.

Results: There were 7 stage I, 18 stage II, 7 stage III, and 1 stage IV breast cancer cases; 33 of 33 cancer cases showed DNA fingerprint differences between blood and primary tumor (P < .0001).This test predicted 100% of positive nodes. No false-negatives occurred, and in two cases malignancy was detected in histologically negative nodes. Three of the 12 controls showed a single similar band change.

Conclusions: DNA fingerprinting is a method for detecting and characterizing genetic alterations specific to an individual patient’s primary tumor in 100% of cases tested. These specific changes were also identified in 100% of positive nodes, proving the capacity of the test to detect metastases.

Key Words: Alu-PCR • Breast cancer • DNA fingerprinting • Tumor markers







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2004 by the Society of Surgical Oncology.