Accession Number:

ADA513453

Title:

Prognostic Significance of Telomere Attrition in Ductal Carcinoma in situ of the Breast

Descriptive Note:

Final rept. 31 Jan 2005-30 Jan 2009

Corporate Author:

NEW MEXICO UNIV HEALTH SCIENCES CENTER ALBUQUERQUE HEALTH SCIENCES CENTER

Personal Author(s):

Report Date:

2009-02-01

Pagination or Media Count:

38.0

Abstract:

We are using an innovative, quantitative assay for telomere DNA content TC developed and characterized by the PI, to test the hypothesis that TC predicts the likelihood of disease recurrence in women with ductal carcinoma in situ DCIS. In Year One, we collaborated to determine whether TC measured in bulk DCIS tumor tissue is comparable to that measured in tumor epithelial cells purified by laser-capture microscopy. In 710 instances, TC in microdissected specimens was 72-112 of that in the undissected control. In Years Two and Three, we confirmed and extended these results in our own laboratory. TC in microdissected samples was compared to TC in unfractionated samples in 1010 instances, TC in the microdissected sample was 75-124 of that in the undissected i.e. bulk control. These results confirm that it is not necessary to microdissect DCIS specimens prior to TC analysis. In Years One-Three, we measured TC in 75 normal breast, 126 DCIS and 657 breast tumor specimens. In Year Two, we used a Kaplan-Meier plot and log-rank test to show that low TC predicts a shorter survival interval. TC was not associated with ethnicity, menopausal status, or the expression of several other markers, including ER, PR, p53, Ki67, and Her2. In Years Three-Four, we demonstrated an association between TC, the extent of allelic imbalance and tumor stage. In Year Four, we obtained longer follow-up to confirm and extend these results. In summary, we have shown that i meaningful TC measurements can be obtained with bulk DCIS tissues, ii TC is associated with tumor stage and iii TC in DCIS is associated with breast cancer-free survival.

Subject Categories:

  • Medicine and Medical Research

Distribution Statement:

APPROVED FOR PUBLIC RELEASE